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Astroglial Cells in Development, Regeneration, and RepairChild Study Center, New Haven, CT, Department of Neurobiology, Yale University Medical School, New Haven, CT, flora.vaccarino{at}yale.edu
Child Study Center, New Haven, CT
Child Study Center, New Haven, CT
Child Study Center, New Haven, CT
Department of Pediatrics and Neurology, Yale University Medical School, New Haven, CT
Child Study Center, New Haven, CT
Department of Neurobiology, Yale University Medical School, New Haven, CT
Child Study Center, New Haven, CT
Child Study Center, New Haven, CT Three main cellular components have been described in the CNS: neurons, astrocytes, and oligodendrocytes. In the past 10 years, lineage studies first based on retroviruses in the embryonic CNS and then by genetic fate mapping in both the prenatal and postnatal CNS have proposed that astroglial cells can be progenitors for neurons and oligodendrocytes. Hence, the population of astroglial cells is increasingly recognized as heterogeneous and diverse, encompassing cell types performing widely different roles in development and plasticity. Astroglial cells populating the neurogenic niches increase their proliferation after perinatal injury and in young mice can differentiate into neurons and oligodendrocytes that migrate to the cerebral cortex, replacing the cells that are lost. Although much remains to be learned about this process, it appears that the up-regulation of the Fibroblast growth factor receptor is critical for mediating the injury-induced increase in cell division and perhaps for the neuronal differentiation of astroglial cells. NEUROSCIENTIST 13(2):173185, 2007.
Key Words: Neural stem cells Glial fibrillary acidic protein (GFAP) Radial glia Cerebral cortex Receptor tyrosine kinase Fibroblast growth factor (FGF) Subventricular zone
The Neuroscientist, Vol. 13, No. 2,
173-185 (2007) |
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