+

WO1998050525A1 - Cellules souches provenant du systeme nerveux central adulte et embryonnaire - Google Patents

Cellules souches provenant du systeme nerveux central adulte et embryonnaire Download PDF

Info

Publication number
WO1998050525A1
WO1998050525A1 PCT/US1998/009236 US9809236W WO9850525A1 WO 1998050525 A1 WO1998050525 A1 WO 1998050525A1 US 9809236 W US9809236 W US 9809236W WO 9850525 A1 WO9850525 A1 WO 9850525A1
Authority
WO
WIPO (PCT)
Prior art keywords
cells
neurons
stem cells
culture
cns
Prior art date
Application number
PCT/US1998/009236
Other languages
English (en)
Inventor
Karl K. Johe
Original Assignee
Neuralstem Biopharmaceuticals
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from US08/919,580 external-priority patent/US6040180A/en
Application filed by Neuralstem Biopharmaceuticals filed Critical Neuralstem Biopharmaceuticals
Priority to AU72898/98A priority Critical patent/AU7289898A/en
Priority to EP98920291A priority patent/EP0923640A1/fr
Priority to CA002259484A priority patent/CA2259484A1/fr
Publication of WO1998050525A1 publication Critical patent/WO1998050525A1/fr

Links

Classifications

    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/5005—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells
    • G01N33/5008—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics
    • G01N33/5044—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics involving specific cell types
    • G01N33/5073—Stem cells
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N5/00—Undifferentiated human, animal or plant cells, e.g. cell lines; Tissues; Cultivation or maintenance thereof; Culture media therefor
    • C12N5/06—Animal cells or tissues; Human cells or tissues
    • C12N5/0602—Vertebrate cells
    • C12N5/0618—Cells of the nervous system
    • C12N5/0619—Neurons
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/5005—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells
    • G01N33/5008—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/5005—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells
    • G01N33/5008—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics
    • G01N33/502—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics for testing non-proliferative effects
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/5005—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells
    • G01N33/5008—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics
    • G01N33/5044—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics involving specific cell types
    • G01N33/5058—Neurological cells
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/94—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving narcotics or drugs or pharmaceuticals, neurotransmitters or associated receptors
    • G01N33/9406—Neurotransmitters
    • G01N33/9413—Dopamine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
    • A61K35/12—Materials from mammals; Compositions comprising non-specified tissues or cells; Compositions comprising non-embryonic stem cells; Genetically modified cells
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2506/00—Differentiation of animal cells from one lineage to another; Differentiation of pluripotent cells
    • C12N2506/02—Differentiation of animal cells from one lineage to another; Differentiation of pluripotent cells from embryonic cells
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2510/00—Genetically modified cells
    • C12N2510/02—Cells for production

Definitions

  • the present invention relates to a technology where stem cells from embryonic and adult brain are isolated, propagated, and differentiated efficiently in culture to generate large numbers of nerve cells.
  • This technology for the first time, enables one to generate large numbers of many different kinds of neurons found in a normal brain and provides a new foundation for gene therapy, cell therapy, novel growth factor screening, and drug screening for nervous system disorders.
  • the brain is composed of highly diverse nerve cell types making specific interconnections and, once destroyed, the nerve cells (neurons) do not regenerate.
  • the brain is protected by a blood-brain barrier that effectively blocks the flow of large molecules into the brain, rendering peripheral injection of potential growth factor drugs ineffective.
  • a degenerative disease like Parkinson's
  • the most comprehensive approach to regain a lost neural function may be to replace the damaged cells with healthy cells, rather than just a single gene product.
  • a disease gene i.e., a normal gene
  • This development ideally requires cells of neuronal origin that (1) proliferate in culture to a large number, (2) are amenable to various methods of gene transfer, and (3) integrate and behave as the cells of a normal brain.
  • neurons do not divide and therefore cannot be propagated in culture.
  • various transformed cells of neural and non-neural origins such as glias, fibroblasts, and even muscle cells, which can be proliferated in culture, have been used as possible vehicles for delivering a gene of interest into brain cells.
  • such cells do not and cannot be expected to provide neuronal functions.
  • Another alternative approach has been to force a neural cell of unknown origin to divide in culture by genetically modifying some of its properties, while still retaining some of its ability to become and function as a neuron. Although some "immortalized" cells can display certain features of a neuron, it is unclear whether these altered cells are truly a viable alternative for clinical purposes.
  • a developing fetal brain contains all of the cells germinal to the cells of an adult brain as well as all of the programs necessary to orchestrate them toward the final network of neurons.
  • the nervous system is populated by germinal cells from which all other cells, mainly neurons, astrocytes, and oligodendrocytes, derive during subsequent stages of development.
  • germinal cells that are precursors of the normal brain development would be ideal for all gene-based and cell-based therapies if these germinal cells could be isolated, propagated, and differentiated into mature cell types.
  • the usefulness of the isolated primary cells for both basic research and for therapeutic application depends upon the extent to which the isolated cells resemble those in the brain. Just how many different kinds of precursor cells there are in the developing brain is unknown. However, several distinct cell types may exist: a precursor to neuron only ("committed neuronal progenitor” or "neuroblast " ) , a precursor to oligodendrocyte only (“oligodendroblast”) , a precursor to astrocyte only (“astroblast”) , a bipotential precursor that can become either neuron or oligodendrocyte, neuron or astrocyte, and oligodendrocyte or astrocyte, and a multipotential precursor that maintains the capacity to differentiate into any one of the three cell types.
  • a precursor to neuron only (“committed neuronal progenitor” or "neuroblast " )
  • oligodendroblast oligodendroblast
  • astroblast a precursor to astrocyte only
  • a bipotential precursor that can become either
  • Vicario-Abejon et al used the following . culture conditions which differ from the those described in the present invention: 1. Used enzymatic dissociation, 0.1-0.25% trypsin + 0.4% DNAse I for the initial tissue dissociation as well as subsequent passaging. In the present invention, enzymatic dissociation effectively causes proteolyses of FGF receptors and causes cells to become unresponsive to bFGF and leads to differentiation.
  • bFGF was given only intermittently every 2-3 days, and at 5 ng/ml , less than the optimal concentration disclosed in the present invention. This condition leads to partial differentiation of cells and subsequent heterogeneity of cell types in culture.
  • Basal medium consisting of "N2" components consisted of 5 ng/ml insulin, less than the optimal concentration disclosed in the present invention.
  • the expanded cells under the reported condition are mitotic neurons with antigenic expressions of neurofilament , nestin, neuron-specific enolase, galactocerebroside, and MAP2 (Table I, p. 3604) .
  • the expanding CNS stem cells reported in the present invention express nestin, only, are negative for the above antigens, and are, therefore, a molecularly distinct population of cells from those described by Ray et al.
  • the mitotic "neurons” had a doubling time of 4 days and could be passaged and grown as continuous cell lines.
  • the CNS stem cells double at every 20-24 hours and exhibit a- characteristic regression of mitotic and differentiative capacity over time so that they cannot be maintained as stable cell lines indefinitely.
  • the culture system by Ray et al . generates "nearly pure neuronal cell cultures”.
  • the culture system in the present invention generates multipotential stem cells that can differentiate into all three major cell types of the brain, i.e., neurons, oligodendrocytes, and astrocytes.
  • Embryonic hippocampi were mechanically triturated without the use of an enzyme; however, cells were plated approximately 100,000 cells per cm 2 , optimal for neuronal survival, but almost 10 times higher cell density than optimal for expansion of CNS stem cells. 2.
  • bFGF was given at 20 ng/ml, intermittently, at every 3-4 days.
  • Basal "N2" medium contained 5 ⁇ g/ml insulin, less than optimal. Medium change was also prolonged at every 3-4 days. 4. Cells were passaged by using trypsin.
  • E14-E16 spinal cord was used, a much later stage of development than optimal for stem cells .
  • tissue was dissociated enzymatically by papain and DNase . 3. Initial plating was done in 10% fetal bovine serum.
  • Gage et al report isolation, propagation, and transplantation of cells from adult hippocampus . These mixtures of cells were maintained in culture for one year through multiple passages. 80% of them exhibit rather unusual properties such as co-expressing glial and neuronal antigens while remaining mitotic. These properties are not exhibited by stem cells isolated from the adult striatal subventricular zone.
  • this culture system and the result obtained by Gritti et al . are limited to adult brain where extremely small number of cells were obtained (10 5 cells per brain) and have not been extended to various regions of embryonic brain.
  • the procedure in the present invention permits propagation of stem cells throughout the developing CNS as well as the striatum of the adult brain. It also uses adherent culture and actively avoids cell-cell contact and high cell density. As a result, it permits much more efficient expansion of the cells in an undifferentiated multipotential state and much more precise and efficient control over differentiation of the expanded cells.
  • Reynolds, B. & Weiss, S. Generation of neurons and astrocytes from isolated cells of the adult mammalian central nervous system. Science 255, 1707-1710 (1992) 15 .
  • bFGF regulates the proliferative fate of unipotent (neuronal) and bipotent (neuronal/ astroglial) EGF-generated CNS progenitor cells. Neuron 11, 951-966 (1993) 41 .
  • EGF epidermal growth factor
  • the expanded cells differentiate into neurons and astrocytes, but not into oligodendrocytes, and thus are thought to be a bipotential population, rather than multipotential.
  • Another distinguishing property of the cells is that they respond only to EGF and not to bFGF in particular, whereas CNS stem cells respond similarly to both EGF and bFGF.
  • the sphere culture conditions are not comparable to those employed in the present invention because they require cell aggregation in which many additional undefined interactions are expected to occur.
  • BPNF brain-derived growth factor
  • EGF-generated CNS precursor cells using B27 supplemented medium Exp . Brain Res . 102, 407-414 (1995) 36 .
  • B27 This study utilizes the sphere culture with EGF as described above to test a commercially available medium supplement called "B27". The study simply reports that use of B27 enhances cell survival (not neuronal survival) in a mixed culture containing neurons, astrocytes, and oligodendrocytes.
  • the authors utilize the clonal culture system reported in the above-described reference 43 to test mitogenic efficacy of bFGF and EGF on cortical cells from E10 and E17 embryos. Again, the culture condition applies strictly to microculture in serum containing medium to demonstrate existence of different precursor cells in developing brain. There is no mass expansion, long-term culture, or systematic differentiation protocol.
  • the present invention provides a method for efficiently propagating the undifferentiated germinal cells, i.e., stem cells of the central nervous system (CNS) , in culture and defines conditions to effectively turn the undifferentiated cells into mature cell types.
  • CNS central nervous system
  • These undifferentiated cells or "GNS stem cells” display the multipotential capacity to differentiate into all three major cell types of a mature brain -- neurons, astrocytes, and oligodendrocytes.
  • the same culture conditions enable isolation, expansion, and differentiation of equivalent multipotential cells from the adult brain.
  • Schinstine and Iacovitti 56 reported that some of the astrocytes derived from EGF-generated neural precursor cells expressed neuronal antigens such as tau and MAP2.
  • Qian et al. 57 reported that different concentrations of bFGF proliferate stemlike cells of E10 mouse cortex with varying differentiation potentials ranging from only neuronal to multipotential .
  • Palmer et al. 65 reported that multipotential
  • CNS stem cells could be isolated from adult rat hippocampus. 84% of the cells they expanded, however, co-expressed MAP2c and 04, immature neuronal and oligodendroglial markers. Only 0.2% were MAP2ab positive and less than 0.01% were positive for other neuronal markers such as tau and neurofilament 200. Such properties are quite different from the properties described in the Examples in the present application.
  • Finley et al. 66 reported that the mouse embryonic carcinoma cells line, P19, can form neuronal polarity and be eletrophysiologically active when induced by retinoic acid and serum.
  • Strubing et al . 67 reported that embryonic stem cells grown in serum-containing medium could differentiate into electrophysiologically active neurons in vi tro .
  • Okabe et al . 68 also reported differentiation of some of embryonic stem cells into neurons in vi tro .
  • Gritti et al . 40 reported that multipotential stem cells could be isolated from adult mouse subependyme by EGF and bFGF, which when differentiated, could be eletrophysiologically active and express GABA- , gluatamate-, and ChAT- immunoreactivities, but not others. The frequency of such neurons, however, was not documented and thus it is difficult to ascertain how efficient neuronal maturation was. Moreover, these neuronal phenotypes derived from dividing stem cells were not directly demonstrated by BrdU labeling. This is particularly relevant since aggregate cultures are extremely prone to be contaminated by primary neurons from the tissue, which carry over for several passages. Weiss et al. 49 , in fact, stated that only GABA-positive cells could be obtained from their cultures. Most of the GABA-positive cells may be oligodendrocytes.
  • Results such as these illustrate that identifying CNS stem cells, defining conditions that stably maintain CNS stem cell properties for long-term, and controlling their differentiation into mature cell types are neither obvious nor predictable to those skilled in this art.
  • the present invention discloses an in vi.tro culture of stem cells of the central nervous system of a mammal, a method for the in vi tro culture of the stem cells, and a method for the differentiation of the stem cells.
  • the stem cells maintain the multipotential -capacity to differentiate into neurons, astrocytes, and oligodendrocytes.
  • the stem cells can be derived from central nervous system tissue from a human, fetus or adult.
  • the central nervous system tissue may be hippocampus, cerebral cortex, striatum, septum, diencephalon, mesencephalon, hindbrain, or spinal cord.
  • the stem cells can differentiate to mature neurons exhibiting axon-dendrite polarity, synaptic terminals, and localization of proteins involved in synaptogenesis and synaptic activity including neurotransmitter receptors, transporters, and processing enzymes.
  • the stem cells retain their capacity to generate subtypes of neurons having molecular differences among the subtypes.
  • cells from the central nervous system are : a) dissociated by mechanical trituration; b) plated at the optimal initial density of 1 x 10 6 cells (from hippocampus and septum) or 1.5 x 10 6 cells (from other CNS regions) per 10 cm plate precoated with poly-ornithine and fibronectin; c) cultured in the complete -absence of serum; d) supplied daily with a growth factor selected from the group consisting of i) basic fibroblast growth factor (bFGF) at a concentration of at least 10 ng/ml, ii) EGF at a concentration of at least
  • bFGF basic fibroblast growth factor
  • ng/ml 10 ng/ml, iii) TGF-alpha at a concentration of at least 10 ng/ml, and iv) acidic FGF (aFGF) at a concentration of at least 10 ng/ml plus 1 ⁇ g/ml heparin; e) replaced 100% of culture medium every two days with fresh medium; f) passaged at every 4 days after plating by treating the cultured cells with saline solution and scraping the cells from the plate; and g) replated passaged cells at 0.5 x 10 6 cells per 10 cm plate precoated with poly-ornithine and fibronectin.
  • aFGF acidic FGF
  • the method is applicable with stems cells derived from central nervous system tissue from a human, fetus or adult.
  • the central nervous system tissue may be hippocampus, cerebral cortex, striatum, septum, diencephalon, mesencephalon, hindbrain, or spinal cord.
  • cells from the central nervous system are : a) dissociated by mechanical trituration; b) plated at the optimal initial density of 1 x 10 6 cells (from hippocampus and septum) or 1.5 x 10 6 cells (from other CNS regions) per 10 cm plate precoated with poly-ornithine and fibronectin; c) cultured in the complete absence of serum; d) supplied daily with a growth factor selected from the group consisting of i) basic fibroblast growth factor (bFGF) at a concentration of at least 10 ng/ml, ii) EGF at a concentration of at least 10 ng/ml, iii) TGF-alpha at a concentration of at least 10 ng/ml, and iv) acidic FGF (aFGF) at a concentration of at least 10 ng/ml, ii) EGF at a concentration of at least 10 ng/ml, iii) TGF-alpha at a concentration of at least 10 ng/m
  • differentiation may be specifically directed by adding a second growth factor to the cultured cells either before or after removing the first growth factor from the cultured cells.
  • the second or added growth factor may be platelet-derived growth factor (PDGF) , ciliary neurotropic factor (CNTF) , leukemia inhibitory factor (LIF) , or thyroid hormone, iodothyronine (T3) .
  • the present invention also discloses an in vi tro culture of region-specific, terminally differentiated, mature neurons derived from cultures of mammalian multipotential CNS stem cells and an in vi tro culture method for generation of the differentiated neurons.
  • multipotential CNS stem cells from a specific region are cultured in a chemically defined serum-free culture medium containing a growth factor; the medium is replaced with growth factor-free medium; the stem cells are harvested by trypsinization; plated at a density of between 100,000 to 250,000 cells per square centimeter; and cultured in a glutamic acid-free chemically defined serum-free culture medium.
  • the specific region of the CNS from which the multipotential stems cells are derived are selected from the group consisting of cortex, olfactory tubercle, retina, septum, lateral ganglionic eminence, medial ganglionic eminence, amygdala, hippocampus, thalamus, hypothalamus, ventral and dorsal mesencephalon, brain stem, cerebellum, and spinal cord.
  • the chemically defined serum-free culture medium may be selected from N2 (DMEM/F12, glucose, glutamine, sodium bicarbonate, 25 ⁇ g/ml insulin, 100 ⁇ g/ml human apotransferrin, 25 nM progesterone, 100 ⁇ M putrescine, 30 nM sodium selenite, pH 7.2 8 ) or N2 -modified media.
  • the growth factor may be selected from the group consisting of bFGF, EGF, TGF-alpha and aFGF.
  • the glutamic acid- free chemically defined serum-free culture medium may be supplemented with between 10-10-0 ng/ml of brain-derived neurotropic factor.
  • the method is applicable to multipotential CNS stem cells derived from central nervous system tissue from any mammal, including rat and human.
  • the present invention also discloses- in vi tro cultures of region-specific, terminally differentiated, mature neurons derived from cultures of mammalian multipotential CNS stem cells from a specific region of the CNS.
  • the specific region from which the multipotential stems cells are derived are selected from the group consisting of cortex, olfactory tubercle, retina, septum, lateral ganglionic eminence, medial ganglionic eminence, amygdala, hippocampus, thalamus, hypothalamus, ventral and dorsal mesencephalon, brain stem, cerebellum, and spinal cord.
  • the in vi tro culture of region- specific differentiated neurons may be derived from any mammalian multipotential CNS stem cell, including rat and human.
  • Figure 1A shows the controlled differentiation of CNS stem cells at high density. Rapidly dividing nestin-positive precursor cells were labelled with BrdU during the last 24 hours of proliferation. Pifferentiation was then initiated by withdrawal of bFGF (day 0) and continued for up to 6 days. At indicated times, cells were fixed and stained for BrdU and neuronal antigens. Ratios of cells double-stained for BrdU and each neuronal antigen to total BrdU positive (BrdU+) cells are shown. Up to 50% of BrdU-t- cells expressed neuronal antigens and their expression was time-dependent.
  • MAP2 positive MAP2+
  • TuJl positive TuJl+
  • neurofilament L positive neurofilament L+
  • neurofilament M positive neurofilament . M+
  • Figure IB shows proportions of MAP2+ neurons (•) , GalC+ oligodendrocytes (+) , and GFAP+ astrocytes (o) in differentiated clones.
  • Clones of various sizes ranging from 39 cells to 2800 cells were differentiated for 6 days and analyzed for two cell types per clone by double immunohistochemistry .
  • a partial list is given in Table I and immunostaining shown in Fig. 3. The number of neurons increased with increasing clone size, constituting 50% of the clone.
  • Figure 1C shows a comparison of the mitogenic efficacies of epidermal growth factor (EGF) and basic fibroblast growth factor (bFGF) .
  • EGF epidermal growth factor
  • bFGF basic fibroblast growth factor
  • Figures 2A-P show a typical clone of CNS stem cells. Cells were marked by a circle on the plate within 24 hours of plating before the first mitosis and then expanded up to 10 days (Fig..2A) . Higher magnification view of another clone before differentiation, immunostained with anti-nestin antibody, is shown in Figure 2B. Note the homogeneous radial morphology of the nestin-positive cells consistent with the nestin-positive morphology in neuroepithelium in vivo .
  • Figure 2C shows a sister clone at low magnification, which has been differentiated for 6 days and immunostained with a neuron-specific antibody, TuJl .
  • TuJl-positive neurons Note the widespread and non-localized presence of TuJl-positive neurons across the entire clone. A higher magnification view of the same cells is shown in Figure 2D.
  • the TuJl -positive cells assume typical neuronal morphology. Heterogeneous morphologies in the non-neuronal TuJl-negative cells are apparent.
  • Figures 3A-J show examples of representative clones of embryonic hippocampal cells (3A, 3C, 3E, 3G, 31) and adult subependymal cells (3B, 3D, 3F, 3H, 3J) double-stained with combinations of antibodies to reveal different cell types within individual clones: anti-MAP2, neuronal; anti-GalC, oligodendrocytic; anti-GFAP, astrocytic.
  • the two immunoreactions were developed sequentially and distinguished by using two distinct chromogens via alkaline phosphatase reaction (blue, indicated by arrows) versus horse radish peroxidase reaction (red, indicated by arrow heads) .
  • FIGs 3A and 3B were double-stained with anti-MAP2 (neuronal, arrows) and anti-GFAP (astrocytic, arrow heads) and show that bFGF-expanded clones derived from embryonic or adult brain differentiate into both neurons and astrocytes. (Oligodendrocytes are unstained in this staining.)
  • FIGS 3C and 3D were double-stained with anti-GalC (oligodendrocytic, arrows) and anti-GFAP (astrocytic, arrow heads) and show that bFGF-expanded clones derived from embryonic or adult brain differentiate into both oligodendrocytes and astrocytes. (Neurons are unstained in this staining.)
  • Figures 3E and 3F show clones differentiated in the presence of platelet-derived growth factor (PDGF) .
  • the cells were double stained with anti-MAP2 (neuronal, arrows) and anti-GFAP (astrocytic) . Most cells were MAP2+ and only a few were GFAP+ .
  • Figures 3G and 3H show clones differentiated in the presence of ciliary neurotrophic factor (CNTF) .
  • the cells were double-stained with anti-MAP2 (neuronal) and anti-GFAP (astrocytic, arrow heads) . All cells were intensely GFAP+ .
  • CNTF ciliary neurotrophic factor
  • Figures 31 and 3J show clones differentiated in the presence of thyroid hormone, tri- iodothyronine (T3) .
  • T3 tri- iodothyronine
  • the cells were double-stained with anti-GalC (oligodendrocytic, arrows) and anti-GFAP (astrocytic, arrow heads) .
  • GFAP+ and, particularly, GalC+ cells increased.
  • MAP2+ cells decreased (Table IV) .
  • FIG 4 shows the differentiation of human CNS stem cells into neuron in high density culture.
  • bFGF-expanded CNS cells at high density were differentiated by withdrawal of bFGF ("WD") .
  • the number of neurons expressing tau protein was determined by immunocytochemistry in culture during the expansion phase (“Before WD") versus after differentiation ( "After WD” ) .
  • the dramatic increase in postmitotic neurons only after the withdrawal of bFGF indicates that they were generated from the dividing stem cells.
  • Figures 5A-F show human stem cells stained with human-specific anti-tau antiserum (Chemicon) which identify neurons .
  • Proliferating human CNS stem cells in high density culture do not express tau protein, a neuronal marker ( Figure 5A) .
  • Figure 5B shows tau protein
  • Figure 5B shows that these neurons have indeed derived from dividing stem cells.
  • the stem cells were labeled with 10 ⁇ M bromodeoxyuridine (BrdU) , an indicator of mitosis, for 24 hours just prior to the bFGF withdrawal.
  • FIG. 5C shows a high magnification view of subsequent tau-positive neurons as seen through FITC fluorescence.
  • Figure 5D shows the same field of view as in Figure 5D but seen through rhodamine fluorescence to reveal BrdU-positive nuclei. Most tau-positive neurons are also positive for BrdU, demonstrating that they were derived from mitotic stem cells before the bFGF withdrawal.
  • Figure 5E shows a typical clone at low magnification, which has been expanded from a single cell for 20 days, subsequently differentiated for 12 days, and immunostained with the neuron specific, anti-MAP2 antibody. Neurons are abundant in the clone.
  • Figure 5F shows a higher magnification view of the clone in Figure 5E to indicate that the MAP2 -positive cell are of typical neuronal morphology.
  • Figures 6A-D demonstrate directed differentiation of human CNS stem cells.
  • Human CNS stem cells after 16 days of expansion were grown clonally for an additional 20 days and then differentiated in the presence or absence of single factors, PDGF (10 ng/ml), CNTF (10 ng/ml), or T3 (3 ng/ml) .
  • Figure 6A shows a untreated control clone, with approximately 50% MAP2-positive neurons (arrows) and 2-10% GFAP-positive astrocytes (arrow heads) .
  • Figure 6B shows a PDGF- reated clone, where 75% of cells are MAP2-positive neurons (arrows) and 2-10% GFAP- positive astrocytes (arrow heads) .
  • Figure 6C shows a CNTF-treated clone, where 85% are GFAP-positive astrocytes (arrow heads) and only 9% MAP2 -positive neurons (arrows) .
  • Figure -6D shows a T3 -treated clone with increased number of 04- and/or GalC-positive oligodendrocytes (arrows) and of GFAP -positive astrocytes (arrow heads) .
  • Figures 7A-7I show that a large number of mature neurons with correct axon-dendritic polarity and synaptic activity can be obtained routinely from long-term expanded CNS stem cells. Hippocampal stem cells from E16 rat embryos were expanded in culture for 16 days and through 4 passages.
  • Fig. 7A Neurons stained with TuJl antibody viewed at low magnification (lOOx) to illustrate that production of neurons is efficient.
  • Fig. 7B Typical morphology of neurons revealed by TuJl antibodies (400x) .
  • Fig. 7C Typical morphology of neurons revealed by MAP2 antibodies (400x) .
  • Fig. 7P Neurons stained with synapsin antibody. Only mature neurons containing synaptic vesicles are stained.
  • Fig. 7E BrdU staining . All cells in the culture , neurons and glia , are labeled with BrdU .
  • Fig. 7F Synapsin and BrdU double staining. Mature synapsin-positive cells are also BrdU-positive, demonstrating that they are derived from mitotic stem cells in culture.
  • Fig. 7G Punctate anti-synapsin antibody staining marks the presynaptic axon terminals specifically in large mature neurons.
  • Fig. 7H The synapsin-positive structures are closely apposed to dendritic processes revealed by MAP2 antibody staining.
  • Fig. 71 MAP2 and synapsin proteins are closely associated but not co-localized, suggesting presynaptic-postsynaptic interaction.
  • Figs. 8A-I show that stem cell-derived neurons express various neurotransmitter receptors and transporters expected to be involved in synaptic transmission as detected by RT-PCR.
  • Long-term expanded stem cells derived from E16 rodent cortex were differentiated for 14 days and harvested to prepare RNA. Undifferentiated stem cells were also prepared in order to compare differentiation- specific induction. RNA from a whole brain of adult rat was used as a positive control.
  • Primers specific for NMDA (N-methyl-D-aspartate) and AMPA ( ⁇ -amino-3-hydroxy-5-methyl-4-isoxazole proprionic acid) families of glutamate receptor subtypes as well as for various GABA transporters were used.
  • FIGS 9A-F show examples of typical neurons derived from rat embryonic hippocampal stem cells which had been expanded in vitro for 16 days (approximately 16 cell divisions through 4 passages) and differentiated for 21 days total.
  • Mitotic CNS stem cells were pulse-labeled with bromodeoxyuridine (BrdU) for the last 24 hours prior to differentiation.
  • Resulting neurons were triple-immunostained with antibodies against BrdU (Fig. 9A) , MAP2ab (Fig. 9B) , and synapsin (Fig. 9C) .
  • the composite view of the triple stained cell is shown in Fig. 9P.
  • the BrdU-labeling demonstrates that the differentiated neuron derived from a mitotic precursor in the culture and that it is a terminally differentiated neuron since it retained the mitotic label during the prolonged differentiation phase.
  • MAP2ab is a well-established neuron-specific protein present only in mature neurons and localized mostly in dendrites.
  • Synapsin is a well-established synaptic vesicle protein and thus localizes synaptic terminals in axons .
  • the triple-labeled neurons as shown in Fig.
  • Fig. 9P established that long- term expanded mitotic CNS stem cells terminally differentiate into mature neurons with proper subcellular polarization containing distinct dendritic (post-synaptic) and axonal (presynaptic) structures expected of fully functional neurons.
  • Other synaptic vesicle proteins also localize in the same pattern of punctate axon terminals apposed to soma and dendrites.
  • Fig. 9E and Fig. 9F show another hippocampal CNS stem cell derived mature neuron double-stained for synaptophysin and MAP2ab, respectively.
  • Figure 10 shows a field of neurons from hippocampal CNS stem cells viewed by transmission electron microscopy. The abundant presence of synapses containing synaptic vesicles and post- synaptic densities are evident.
  • FIGs 11 A-P show intracellular electro- physiological recordings from single neurons . obtained from rat E15.5 septal CNS stem cells. Consistent with the morphology, these recordings show that the CNS stem cell-derived neuronal networks are also electrophysiologically active. Thus, when individual cells were stimulated with electrode, they conducted action potentials (Fig. 11A) , demonstrated presence of various voltage-sensitive ion channels (Fig. 11B) , and evoked excitatory and inhibitory postsynaptic potentials in response to bath application of the excitatory neurotransmitter, glutamate (Fig. 11 C and D) . These examples establish beyond doubt that CNS stem cells give rise to terminally differentiated, electrophysiologically functional, neuronal networks . Diverse neuronal phenotypes seen in vivo are obtained from the CNS stem cell cultures. Examples of some of these neuronal phenotypes are shown in Figures 12-18 and Table VII.
  • Figs. 12 A-B show the expression of dopamine receptors Dl and D2 from CNS stem cells isolated from E15.5 lateral and medial ganglionic eminence.
  • Total RNAs were isolated from respective CNS stem cell cultures differentiated for varying periods (0-20 days). Shown is the electrophoresis pattern of the DNA amplified by RT-PCR (reverse transcription-polymerase chain reaction) . Results from five independent culture preparations, run in parallel in a single gel, are shown. The numbers above the lanes indicate the days of differentiation.
  • FIGS 13 A-D show cholinergic neurons from septal CNS stem cells.
  • CNS stem cells derived from E16 septum were differentiated for 18-21 days.
  • the cholinergic neurons were assessed by acetylcholine esterase histochemistry (not shown), by immunostaining for acetylcholine transferase (Fig. 13A) and for acetylcholine transporter (Fig. 13C) .
  • CNS stem cells were incubated with the mitotic label, BrdU (10 ⁇ M) , for 24 hours just before switching to the differentiation condition (Fig. 13B and P) .
  • Figures 14A-F show neuropeptide-containing neurons obtained from rat 15.5 lateral ganglionic eminence (striatum) CNS stem cells. They are a neuropeptide Y-positive (Fig. 14A) , BrdU-positive (Fig. 14B) neuron, a met-enkephalin-positive (Fig. 14C) , BrdU-positive (Fig. 14P) neuron, and a leu- enkephalin-positive (Fig. 14E) , BrdU-positive (Fig. 14F) neuron.
  • Figures 15A-F show typical morphologies of several subtypes of neurons derived from CNS stem cell of rat E12.5 ventral mesencephalon.
  • Figure 15A and B show a TH-positive and BrdU-positive neuron (Fig. 15A-TH staining; Fig. 15B-BrdU staining) .
  • Figure 15 C and P show another TH- positive and MAP2ab-positive neuron (Fig. 15C-TH staining; Fig. 15P-MAP2ab staining) .
  • Figure 15E shows neurons stained with anti-GABA antibody.
  • Figure 15F shows neurons stained by acetylcholine esterase histochemistry.
  • Figures 16A-D show examples of neurons from spinal cord stem cells.
  • Figure 16A shows an acetylcholine esterase-positive neuron derived from rat E13.5 spinal cord CNS stem cells, which is also BrdU-positive (Fig. 16B) .
  • Cholinergic neurons are shown by acetylcholine transferase staining (Fig. 16 C) , which are also BrdU-positive (Fig. 16D) .
  • Figures 17A and B show GABAergic neurons derived from rat E15.5 hippocampal CNS stem cells, which have been double-stained for glutamic acid decarboxylase (Fig. 17A) and GABA (Fig. 17B) .
  • Figure 17C and D show a hippocampal calretinin- positive (Fig. 17C) , MAP2ab-positive (Fig. 17D) neuron.
  • Figures 18A-F show neurons derived from rat E13.5 thalamus and hypothalamus CNS stem cells.
  • Figure 18A shows thalamic neurons stained for tau;
  • Figure 18B shows the same field of view stained for BrdU.
  • Figure 18C shows a hypothalamic neuron stained for tau;
  • Figure 18D shows the same field of view stained for BrdU.
  • Figure 18E and F show synapsin-positive neurons from thalamus and hypothalamus CNS stem cells, respectively.
  • the procedure for isolating, propagating, and differentiating the CNS stem cells are given in detail below.
  • the procedure contains four essential steps that must be followed in concert for successful isolation and differentiation of the CNS stem cells.
  • the four essential steps are as follows: (1) The initial dissociation of cells from tissue is done by mechanical trituration and not by enzymatic digestion. With adult tissue, it is necessary to first enzymatically digest the tissue and then dissociate the cells from the tissue by mechanical trituration.
  • Trituration means gentle agitation of cell aggregates caused by fluid movement occurring during repetitive pipetting action by which individual cells become loose and dissociated from neighboring cells. Trituration is done in a saline solution free of divalent cations whose absence aids break-up of interactions among cell -adhesion proteins on cell surface. Rapidly dividing stem cells in the ventricular zone are only weakly adherent and simply removing the divalent cations from the medium and gentle agitation by pipetting are sufficient to dissociate the tissue into mostly single cells. The cells are then cultured in the complete absence of serum. Even a brief exposure to serum deleteriously affects the differentiation capacity of the stem cells so that they are no longer able to differentiate into neurons and oligodendrocytes. Precoating the plates with poly-L-ornithine and fibronectin facilitates the adhesion of the cells to the plates.
  • the CNS stem cells display an innate property to differentiate spontaneously, which reflects a regulatory mechanism controlling cell cycle depending upon the free concentration of growth factor, the mitogen.
  • the growth factor In order to suppress the differentiation of the stem cells into other cell types and to maintain homogeneity, the growth factor must be supplied daily at a concentration of 10 ng/ml or higher.
  • the growth factor can be selected from (1) basic fibroblast growth factor (bFGF), (2) EGF, (3) TGF-alpha, or (4) acidic FGF (aFGF) . If acidic fibroblast growth factor is selected, heparin at a concentration of 1 ⁇ g/ml must also be supplied.
  • the cells are treated with Hank's buffered saline solution (HBSS) to remove divalent cations in the culture which disrupts the ionic interactions between the cadherins and the integrins on the cell surface and extracellular matrix proteins on the culture plate, causing the cel-ls to round up.
  • HBSS Hank's buffered saline solution
  • Differentiation of the CNS stem cells is achieved by simply removing the mitogen, bFGF or other selected growth factor, from the medium.
  • the cell types i.e., neurons, oligodendrocytes, and astrocytes.
  • the cells In order for the effective controlled differentiation, the cells must be in a homogeneous state which can be achieved by following steps 1-4, above.
  • the isolation of the CNS stem cells in the above-described manner further permits directed differentiation of the cells by treating them with specific growth factors.
  • One practical significance of this directed differentiation to biotechnology is that a single cell type can be enriched in vi tro .
  • PDGF 37 platelet-derived growth factor
  • CNTF ciliary neurotrophic factor
  • T3 thyroid hormone, tri-iodothyronine
  • stem cells to generate neurons, astrocytes, and oligodendrocytes, respectively.
  • Another practical significance, especially for PDGF is that PDGF-induced neurons appear to be actually neuronal progenitors that can further proliferate and expand in culture by PDGF. These cells differentiate only to neurons or to neurons and oligodendrocytes and differ from the stem cells. Isolation of neuronal progenitors from mammalian CNS by PDGF has not been described previously.
  • Rat embryonic hippocampus (gestation day 16; day of conception is day 1, Taconic Farm) were dissected in Hank's buffered saline solution (HBSS) and dissociated by brief mechanical trituration in HBSS.
  • the cells were collected by centrifugation and resuspended in a serum-free medium containing DMEM/F12, glucose, glutamine, sodium bicarbonate, 25 ⁇ g/ml insulin, 100 ⁇ g/ml human apotransferrin, 25 nM progesterone, 100 ⁇ M putrescine, 30 nM sodium selenite, pH 7.2 8 , plus 10 ng/ml recombinant human basic fibroblast growth factor 12 (bFGF; R&D Inc.).
  • bFGF basic fibroblast growth factor 12
  • Cells with multipotential capacity were found throughout the developing neuroepithelium. Under identical culture conditions, similar cells could be prepared from other regions of the developing CNS including cerebral cortex, striatum, septum, diencephalon, mesencephalon, hindbrain, and spinal cord. From E14 cortex and striatum and E16 hippocampus, approximately 70% of acutely dissociated cells responded to bFGF within 2 days of plating by undergoing mitosis.
  • the cells were passaged 4 days after plating during which time cell number increased rapidly with an average cell doubling time of approximately 24 hours. Passaged cells were replated at 0.5 x 10 6 cells per 10 cm plate and were allowed to propagate further. Cells could be passaged up to five times in this manner for a total of 20 days in vi tro during which time a yield of 2 20 cells could be ideally expected. After this time period, the mitotic rate of the cells declined rapidly and the cells gradually lost their multipotential capacity, exhibiting glial characteristics and unable to differentiate into neurons .
  • Differentiation capacity of the cells expanded in mass culture was assessed at each passage by plating 200 cells per 10 cm plate and cultured under conditions as described above. Within 24 hours of plating, well isolated single cells were marked with a 3 mm ring (Nikon) on the bottom of the plate. Initial viability of the marked single cells was 5-10% and each plate typically yielded 10-20 marked clones. Only a single cell resided in each circle. The subsequent population of cells within each circle are progeny of that single cell. Clones were expanded for up to 10 days (500-2000 cells) .
  • Average double time was approximately 24 hours.
  • Antibody reagents used were: anti-nestin antiserum; monoclonal anti-MAP2 (clone HM-2, Sigma) and anti-tau antiserum (Sigma) , monoclonal anti-neurofilament L and M (clones NR4 and NN18, Boehringer-Manheim) , anti-beta tubulin type III (TuJl) , monoclonal anti-GFAP (ICN) , A2B5 (ATCC) , 04, and anti-galactocerebroside (GalC) .
  • clonal density 200 cells per 10 cm plate
  • well-isolated single cells were marked with 3 mm diameter circles. 5-10% of the marked single cells survived and proliferated with a doubling time of 24 hours to generate clones. After various periods of expansion (clone sizes ranging from 2 4 to 2 10 cells) , differentiation of clones was initiated by washing the plates once with HBSS and culturing in the same medium but in the absence of bFGF (Fig. 2) .
  • oligodendrocytes 04+ or GalC+ .
  • Double staining was done sequentially using a commercial kit (Zymed) according to the manufacturer instructions.
  • oligodendrocyte staining cells fixed with 4% paraformaldehyde were stained first for the cell-surface antigens 04 or GalC without permeabilization. The first antibody was developed with alkaline phosphatase reaction (blue) and the second with peroxidase reaction (red) (Zymed) .
  • Neurofilament expression was delayed under these conditions. On average, 8% of the cells in a clone were GalC+ and had typical oligodendrocyte morphology. An additional 8% expressed GFAP and displayed a characteristic astrocytic morphology. The remaining cells were unstained by any of the antibodies specific for differentiated cell types but reacted with A2B5 and/or anti-nestin antibodies. A maximum of 20% of the cells died during differentiation. Identical results were obtained whether clones were obtained from acutely dissociated cells with no prior passage or from cells after 4 passages (26 days in vitro) .
  • Proliferating clones of the multipotential cells contained uniform morphology and patterns of antigen expression. Yet, the separation of neuronal and non-neuronal morphologies occurred rapidly within 24 hours and only after the mitogen withdrawal . The early neurons were evenly distributed throughout the clone without obvious polarity or localization, suggesting the absence of committed neuronal progenitors during clonal expansion. Moreover, the number of neurons increased linearly with increasing clone size and reproducibly constituted 50% of the clone (Fig. IB) .
  • the subependy ⁇ nal layer of adult rat brain contains mitotic nestin positive cells that could be expanded in aggregate culture in the presence of epidermal growth factor (EGF) but not bFGF 15 . Some of the cells in aggregates showed neuronal and astrocytic properties.
  • EGF epidermal growth factor
  • the mitotic population 1% of 1 x 10 s cells/brain
  • bFGF bFGF
  • the cells were dissociated by incubating minced tissues at room temperature for 10 minutes with trypsin (1 mg/ml) , hyaluronidase (0.7 mg/ml), and kynurenic acid (0.2 mg/ml) in oxygenated HBSS. They were washed once in HBSS with 0.7 mg/ml ovomucoid and 0.2 mg/ml kynurenic acid, resuspended, and mechanically triturated in the same solution. Dissociated cells were recovered by centrifugation and cultured in the serum-free medium plus bFGF (10 ng/ml) as described for the embryonic cells.
  • the morphology and growth characteristics of the nestin-positive adult cells were similar to those of embryonic cells. Following bFGF withdrawal, marked clones differentiated into multiple cell types expressing MAP2 , TuJl, GFAP, and GalC (Fig. 3B and D) . Strikingly, the same high proportion of neurons were found in differentiated clones of adult cells as in the embryonic clones (Table III) . More specifically, Table III shows the cell type composition of differentiated clones derived from adult subependymal cells. 23 clones from three independent experiments were quantified.
  • EGF- and bFGF-expanded colonies were also differentiated by withdrawing the mitogens and cell types analyzed as described above. Under the culture conditions of these examples, EGF was an equally effective mitogen as bFGF for adult cells (Fig. 1C) and, when clones were differentiated, they gave rise to all three cell types. EGF-expanded embryonic clones, with and without passage, also differentiated into all three cell types. Unlike the adult cells, however, EGF was at least 10-fold less effective than bFGF as a mitogen for the embryonic cells from several different regions, regardless of initial cell density (Fig. 1C) .
  • TGF ⁇ (10 ng/ml) was also a mitogen for the multipotential cells and was indistinguishable from EGF, while aFGF (10 ng/ml) in the presence of heparin (1 ⁇ g/ml) mimicked the effects of bFGF.
  • the clonal analysis suggests that the multipotential precursors are not committed prior to mitogen withdrawal and thus extracellular signals may regulate cell type determination.
  • PDGF-AA, -AB, or -BB 10 ng/ml CNTF, and 3 ng/ml T3.
  • the cells expressing the neuronal antigens showed a less mature morphology under these conditions.
  • ciliary neurotrophic factor CNTF
  • clones gave rise almost exclusively to astrocytes (Fig. 3G and H, Table IV) .
  • NMTF ciliary neurotrophic factor
  • CNTF-treated cells were intensely GFAP-positive and all showed a flat, astrocytic morphology. LIF showed identical effects as CNTF.
  • Thyroid hormone, tri-iodothyronine (T3) influenced the differentiation of the multipotential precursors toward a mixed glial fate (Fig. 31 and J, Table IV) .
  • Astrocytes and oligodendrocytes were both increased 3 -fold and there was a marked decrease in the proportion of neurons.
  • GalC- and 04 -positive cells showed characteristic oligodendrocyte morphologies.
  • the clones were of similar size in all the experiments and numerical analysis of dead cells showed that- selective cell death cannot account for the changes in the proportion of cell types.
  • Similar results were obtained with multipotential stem cells from embryonic cortex and striatum.
  • the multipotential cells derived from subependymal layer of the adult brain showed quantitatively similar differentiation responses to PDGF, CNTF, and T3 (Fig. 3, Table IV) . This emphasizes the general nature of these pathways .
  • NGF neurotrophic factor
  • NT-3 BDNF
  • TGFbl TGFbl
  • ILlb IL2-11
  • G-CSF G-CSF
  • M-CSF M-CSF
  • GM-CSF oncostatin M
  • stem cell factor erythropoietin
  • interferon gamma 9-cis and all-trans retinoic acid
  • retinyl acetate dexamethasone
  • corticosterone corticosterone
  • Tissues from various regions of human fetal brains were obtained from fetuses of 45 to 114 days of gestation periods. The tissues were dissociated in HBSS by mechanical trituration as described above. Cells were collected by centrifugation, resuspended, plated at 1 x 10 6 cells per 10 cm plate, and expanded in the serum- free medium plus 10 ng/ml bFGF under conditions identical to those described for rodent fetal CNS stem cells above.
  • the capacity to differentiate into one cell type in response to an extracellular signal is the key defining property of rodent CNS stem cells as demonstrated above.
  • the three extracellular , factors, PDGF, CNTF, and T3 also directed the differentiation of the human CNS cell clones in an identical manner (Table V; Fig. 6A-D) .
  • PDGF vascular endothelial growth factor
  • CNTF cellular endothelial growth factor
  • MAP2-positive neuronal cells increased to 71% of a clone, significantly higher than the 46% in the untreated control culture.
  • CNTF MAP2-positive cells decreased and GFAP-positive astrocytes increased dramatically to 85% of the clones.
  • T3 increased 04- or GalC-positive oligodendroglial cells as well as GFAP-positive astroglial cells, while MAP2-positive neurons decreased (Table V) .
  • snapsin proteins found in synaptic vesicles of mature neurons at axon terminals and are involved in exocytosis of neurotransmitters . All four proteins were highly co-localized in the stem cell -derived neurons, in punctate pattern, most likely delineating the axon terminals.
  • the processes bearing the synaptic vesicle proteins were thin, highly elaborate, traveled long distance, and decorated the perimeter of neighboring neurons (Fig. 7G) . They contained axon-specific proteins such as tau and neurofilament and were devoid of dendrite specific proteins such as MAP2a and MAP2b (Fig. 7H and 71) .
  • the stem cell-derived neurons display proper axon-dendrite polarity and exhibit synaptic activity.
  • Stem cell -derived neurons also expressed major neurotransmitter receptors, transporters, and processing enzymes important for neurotransmitter functions. These included members of glutamate receptors, GABA receptors, and dopamine receptors (Fig. 8) .
  • the stem cells retain their capacity to generate subtypes of neurons having molecular differences among the subtypes.
  • predetermined neuroepithelium is at odds with other observations from in vivo fate mapping studies and transplantation studies 5,61"63 .
  • One main conclusion from these experiments is that certain precursor population (s) are multipotential and/or widely plastic in respect to the neuronal versus glial lineages as well as neuronal phenotypes such as neurotransmitter phenotypes and laminar or regional destination.
  • neuronal phenotypes such as neurotransmitter phenotypes and laminar or regional destination.
  • Examples, 1-3, 5 and 6 we limited the differentiation of CNS stem cell clones only to the earliest time point of maturation at which all three cellular phenotypes, i.e., neurons, astrocytes and oligodendrocytes, could be sampled without encountering significant cell death. Hence, neuronal differentiation was limited only to early stages of differentiation. We decided to examine to what extent CNS stem cell-derived neurons could differentiate in vi tro under constitutive conditions, that is, in serum-free, defined minimal medium in the absence of exogenous factors.
  • Neuronal differentiation encompasses many distinct phases of cellular maturation.
  • One of the earliest characteristics of a functional neuron to be expected is the polarization of a neuron into distinct compartments, i.e., soma, dendrite and axon.
  • addition of various commercially available neurotrophic factors including NGF and FGF families could not overcome this barrier.
  • BDNF brain-derived neurotrophic factor
  • CNS stem cells were isolated and expanded under defined conditions as previously described above in Examples 1-3, 5 and 6. Different neurons were derived by isolating CNS stem cells from different regions of the central nervous system and from different stages of the CNS development. Differentiation conditions for obtaining all neuronal phenotypes were identical and different neurons derived only from allowing expression of inherent information already embedded in the expanded CNS stem cells.
  • differentiation was overtly triggered by withdrawal of mitogen, e.g., bFGF, by replacing the growth medium with mitogen-free medium.
  • mitogen e.g., bFGF
  • the cells were harvested by trypsinization and centrifugation according to conventional procedures. Trypsin was inactivated by adding trypsin inhibitor.
  • the resulting cell pellet was resuspended in the same N2 growth medium without bFGF or any other factor and plated at high cell density, optimally at 125,000 cells per square centimeter, onto tissue culture plates precoated with poly-L-ornithine (15 ⁇ g/ml) and fibronectin (1 ⁇ g/ml) or laminin (1 ⁇ g/ml) .
  • tissue culture plates precoated with poly-L-ornithine (15 ⁇ g/ml) and fibronectin (1 ⁇ g/ml) or laminin (1 ⁇ g/ml) .
  • the N2 medium was replaced by N2 medium without glutamic acid.
  • the high cell density was necessary for efficient neuronal differentiation and the absence of glutamic acid was necessary to permit long-term survival of mature neurons .
  • Neurons were maintained for long periods (up to 30 days) under these conditions with the medium changed every 3-4 days. Supplementing the medium with 20 ng/ml of recombinant human BDNF further facilitated neuronal survival and maturation. After 12-30 days of differentiation, cells were fixed with 4% paraformaldehyde and neuronal phenotypes were identified by immunocytochemistry against marker proteins.
  • CNS stem cells from various embryonic brain regions which had been expanded in vi tro for long-term (approximately 16 days and 16 cell divisions through 4 passages) were overtly differentiated for 21 days total as described above.
  • Mitotic CNS stem cells were pulse-labeled with bromodeoxy- uridine (BrdU) for the last 24 to 48 hours prior to differentiation. From all regions, up to 86% of MAP2ab-positive neurons were also positive for BrdU.
  • FIG. 9 are typical neurons derived from rat embryonic hippocampal stem cells. Mature neurons were triple-immunostained with antibodies against BrdU (Fig. 9A) , MAP2ab (Fig. 9B) , and synapsin (Fig. 9C) . Combined staining is shown in Fig. 9P. Figures 9E and F show another typical example of hippocampal stem cell-derived neurons double-stained for synaptophysin (Fig. 9E) , a synaptic vesicle protein labeling axon terminals, and MAP2ab (Fig. 9F) labeling dendritic process.
  • CNS stem cells were isolated from several different regions of rat embryonic CNS at times known to be at the beginning or in the midst of neurogenesis-- embryonic gestation day 15.5 (E 15.5) cortex (CTX) , septum (SEP), lateral ganglionic eminence (LGE) , medial ganglionic eminence (MGE) , hippocampus, E13.5 thalamus, hypothalamus, E12.5 ventral and dorsal mesencephalon, and E11.5-E13.5 spinal cords. From each of these regions, almost homogeneous cultures of CNS stem cells could be expanded for long term (typically for 16 days with average doubling time of 24 hours) according to the culture conditions described previously 64 .
  • Lateral and medial ganglionic eminence are two closely adjacent structures that develop in parallel into striatum and globus pallidus in the adult brain. Popamine receptors, PI and P2 are expressed in striatum, but only P2 is present in pallidus.
  • the expression of PI and P2 receptors from CNS stem cells isolated from -E16 lateral and medial ganglionic eminence was examined by RT-PCR (Fig. 12) . Prior to differentiation, CNS stem cells from either region expressed no dopamine receptors. After 9 days of differentiation, PI and D2 receptors were expressed in LGE-derived stem cells, but only D2 receptor was expressed in cells from MGE. This differential pattern was stable throughout the differentiation course up to 21 days examined (Fig. 12) .
  • FIG. 13A shows a septal CNS stem cell-derived cholinergic neuron immuno-stained for acetylcholine transferase.
  • Figure 13B shows the same field of view as Fig. 13A stained for the mitotic label BrdU.
  • Figure 13C and D show another example of a cholinergic neuron double-stained for vesicular acetylcholine transporter and BrdU, respectively.
  • Table VII summarizes the number of MAP2ab- positive neurons per square centimeter and the proportions of different neuronal phenotypes relative to the total MAP2ab-positive neurons derived from CNS stem cells of several different regions and ages. Approximately 4-5% of the MAP2 positive neurons were cholinergic. In contrast, hippocampal and cortical CNS stem cells gave rise to no cholinergic neurons.
  • LGE and MGE CNS stem cells also expressed vesicular acetylcholine transporter, a specific marker of cholinergic neurons (Table VII) .
  • Figures 14A, C, and D show typical LGE CNS stem cell -derived neurons stained for neuropeptide Y, met-enkephalin, and leu- enkephalin, respectively.
  • Figures 14B, D, and F show the immunostaining for BrdU of the same fields as in Figs. 14A, C, and E, respectively.
  • FIG. 15A shows a typical CNS stem cell derived TH-positive neuron and Figure 15B shows the corresponding BrdU staining of the same field. All TH-positive cells are neurons as shown by double-staining for TH and MAP2ab (Figs. 15C and D, respectively) . Most of the remaining neurons were positive for the marker of GABAergic neurons, glutamic acid decarboxylase (GAD) as well as for GABA itself (Fig. 15E) and/or for acetylcholine esterase (Fig. 15F; Table VII) which is known to be expressed in monoaminergic neurons in this area.
  • GABAergic neurons glutamic acid decarboxylase
  • Fig. 15E glutamic acid decarboxylase
  • Fig. 15F acetylcholine esterase
  • CNS stem cells derived from dorsal mesencephalon in contrast, generated no TH-positive neurons (Table VII) . Almost all neurons of this area (100.9 ⁇ 9.1%) expressed acetylcholine esterase (Table VII) . They are most likely monoaminergic neurons, consistent with the in vivo pattern. Significantly, no TH-positive neurons arose from CNS stem cells derived from cortex, septum, hippocampus, striatum, and spinal cord (Table VII) . Thus, in parallel with the known in vivo expression pattern, generation of TH-positive neurons were unique to ventral mesencephalon CNS stem cells in vi tro .
  • CNS stem cells from E13.5 cervical and thoracic spinal cords were expanded and differentiated.
  • 1.2 ⁇ 0.1% of MAP2 positive neurons were cholinergic containing vesicular acetylcholine transporter (Table VII) .
  • Cholinergic neurons also expressing acetylcholine transferase and BrdU-positive are shown in Figures 16C and D, respectively.
  • a typical acetylcholine esterase- positive and BrdU-positive neuron is shown in Figure 16A and B, respectively.
  • Neurons derived from E15.5 hippocampal and cortical CNS stem cells did not express tyrosine hydroxylase, acetylcholine esterase, acetylcholine transferase, and vesicular acetylcholine transporter (Table VII) . This is appropriate for known absence of these markers in hippocampus in vivo .
  • About 30% of MAP2ab-positive neurons were GABAergic, indicated by expression of GAD and GABA.
  • Figures 17A and B show typical examples of GAD- and GABA-positive staining, respectively, which completely overlap.
  • a typical hippocampal calretinin- and MAP2ab-positive neuron is shown in Figures 17C and D, respectively.
  • Mature neurons can be also be derived with equal efficiency from E13.5 thalamus and hypothalamus. These neurons contain exceptionally long axonal processes.
  • a typical thalamic neuron stained for the axonal protein, tau, and BrdU is shown in Figures 18A and B, respectively.
  • a typical hypothalamic neuron stained for tau and BrdU is shown in Figures 18C and D-, respectively.
  • Synapsin staining of thalamic and hypothalamic neurons is shown in Figures 18E and F, respectively.
  • neurons and the CNS stem cells capable of differentiating into such neurons provide the key element for gene therapy, cell therapy, and identification of novel therapeutic molecules (proteins, peptides, DNA, oligonucleotides, synthetic and natural organic compounds) directed to nervous system disorders.
  • the multipotential cells could be efficiently isolated from many regions of the developing CNS, indicating that they are abundant throughout the neuroepithelium. This contrasts with the widely-held notion that stem cells are rare. Differentiation of the stem cells can be effectively directed by extracellular factors that are known to be present during CNS development 16"23 . This suggests that different extracellular factors can act on a single class of stem cells to generate different cell types. A similar instructive mechanism has also been observed in vi tro with stem cells isolated from the peripheral nervous system 24 .
  • Another mechanism of fate choice regulation in vivo may involve intermediate stages of differentiation. Identification of the bipotential oligodendrocyte precursor cell, 0-2A, from postnatal optic nerve directly demonstrated that restricted progenitors are produced during development 25,26 .
  • the stem cells are distinct from the 0-2A cells. Their origins, properties, and developmental capacities differ. Given that the stem cells differentiate into oligodendrocytes, the differentiation pathway may involve an obligatory intermediate stage, a committed progenitor state like the 0-2A cell. The similar responses of both cells to T3 and CNTF 27,28 may reflect this common step.
  • the homogeneous stem cell culture can be triggered to differentiate under precisely controlled conditions where up to 50% of the cells differentiate into neurons while the remaining cells become astrocytes and oligodendrocytes;
  • growth factors have been identified that effectively direct the stem cells to differentiate into a single cell type, i.e., neuron, astrocyte, or oligodendrocyte;
  • this CNS stem cell technology permits large scale culture of homogeneous stem cells in an undifferentiated state. The longer that the cells can be maintained in the stem cell state, the higher the yield of neurons that can be derived from the culture, thereby enabling more efficient gene transfer and large scale selection of those cells carrying the gene of interest.
  • this culture system permits controlled differentiation of the stem cells where 50% of the expanded cells now turn into neurons. This efficient differentiation, combined with efficient proliferation, routinely yields more than 100 million neurons from the neocortex of one rat fetal brain in a two-week period.
  • the differentiation of- the stem cells into neurons, astrocytes, and oligodendrocytes occurs constitutively where all three cell types continue to mature in culture, most likely due to nurturing interactions with each other, as during normal brain development.
  • Many different types of neurons arise, which respond to many growth factors and contain neurotransmitters and their receptors.
  • a significant portion of the brain development can be recapitulated in a manipulable environment, thereby highlighting the potential to extract and test novel neurotropic factors normally secreted by these cells.
  • these results permit the establishment of conditions by which dividing immature neurons can be derived directly from the stem cells and expanded further to allow large scale isolation of specific kinds of neurons in culture .
  • the stem cell technology of the present . invention can be developed for direct application to many different aspects of therapy and drug discovery for nervous system disorders. Outlined below are four examples for potential commercial applications, i.e., gene therapy for Parkinson's disease, cell therapy, search for novel growth factors, and assays for drug screening.
  • the CNS stem cells more than meet the technical criteria as vehicles for gene therapies and cell therapies in general.
  • the stem cells can be expanded rapidly under precisely controlled, reproducible conditions. Furthermore, these cells are readily accessible to all standard gene transfer protocols such as via retroviruses, adenoviruses, liposomes, and calcium phosphate treatment, as well as subsequent selection and expansion protocols.
  • the expanded stem cells efficiently differentiate into neurons en masse .
  • stem cells make them unique as the fundamental basis of therapeutic development directed at the human nervous system.
  • stem cells once stem cells are triggered to differentiate into mature cell types, all of the molecular interactions are in place within the culture system to generate, to mature, and to survive a variety of different cell types and neuronal subtypes. These interactions recapitulate a significant portion of the natural brain development process. Therefore, the stem cells, as vehicles of gene therapy and cell therapy, refurnish not only a single potential gene or factor to be delivered but also the whole infrastructure for nerve regeneration.
  • the stem cells in cul-ture are expanded from the multipotential germinal precursors of the normal brain development .
  • these stem cells retain the capacity to become not only three different cell types but also many different types of neurons depending upon the environmental cues to which they are exposed.
  • This broad plasticity which is the inherent property of the stem cells, distinctly suggests that, once transplanted, the cells may retain the capacity to conform to many different host brain regions and to differentiate into neurons specific for that particular host region.
  • These intrinsic properties of the primary stem cells are far different from the existing tumorigenic cell lines where some neuronal differentiation can be induced under artificial conditions. Therefore, with these unique properties, the expandable human CNS stem cells contain significant commercial potential by themselves with little further development.
  • Parkinson's Disease results mainly from degeneration of dopamine releasing neurons in the substantia nigra of the brain and the resulting depletion of dopamine neurotransmitter in the striatum.
  • the cause of this degeneration is unknown but the motor degeneration symptoms of the disease can be alleviated by peripherally administering the dopamine precursor, L-dopa, at the early onset of the disease.
  • L-dopa is no longer effective and currently no further treatment is available.
  • One promising treatment being developed is to transplant dopamine-rich substantia nigra neurons from fetal brain into the striatum of the brain of the patient. Results obtained from various clinical centers look extremely optimistic.
  • Tyrosine hydroxylase is the key enzyme for dopamine synthesis.
  • Human CNS stem cells derived from fetal basal ganglia can be produced which express the tyrosine hydroxylase (TH) gene. These cells can be expanded, differentiated, and transplanted into the patient's striatum. Since the cells are originally derived from the primordial striatum, they would have the best chance of integrating into this region of the brain. Production of such cells and their successful transplantation into animal models will result in the most promising application of gene therapy to date.
  • CNS stem cells are the natural germinal cells of the developing brain with the capacity to become the cells of the mature brain, the stem cells from the spinal cord and different regions of the brain may be used directly to repopulate degenerated nerves in various neuropathies .
  • Drug discovery by traditional pharmacology had been performed without the knowledge of such complexity using whole brain homogenate and animals, and mostly produced analogs of neurotransmitters with broad actions and side effects.
  • the next generation of pharmaceutical drugs aimed to modify specific brain functions may be obtained by screening potential- chemicals against neurons displaying a specific profile of neurotransmitters, receptors complexes, and ion channels.
  • CNS stem cells expanded and differentiated into neurons in culture express several neurotransmitters and receptor complexes .
  • Many cell lines derived from stem cells and neuronal progenitors of different regions of the brain can be developed which, when differentiated into mature neurons, would display a unique profile of neurotransmitter receptor complexes .
  • Such neuronal cell lines will be valuable tools for designing and screening potential drugs.
  • the CNS stem cell technology of this application offers broad and significant potentials for treating nervous system disorders. The following scientific articles have been cited throughout this application. 1. Turner, D.L. & Cepko, C.L., Nature 328,
  • 01igodendrocytes (04+/Galc+) 2.6+0.8 0.8+0.3 0.9+0.1 25.3+2.8
  • Nerve growth factor Alzheimer's Disease Diabetic neuropathy Taxol neuropathy Compressive neuropathy AIDS-related neuropathy
  • Brain-derived growth factor Amyotrophic lateral sclerosis
  • Neurotrophin 3 Large fiber neuropathy
  • Insulin-like growth factor Amyotrophic lateral sclerosis Vincristine neuropathy Taxol neuropathy
  • Ciliary neurotrophic factor Amyotrophic lateral sclerosis
  • Glia-derived neurotrophic factor Parkinson's Disease
  • MAP2ab- positive neurons per square centimeter for each region.
  • MAP2 microtubule associated protein a and b
  • TH tyrosine hydroxylase
  • AchE acetylcholine esterase
  • VAT vesicular acetylcholine transporter
  • ChAT choline acetyl transferase
  • GAD glutamic acid decarboxylase
  • NPY neuropeptide Y
  • L-Enk leu-enkephalin
  • M-Enk met- enkephalin.
  • SEPT E15.5 septum
  • LGE E15.5 lateral ganglionic eminence
  • MGE El5.5 medial ganglionic eminence
  • HI E15.5 hippocampus
  • VM E12.5 ventral mesencephalon
  • DM E12.5 dorsal mesencephalon
  • SPC E13.5 spinal cord.

Landscapes

  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biomedical Technology (AREA)
  • Immunology (AREA)
  • Chemical & Material Sciences (AREA)
  • Molecular Biology (AREA)
  • Hematology (AREA)
  • Urology & Nephrology (AREA)
  • Cell Biology (AREA)
  • Biotechnology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Health & Medical Sciences (AREA)
  • Microbiology (AREA)
  • Biochemistry (AREA)
  • Physics & Mathematics (AREA)
  • Medicinal Chemistry (AREA)
  • Analytical Chemistry (AREA)
  • Food Science & Technology (AREA)
  • General Physics & Mathematics (AREA)
  • Pathology (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Toxicology (AREA)
  • Neurology (AREA)
  • Genetics & Genomics (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Organic Chemistry (AREA)
  • Neurosurgery (AREA)
  • General Engineering & Computer Science (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Developmental Biology & Embryology (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)

Abstract

Procédé in vitro selon lequel une population homogène de cellules précurseurs pluripotentes du système nerveux central tirées de neuroépithélium embryonnaire mammalien peuvent être multipliées dans une culture tout en conservant leur capacité de pluripotence. Des conditions chimiquement définies permettent de produire des quantités beaucoup plus élevées de neurones, d'astrocytes ou d'oligodendrocytes. La présente invention concerne également des cultures in vitro de neurones matures à terminaison différenciée et spécifiques d'une région, dérivés de cultures de cellules souches.
PCT/US1998/009236 1997-05-07 1998-05-06 Cellules souches provenant du systeme nerveux central adulte et embryonnaire WO1998050525A1 (fr)

Priority Applications (3)

Application Number Priority Date Filing Date Title
AU72898/98A AU7289898A (en) 1997-05-07 1998-05-06 Embryonic and adult cns stem cells
EP98920291A EP0923640A1 (fr) 1997-05-07 1998-05-06 Cellules souches provenant du systeme nerveux central adulte et embryonnaire
CA002259484A CA2259484A1 (fr) 1997-05-07 1998-05-06 Cellules souches provenant du systeme nerveux central adulte et embryonnaire

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US08/919,580 1997-05-07
US08/919,580 US6040180A (en) 1996-05-23 1997-05-07 In vitro generation of differentiated neurons from cultures of mammalian multipotential CNS stem cells
US5341498A 1998-04-01 1998-04-01
US09/053,414 1998-04-01

Publications (1)

Publication Number Publication Date
WO1998050525A1 true WO1998050525A1 (fr) 1998-11-12

Family

ID=26731841

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US1998/009236 WO1998050525A1 (fr) 1997-05-07 1998-05-06 Cellules souches provenant du systeme nerveux central adulte et embryonnaire

Country Status (4)

Country Link
EP (1) EP0923640A1 (fr)
AU (1) AU7289898A (fr)
CA (1) CA2259484A1 (fr)
WO (1) WO1998050525A1 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013116054A1 (fr) * 2012-02-01 2013-08-08 Albert Einstein College Of Medicine Of Yeshiva University Thérapie par cellules souches neurales pour traiter l'obésité et le diabète

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4775665A (en) * 1983-05-16 1988-10-04 Massachusetts Institute Of Technology Method and composition for treating neurological disorders and aging
US4892538A (en) * 1987-11-17 1990-01-09 Brown University Research Foundation In vivo delivery of neurotransmitters by implanted, encapsulated cells
US5356807A (en) * 1992-09-08 1994-10-18 Cornell Research Foundation Cultured cell line of adult diploid cells from human brain and meningeal tissue
US5411883A (en) * 1989-12-26 1995-05-02 Somatix Therapy Corporation Proliferated neuron progenitor cell product and process
US5753505A (en) * 1995-07-06 1998-05-19 Emory University Neuronal progenitor cells and uses thereof

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4775665A (en) * 1983-05-16 1988-10-04 Massachusetts Institute Of Technology Method and composition for treating neurological disorders and aging
US4892538A (en) * 1987-11-17 1990-01-09 Brown University Research Foundation In vivo delivery of neurotransmitters by implanted, encapsulated cells
US5411883A (en) * 1989-12-26 1995-05-02 Somatix Therapy Corporation Proliferated neuron progenitor cell product and process
US5356807A (en) * 1992-09-08 1994-10-18 Cornell Research Foundation Cultured cell line of adult diploid cells from human brain and meningeal tissue
US5753505A (en) * 1995-07-06 1998-05-19 Emory University Neuronal progenitor cells and uses thereof

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
CATTANEO E., MCKAY R.: "PROLIFERATION AND DIFFERENTIATION OF NEURONAL STEM CELLS REGULATED BY NERVE GROWTH FACTOR.", NATURE, NATURE PUBLISHING GROUP, UNITED KINGDOM, vol. 347., 25 October 1990 (1990-10-25), United Kingdom, pages 762 - 765., XP002914113, ISSN: 0028-0836, DOI: 10.1038/347762a0 *
HUFFAKER T. K., ET AL.: "XENOGRAFTING OF FETAL PIG VENTRAL MESENCEPHALON CORRECTS MOTOR ASYMMETRY IN THE RAT MODEL OF PARKINSON'S DISEASE.", EXPERIMENTAL BRAIN RESEARCH., SPRINGER INTERNATIONAL., DE, vol. 77., 1 January 1989 (1989-01-01), DE, pages 329 - 336., XP002914114, ISSN: 0014-4819, DOI: 10.1007/BF00274990 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013116054A1 (fr) * 2012-02-01 2013-08-08 Albert Einstein College Of Medicine Of Yeshiva University Thérapie par cellules souches neurales pour traiter l'obésité et le diabète

Also Published As

Publication number Publication date
AU7289898A (en) 1998-11-27
EP0923640A1 (fr) 1999-06-23
CA2259484A1 (fr) 1998-11-12

Similar Documents

Publication Publication Date Title
US6040180A (en) In vitro generation of differentiated neurons from cultures of mammalian multipotential CNS stem cells
Vicario‐Abejón et al. Hippocampal stem cells differentiate into excitatory and inhibitory neurons
Barak et al. Human iPSC-derived neural models for studying Alzheimer’s disease: from neural stem cells to cerebral organoids
Johe et al. Single factors direct the differentiation of stem cells from the fetal and adult central nervous system.
Tsai et al. Cell contact regulates fate choice by cortical stem cells
Chambers et al. Spatiotemporal selectivity of response to Notch1 signals in mammalian forebrain precursors
Duval et al. Cell coupling and Cx43 expression in embryonic mouse neural progenitor cells
US7651853B2 (en) Cultures of GFAP+ nestin+ cells that differentiate to neurons
Liu et al. Olfactory bulb core is a rich source of neural progenitor and stem cells in adult rodent and human
Vescovi et al. Establishment and properties of neural stem cell clones: plasticity in vitro and in vivo
Avellana‐Adalid et al. Expansion of rat oligodendrocyte progenitors into proliferative “oligospheres” that retain differentiation potential
Morizane et al. Optimal conditions for in vivo induction of dopaminergic neurons from embryonic stem cells through stromal cell‐derived inducing activity
US20180298333A1 (en) Personalized 3d neural culture system for generating human oligodendrocytes and studying myelination in vitro
Jurga et al. Neurogenic potential of human umbilical cord blood: Neural‐like stem cells depend on previous long‐term culture conditions
Ortega et al. Live imaging of adult neural stem cells in rodents
Uchida et al. Potential functional neural repair with grafted neural stem cells of early embryonic neuroepithelial origin
Niijima et al. Enhanced survival and neuronal differentiation of adrenal chromaffin cells cografted into the striatum with NGF-producing fibroblasts
US12110510B2 (en) Functional cortico-spinal-muscle assembled spheroids
CN101124319B (zh) 神经干细胞
Chen et al. Oligodendrocyte progenitor cells derived from mouse embryonic stem cells give rise to type-1 and type-2 astrocytes in vitro
EP0923640A1 (fr) Cellules souches provenant du systeme nerveux central adulte et embryonnaire
WO1996004368A1 (fr) Propagation et differenciation inductible de cellules souches du systeme nerveux central f×tal humain
Otsu et al. Generation of multipotential NG2 progenitors from mouse embryonic stem cell-derived neural stem cells
Kirner The Generation of Astrocytes from Stem Cells and their Potency to Regain Stem Cell Potential
Kleiderman The Generation of Astrocytes from Stem Cells and Their Potency to Regain Stem Cell Potential

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AU CA JP

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE

ENP Entry into the national phase

Ref document number: 2259484

Country of ref document: CA

Ref country code: CA

Ref document number: 2259484

Kind code of ref document: A

Format of ref document f/p: F

WWE Wipo information: entry into national phase

Ref document number: 1998920291

Country of ref document: EP

121 Ep: the epo has been informed by wipo that ep was designated in this application
WWP Wipo information: published in national office

Ref document number: 1998920291

Country of ref document: EP

WWW Wipo information: withdrawn in national office

Ref document number: 1998920291

Country of ref document: EP

点击 这是indexloc提供的php浏览器服务，不要输入任何密码和下载