Isolation of neural stem cells from the postnatal cerebellum
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Rapoport, M., van Reekum, R. & Mayberg, H. The role of the cerebellum in cognition and behavior: a selective review. J. Neuropsychiatry Clin. Neurosci. 12, 193–198 (2000).
Altman, J. & Bayer, S.A. Development of the Cerebellar System: In Relation to Its Evolution, Structure and Functions (CRC Press, Boca Raton, Florida, USA, 1997).
Kern, J.K. The possible role of the cerebellum in autism/PDD: disruption of a multisensory feedback loop. Med. Hypotheses 59, 255–260 (2002).
Martin, P. & Albers, M. Cerebellum and schizophrenia: a selective review. Schizophr. Bull. 21, 241–250 (1995).
Wechsler-Reya, R. & Scott, M.P. The developmental biology of brain tumors. Annu. Rev. Neurosci. 24, 385–428 (2001).
Wetmore, C. Sonic hedgehog in normal and neoplastic proliferation: insight gained from human tumors and animal models. Curr. Opin. Genet. Dev. 13, 34–42 (2003).
Zhang, L. & Goldman, J.E. Generation of cerebellar interneurons from dividing progenitors in white matter. Neuron 16, 47–54 (1996).
Hallonet, M.E., Teillet, M.A. & Le Douarin, N.M. A new approach to the development of the cerebellum provided by the quail-chick marker system. Development 108, 19–31 (1990).
Lumpkin, E.A. et al. Math1-driven GFP expression in the developing nervous system of transgenic mice. Gene Expr. Patterns 3, 389–395 (2003).
Wechsler-Reya, R.J. & Scott, M.P. Control of neuronal precursor proliferation in the cerebellum by Sonic Hedgehog. Neuron 22, 103–114 (1999).
Cheng, Y., Tao, Y., Black, I.B. & DiCicco-Bloom, E. A single peripheral injection of basic fibroblast growth factor (bFGF) stimulates granule cell production and increases cerebellar growth in newborn rats. J. Neurobiol. 46, 220–229 (2001).
Wernecke, H., Lindner, J. & Schachner, M. Cell type specificity and developmental expression of the L2/HNK-1 epitopes in mouse cerebellum. J. Neuroimmunol. 9, 115–130 (1985).
Theodosis, D.T., Rougon, G. & Poulain, D.A. Retention of embryonic features by an adult neuronal system capable of plasticity: polysialylated neural cell adhesion molecule in the hypothalamo-neurohypophysial system. Proc. Natl. Acad. Sci. USA 88, 5494–5498 (1991).
Tucker, R.P., Binder, L.I., Viereck, C., Hemmings, B.A. & Matus, A.I. The sequential appearance of low- and high-molecular-weight forms of MAP2 in the developing cerebellum. J. Neurosci. 8, 4503–4512 (1988).
Sommer, I. & Schachner, M. Monoclonal antibodies (O1 to O4) to oligodendrocyte surfaces: an immunocytological study in the central nervous system. Dev. Biol. 83, 311–327 (1981).
Dawson, M.R., Polito, A., Levine, J.M. & Reynolds, R. NG2-expressing glial progenitor cells: an abundant and widespread population of cycling cells in the adult rat CNS. Mol. Cell. Neurosci. 24, 476–488 (2003).
Bignami, A., Eng, L.F., Dahl, D. & Uyeda, C.T. Localization of the glial fibrillary acidic protein in astrocytes by immunofluorescence. Brain Res. 43, 429–435 (1972).
Geisert, E.E., Jr., Yang, L. & Irwin, M.H. Astrocyte growth, reactivity, and the target of the antiproliferative antibody, TAPA. J. Neurosci. 16, 5478–5487 (1996).
Haegel, H., Tolg, C., Hofmann, M. & Ceredig, R. Activated mouse astrocytes and T cells express similar CD44 variants. Role of CD44 in astrocyte/T cell binding. J. Cell Biol. 122, 1067–1077 (1993).
Lendahl, U., Zimmerman, L.B. & McKay, R.D. CNS stem cells express a new class of intermediate filament protein. Cell 60, 585–595 (1990).
Corbeil, D., Roper, K., Fargeas, C.A., Joester, A. & Huttner, W.B. Prominin: a story of cholesterol, plasma membrane protrusions and human pathology. Traffic 2, 82–91 (2001).
Graham, V., Khudyakov, J., Ellis, P. & Pevny, L. SOX2 functions to maintain neural progenitor identity. Neuron 39, 749–765 (2003).
Sakakibara, S. et al. Mouse-Musashi-1, a neural RNA-binding protein highly enriched in the mammalian CNS stem cell. Dev. Biol. 176, 230–242 (1996).
Sawamoto, K. et al. Generation of dopaminergic neurons in the adult brain from mesencephalic precursor cells labeled with a nestin-GFP transgene. J. Neurosci. 21, 3895–3903 (2001).
Tamaki, S. et al. Engraftment of sorted/expanded human central nervous system stem cells from fetal brain. J. Neurosci. Res. 69, 976–986 (2002).
Reynolds, B.A. & Weiss, S. Generation of neurons and astrocytes from isolated cells of the adult mammalian central nervous system. Science 255, 1707–1710 (1992).
Imura, T., Kornblum, H.I. & Sofroniew, M.V. The predominant neural stem cell isolated from postnatal and adult forebrain but not early embryonic forebrain expresses GFAP. J. Neurosci. 23, 2824–2832 (2003).
Takahashi, J., Palmer, T.D. & Gage, F.H. Retinoic acid and neurotrophins collaborate to regulate neurogenesis in adult-derived neural stem cell cultures. J. Neurobiol. 38, 65–81 (1999).
Galli, R., Pagano, S.F., Gritti, A. & Vescovi, A.L. Regulation of neuronal differentiation in human CNS stem cell progeny by leukemia inhibitory factor. Dev. Neurosci. 22, 86–95 (2000).
Erlandsson, A., Enarsson, M. & Forsberg-Nilsson, K. Immature neurons from CNS stem cells proliferate in response to platelet-derived growth factor. J. Neurosci. 21, 3483–3491 (2001).
Aoki, E., Semba, R. & Kashiwamata, S. New candidates for GABAergic neurons in the rat cerebellum: an immunocytochemical study with anti-GABA antibody. Neurosci. Lett. 68, 267–271 (1986).
Simmons, M.L. & Dutton, G.R. Neuronal origins of K+-evoked amino acid release from cerebellar cultures. J. Neurosci. Res. 31, 646–653 (1992).
Maricich, S.M. & Herrup, K. Pax-2 expression defines a subset of GABAergic interneurons and their precursors in the developing murine cerebellum. J. Neurobiol. 41, 281–294 (1999).
Aruga, J. et al. A novel zinc finger protein, zic, is involved in neurogenesis, especially in the cell lineage of cerebellar granule cells. J. Neurochem. 63, 1880–1890 (1994).
Shetty, A.K. & Turner, D.A. In vitro survival and differentiation of neurons derived from epidermal growth factor-responsive postnatal hippocampal stem cells: inducing effects of brain-derived neurotrophic factor. J. Neurobiol. 35, 395–425 (1998).
Laywell, E.D., Rakic, P., Kukekov, V.G., Holland, E.C. & Steindler, D.A. Identification of a multipotent astrocytic stem cell in the immature and adult mouse brain. Proc. Natl. Acad. Sci. USA 97, 13883–13888 (2000).
Singh, S.K. et al. Identification of a cancer stem cell in human brain tumors. Cancer Res. 63, 5821–5828 (2003).
Gabay, L., Lowell, S., Rubin, L.L. & Anderson, D.J. Deregulation of dorsoventral patterning by FGF confers trilineage differentiation capacity on CNS stem cells in vitro. Neuron 40, 485–499 (2003).
Gao, W.Q. & Hatten, M.E. Immortalizing oncogenes subvert the establishment of granule cell identity in developing cerebellum. Development 120, 1059–1070 (1994).
Snyder, E.Y. et al. Multipotent neural cell lines can engraft and participate in development of mouse cerebellum. Cell 68, 33–51 (1992).
Milosevic, A. & Goldman, J.E. Progenitors in the postnatal cerebellar white matter are antigenically heterogeneous. J. Comp. Neurol. 452, 192–203 (2002).
Alder, J., Cho, N.K. & Hatten, M.E. Embryonic precursor cells from the rhombic lip are specified to a cerebellar granule neuron identity. Neuron 17, 389–399 (1996).
Zinyk, D.L., Mercer, E.H., Harris, E., Anderson, D.J. & Joyner, A.L. Fate mapping of the mouse midbrain-hindbrain constriction using a site-specific recombination system. Curr. Biol. 8, 665–668 (1998).
Pietsch, T. et al. Medulloblastomas of the desmoplastic variant carry mutations of the human homologue of Drosophila patched. Cancer Res. 57, 2085–2088 (1997).
Pomeroy, S.L. et al. Prediction of central nervous system embryonal tumour outcome based on gene expression. Nature 415, 436–442 (2002).
Katsetos, C.D. et al. Calbindin-D28k in subsets of medulloblastomas and in the human medulloblastoma cell line D283 Med. Arch. Pathol. Lab. Med. 119, 734–743 (1995).
Hemmati, H.D. et al. Cancerous stem cells can arise from pediatric brain tumors. Proc. Natl. Acad. Sci. USA 100, 15178–15183 (2003).
Weigmann, A., Corbeil, D., Hellwig, A. & Huttner, W.B. Prominin, a novel microvilli-specific polytopic membrane protein of the apical surface of epithelial cells, is targeted to plasmalemmal protrusions of non-epithelial cells. Proc. Natl. Acad. Sci. USA 94, 12425–12430 (1997).