Cell Contact Regulates Fate Choice by Cortical Stem Cells

Cell fate is determined by intrinsic programs and external cues, such as soluble signals and cell–cell contact. Previous studies have demonstrated the roles of soluble factors in the proliferation and differentiation of cortical stem cells and cell–cell contact in maintaining stem cells in a proliferative state. In the present study, we focused on the effect of cell–cell interaction on cell-fate determination. We found that density could exert a strong influence on the cell-type composition when cortical stem cells differentiate. Multipotent stem cells, which normally gave rise to neurons, astrocytes, and oligodendrocytes under high-density culture condition, differentiated almost exclusively into smooth muscle at low density. Clonal analysis indicated that smooth muscle and astrocytes were derived from a common precursor and that the density effect on cell types used an instructive mechanism on the choice of fate rather than an effect of selective survival and/or proliferation. This instructive mechanism depended on the local and not the average density of the cells. This local signal could be mimicked by membrane extract. These findings demonstrate the importance of membrane-bound signals in specifying lineage and provide the first evidence for a short-range regulatory mechanism in cortical stem cell differentiation.

[1]  T. Ben-Hur,et al.  Polysialylated Neural Cell Adhesion Molecule-Positive CNS Precursors Generate Both Oligodendrocytes and Schwann Cells to Remyelinate the CNS after Transplantation , 1999, The Journal of Neuroscience.

[2]  R. McKay,et al.  Single factors direct the differentiation of stem cells from the fetal and adult central nervous system. , 1996, Genes & development.

[3]  S. Weiss,et al.  Generation of neurons and astrocytes from isolated cells of the adult mammalian central nervous system. , 1992, Science.

[4]  S. Masur,et al.  TGF-beta receptor expression and smad2 localization are cell density dependent in fibroblasts. , 2000, Investigative ophthalmology & visual science.

[5]  M. Raff,et al.  Differentiation signals in the CNS: Type-2 astrocyte development in vitro as a model system , 1990, Neuron.

[6]  R. Alon,et al.  Dependence of human stem cell engraftment and repopulation of NOD/SCID mice on CXCR4. , 1999, Science.

[7]  Sara Jacob,et al.  Mammalian NUMB is an evolutionarily conserved signaling adapter protein that specifies cell fate , 1996, Current Biology.

[8]  S. Minoguchi,et al.  Involvement of RBP-J in biological functions of mouse Notch1 and its derivatives. , 1997, Development.

[9]  C. Cepko,et al.  Widespread dispersion of neuronal clones across functional regions of the cerebral cortex. , 1992, Science.

[10]  E. Olson,et al.  SM22 alpha, a marker of adult smooth muscle, is expressed in multiple myogenic lineages during embryogenesis. , 1996, Circulation research.

[11]  R. Gebhardt,et al.  Common myofibroblastic features of newborn rat astrocytes and cirrhotic rat liver stellate cells in early cultures and in vivo , 1999, Neurochemistry International.

[12]  R. McKay,et al.  CNS stem cells express a new class of intermediate filament protein , 1990, Cell.

[13]  J. Price,et al.  The generation of neurons and oligodendrocytes from a common precursor cell , 1991, Neuron.

[14]  J. Sanes,et al.  Use of a recombinant retrovirus to study post‐implantation cell lineage in mouse embryos. , 1986, The EMBO journal.

[15]  F. Gage,et al.  Stem cells of the central nervous system. , 1998, Current opinion in neurobiology.

[16]  G. Owens,et al.  Regulation of differentiation of vascular smooth muscle cells. , 1995, Physiological reviews.

[17]  V. Caviness,et al.  The cell cycle of the pseudostratified ventricular epithelium of the embryonic murine cerebral wall , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[18]  M. Rao,et al.  A common neural progenitor for the CNS and PNS. , 1998, Developmental biology.

[19]  C. Cepko,et al.  Lineage analysis in the vertebrate nervous system by retrovirus-mediated gene transfer. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[20]  S. Weiss,et al.  A multipotent EGF-responsive striatal embryonic progenitor cell produces neurons and astrocytes , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[21]  F. Pfrieger,et al.  Synaptic efficacy enhanced by glial cells in vitro. , 1997, Science.

[22]  G. Gabbiani,et al.  Smooth muscle alpha-actin is a marker for hair follicle dermis in vivo and in vitro. , 1991, Journal of cell science.

[23]  E. Olson,et al.  Expression of the Smooth Muscle Cell Calponin Gene Marks the Early Cardiac and Smooth Muscle Cell Lineages during Mouse Embryogenesis (*) , 1996, The Journal of Biological Chemistry.

[24]  F. Mcmorris,et al.  Insulin‐like growth factor I promotes cell proliferation and oligodendroglial commitment in rat glial progenitor cells developing in vitro , 1988, Journal of neuroscience research.

[25]  N. L. Hayes,et al.  Local Homogeneity of Cell Cycle Length in Developing Mouse Cortex , 1997, The Journal of Neuroscience.

[26]  B. Pessac,et al.  α Isoform of smooth muscle actin is expressed in astrocytes in vitro and in vivo , 1991 .

[27]  Raphael Kopan,et al.  An activated Notch suppresses neurogenesis and myogenesis but not gliogenesis in mammalian cells. , 1994, Development.

[28]  Y. Jan,et al.  Differential expression of mammalian Numb, Numblike and Notch1 suggests distinct roles during mouse cortical neurogenesis. , 1997, Development.

[29]  E. Morrisey,et al.  Structure and Expression of a Smooth Muscle Cell-specific Gene, SM22α (*) , 1995, The Journal of Biological Chemistry.

[30]  J. Sanes,et al.  Neurons and glia arise from a common progenitor in chicken optic tectum: demonstration with two retroviruses and cell type-specific antibodies. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[31]  E. Morrisey,et al.  Structure and expression of a smooth muscle cell-specific gene, SM22 alpha. , 1995, The Journal of biological chemistry.

[32]  L. Richards,et al.  Leukaemia Inhibitory Factor or Related Factors Promote the Differentiation of Neuronal and Astrocytic Precursors within the Developing Murine Spinal Cord , 1996, The European journal of neuroscience.

[33]  K. Hiwada,et al.  cDNA cloning and mRNA expression of calponin and SM22 in rat aorta smooth muscle cells. , 1993, Gene.

[34]  Kenji Matsuno,et al.  Notch signaling. , 1995, Science.

[35]  M. Hatten,et al.  Neuronal regulation of astroglial morphology and proliferation in vitro , 1985, The Journal of cell biology.

[36]  J. Sanes,et al.  Cell lineage in the cerebral cortex of the mouse studied in vivo and in vitro with a Recombinant Retrovirus , 1988, Neuron.

[37]  Y. Jan,et al.  Asymmetric Localization of a Mammalian Numb Homolog during Mouse Cortical Neurogenesis , 1996, Neuron.

[38]  P. Scambler,et al.  HIRA, a mammalian homologue of Saccharomyces cerevisiae transcriptional co-repressors, interacts with Pax3 , 1998, Nature Genetics.

[39]  A. Represa,et al.  Acidic Calponin Cloned from Neural Cells is Differentially Expressed During Rat Brain Development , 1996, The European journal of neuroscience.

[40]  Y. Ben-Ari,et al.  Expression of an acidic isoform of calponin in rat brain: western blots on one- or two-dimensional gels and immunolocalization in cultured cells. , 1995, The Biochemical journal.

[41]  C. Ware,et al.  Neural precursor differentiation into astrocytes requires signaling through the leukemia inhibitory factor receptor. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[42]  M. Greenberg,et al.  Distinct roles for bFGF and NT-3 in the regulation of cortical neurogenesis , 1995, Neuron.

[43]  S. Artavanis-Tsakonas,et al.  Human deltex is a conserved regulator of Notch signalling , 1998, Nature Genetics.

[44]  Y. Ben-Ari,et al.  Distribution of caldesmon and of the acidic isoform of calponin in cultured cerebellar neurons and in different regions of the rat brain: an immunofluorescence and confocal microscopy study. , 1995, Experimental cell research.

[45]  M. Hatten Neuronal inhibition of astroglial cell proliferation is membrane mediated , 1987, The Journal of cell biology.

[46]  G H Sato,et al.  Growth of a rat neuroblastoma cell line in serum-free supplemented medium. , 1979, Proceedings of the National Academy of Sciences of the United States of America.

[47]  M. Bronner‐Fraser,et al.  Neural crest induction in Xenopus: evidence for a two-signal model. , 1998, Development.

[48]  F. Gage,et al.  Isolation, characterization, and use of stem cells from the CNS. , 1995, Annual review of neuroscience.

[49]  S. Temple Division and differentiation of isolated CNS blast cells in microculture , 1989, Nature.

[50]  A. Frankfurter,et al.  The expression and posttranslational modification of a neuron-specific beta-tubulin isotype during chick embryogenesis. , 1990, Cell motility and the cytoskeleton.

[51]  Raphael Kopan,et al.  Notch on the cutting edge. , 1997, Trends in genetics : TIG.

[52]  G. Gabbiani,et al.  Appearance of alpha-smooth muscle actin in human eye lens cells of anterior capsular cataract and in cultured bovine lens-forming cells. , 1990, Differentiation; research in biological diversity.

[53]  M. Hatten,et al.  Cerebellar granule cell neurogenesis is regulated by cell-cell interactions in vitro , 1991, Neuron.

[54]  S. Temple,et al.  Isolated rat cortical progenitor cells are maintained in division in vitro by membrane-associated factors. , 1994, Development.

[55]  T. Kilpatrick,et al.  Cloning and growth of multipotential neural precursors: Requirements for proliferation and differentiation , 1993, Neuron.