Oligodendrocytes derived from human embryonic stem cells for...

Chemistry: molecular biology and microbiology – Animal cell – per se ; composition thereof; process of... – Method of regulating cell metabolism or physiology

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C435S007210, C424S093700

Reexamination Certificate

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10406817

ABSTRACT:
This invention provides populations of neural cells bearing markers of glial cells, such as oligodendrocytes and their precursors. The populations are generated by differentiating pluripotent stem cells such as human embryonic stem cells under conditions that promote enrichment of cells with the desired phenotype or functional capability. Various combinations of differentiation factors and mitogens can be used to produce cell populations that are over 95% homogeneous in morphological appearance, and the expression of oligodendrocyte markers such as GalC. The cells are capable of forming myelin sheaths, and can be used therapeutically improve function of the central nervous system.

REFERENCES:
patent: 5654183 (1997-08-01), Anderson et al.
patent: 5750376 (1998-05-01), Weiss et al.
patent: 5753506 (1998-05-01), Johe
patent: 5766948 (1998-06-01), Gage et al.
patent: 5830621 (1998-11-01), Suzuki et al.
patent: 5830651 (1998-11-01), Cauley et al.
patent: 5849553 (1998-12-01), Anderson et al.
patent: 5851832 (1998-12-01), Weiss et al.
patent: 5928947 (1999-07-01), Anderson et al.
patent: 5968829 (1999-10-01), Carpenter
patent: 6040180 (2000-03-01), Johe
patent: 6090622 (2000-07-01), Gearhart et al.
patent: 6200806 (2001-03-01), Thomson
patent: 6235537 (2001-05-01), North et al.
patent: 6238922 (2001-05-01), Uchida
patent: 6245564 (2001-06-01), Goldman et al.
patent: 6887706 (2005-05-01), Zhang et al.
patent: 2002/0019046 (2002-02-01), Carpenter
patent: 2253078 (1998-10-01), None
patent: WO 97/07200 (1997-02-01), None
patent: WO 97/32608 (1997-02-01), None
patent: WO 98/50526 (1998-11-01), None
patent: WO 99/01159 (1999-01-01), None
patent: WO 99/20741 (1999-04-01), None
patent: WO 00/23571 (2000-04-01), None
patent: WO 01/28342 (2001-04-01), None
patent: WO 01/51610 (2001-07-01), None
patent: WO 01/68815 (2001-09-01), None
patent: WO 01/88104 (2001-11-01), None
patent: WO 01/98463 (2001-12-01), None
Wohl 1998. J. Neurobiol 37:281-290.
Nishiyama 1996. Journal of Neuroscience Research 43:299-314.
Guan, et al. “Embryonic stem cell-derived neurogenesis. Retinoic acid induction and lineage selection of neuronal cells”,Cell Tissue Res.,(2001) vol. 305(2): 171-176.
Hinks, et al. “Depletion of endogenous oligodendrocyte progenitors rather than increased availability of survival factors is a likely explanation for enhanced survival of transplanted oligodendrocyte progenitors in X-irradiated compared to normal CNS”,Neuropath. Appl. Neurobio.,(2001) vol. 27: 59-67.
Holland. “Gliomagenesis: Genetic alterations and mouse models”,Nat. Rev. Genet.,(2001) vol. 2(2): 120-129.
Keirstead, et al. “In vivo immunological suppression of spinal cord myelin development”,Brain Res. Bulletin,(1997) vol. 44(6): 727-734.
Keirstead, et al. “Identification of post-mitotic oligodenderocytes incapable of remyelination within the demyelinated adult spinal cord”,J. Neuropath. Exp. Neurology,(1997) vol. 56(11): 1191-1201.
Keirstead, et al. “A quantifiable model of axonal regeneration in the demyelinated adult rat spinal cord”,Exp. Neurol.,(1998) vol. 151: 303-313.
Keirstead, et al. “Response of the oligodendrocyte progenitor cell population (defined by NG2 labelling) to demyelination of the adult spinal cord”,GLIA,(1998) vol. 22: 161-170.
Keirstead, et al. “The role of oligodendrocytes and oligodendrocyte progenitors in CNS remyelination”,Adv. Exp. Med. Biol.,(1999) vol. 468: 183-197.
Keirstead, et al. “Polysialylated neural cell adhesion molecule-positive CNS precursors generate both oligodendrocytes and schwann cells to remyelinate the CNS after transplantation”,J. Neurosci.,(1999) vol. 19(17): 7529-7536.
Keirstead. “Stem cell transplantation into the central nervous system and the control of differentiation”,J. Neurosci. Res.,(2001) vol. 63: 233-236.
Kornblum, et al. “Molecular markers in CNS stem cell research: Hitting a moving target”,Nature Reviews,(2001) vol. 2: 843-846.
Lee, et al. “Efficient generation of midbrain and hindbrain neurons from mouse embryonic stem cells”,Nature Biotech.,(2000) vol. 18: 675-678.
Li, et al. “Generation of purified neural precursors from embryonic stem cells by lineage selection”,Curr. Bio.,(1998) vol. 8: 971-974.
Liu, et al. “Embryonic stem cells differentiate into oligodendrocytes and myelinate in culture and after spinal cord transplantation”,Proc. Natl. Acad. Sci. USA,(2000) vol. 97(11): 6126-6131.
McDonald, et al. “Transplanted embryonic stem cells survive, differentiate and promote recovery in injured rat spinal cord”,Nature Med.,(1999) vol. 5(12): 1410-1412.
Mujtaba, et al. “Lineage-restricted neural precursors can be isolated from both the mouse neural tube and cultured ES cells”,Dev. Bio.,(1999) vol. 214: 113-127.
O'Shea. “Neuronal differentiation of mouse embryonic stem cells: Lineage selection and forced differentiation paradigms”,Blood Cells, Molecules and Diseases,(2001) vol. 27(3): 705-712.
Ostenfeld, et al. “Regional specification of rodent and human neurospheres”,Brain Res. Dev. Brain Res.,(2002) vol. 134(1-2): 43-55.
Pardo, et al. “Differentiation of rat striatal embryonic stem cells in vitro: Monolayer culture vs. three-dimensional coculture with differentiated brain cells”,J. Neurosci. Res,(2000) vol. 59(4): 504-512.
Park, et al. “Transplantation of neural progenitor and stem cells: Developmental insights may suggest new therapies for spinal cord and other CNS dysfunction”,J. Neurotrauma,(1999) vol. 16(8):675-687.
Reubinoff, et al. “Neural progenitors from human embryonic stem cells”,Nat. Biotechnol.,(2001) vol. 19(12): 1134-1140.
Scolding, et al. “Oligodendrocyte progenitors are present in the normal adult human CNS and in the lesions of multiple sclerosis”,Brain,(1998) vol. 121: 2221-2228.
Scolding, et al. “Identification of A2B5-positive putative oligodendrocyte progenitor cells and A2B5-positive astrocytes in adult human white matter”,Neuroscience,(1999) vol. 89(1): 1-4.
Svendsen, et al. “A new method for the rapid and long term growth of human neural precursor cells”,J. Neurosci. Meth.,(1998) vol. 85: 141-152.
Thomson, et al. “Neural differentiation of rhesus embryonic stem cells”,APMIS,(1998) vol. 106: 149-157.
Thomson, et al. “Embryonic Stem Cell Lines Derived From Human Blastocysts”Science,(1998) vol. 282 (5391):1145.
Xu, et al. “Feeder-free growth of undifferentiated human embryonic stem cells”,Biotechnol.,(2001) vol. 19: 971-974.
Zhang, et al. “In vitro differentiation of transplantable neural precursors from human embryonic stem cells”,Nature Biotech.,(2001) vol. 19: 1129-1133.
Kalman, et al. “Spectrum and classification of inflammatory demyelinating diseases of the central nervous system”,Curr. Neurology and Neurosci. Reports,(2001) vol. 1: 249-256.
Keirstead, et al. “Enhanced axonal regeneration following combined demyelination plus schwann cell transplantation therapy in the injured adult spinal cord”,Exp. Neurol.,(1999) vol. 159(1): 225-236.
Kuo, et al. “Differentiation of monkey embryonic stem cells into neural lineages”,Biol. Reprod.,(2002).
Lie, et al. “The adult substantia nigra contains progenitor cells with neurogenic potential”,J. Neurosci.(2002) vol. 22(15): 6639-6649.
McDonald, et al. “Repairing the damaged spinal cord”,Scientific American,(1999) vol. 281(3): 64-73.
Xian, et al. “A subset of ES-cell-derived neural cells marked by gene targeting”,Stem Cells,(2003) vol. 21: 41-49.
Zhang, et al. “Adult brain retains the potential to generate oligodendroglial progenitors with extensive myelination capacity”,Proc. Natl. Acad. Sci. USA,(1999) vol. 96: 4089-4094.
Blakemore W.F. et al., “The Origin of Remyelinating Cells in The Central Nervous System.”

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