Literature DB >> 2215915

Organization of radial glia and related cells in the developing murine CNS. An analysis based upon a new monoclonal antibody marker.

M A Edwards1, M Yamamoto, V S Caviness.   

Abstract

A monoclonal antibody, RC1, has been generated which provides a selective and sensitive immunohistochemical marker of radial glial cells and related cell forms during development of the mouse CNS. Beginning on embryonic day E10, immunocytochemistry performed on cryostat sections stains throughout the CNS a subpopulation of cells in the ventricular zone with radial processes that terminate with endfeet at the pial surface. These processes become fasciculated and attain maximal densities by E12-14 in the spinal cord and lower brainstem and by E14-16 in the midbrain, cerebellum and forebrain. Fasciculation is especially prominent for a subclass of these cells at the midline of the brainstem and spinal cord. As nuclear and cortical structures develop, the trajectories of the radial fiber fascicles undergo systematic and region-specific distortions in their initially simple linear configuration, in the process maintaining a consistent spatial registration of germinal ventricular zones with distal sites of assembly of post-migratory neurons. In the late fetal period, radial glial progressively disappear and scattered immature astrocytes bearing multiple fine processes appear in most regions of the CNS. In the spinal cord, a transitional unipolar radial form is identified in the emerging ventral and lateral funiculi between E13 and E17. In the cerebellum, precursors to the unipolar Bergmann glial cell are identified by E15, and in the retina, precursors of the bipolar Müller cell are identified by E16. Postnatally, RC1-stained radial glia become sparse, and after one week, immunoreactive cells include only ependymal cells, hypothalamic tanycytes, Bergmann glia, Müller cells, a unipolar radial form in the dentate gyrus, and a subpopulation of white matter astrocytes. These results suggest that radial cells of astroglial lineage comprise a diverse set of cell classes which subserve multiple functions in the developing and adult brain.

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Year:  1990        PMID: 2215915     DOI: 10.1016/0306-4522(90)90356-9

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  34 in total

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Review 2.  Don't fence me in: harnessing the beneficial roles of astrocytes for spinal cord repair.

Authors:  Robin E White; Lyn B Jakeman
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Review 3.  Bergmann glia function in granule cell migration during cerebellum development.

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Journal:  Mol Neurobiol       Date:  2013-01-19       Impact factor: 5.590

Review 4.  Radial glia, the keystone of the development of the hippocampal dentate gyrus.

Authors:  Le Xu; Xiaotong Tang; Ying Wang; Haiwei Xu; Xiaotang Fan
Journal:  Mol Neurobiol       Date:  2014-04-10       Impact factor: 5.590

5.  Early postnatal astroglial cells produce multilineage precursors and neural stem cells in vivo.

Authors:  Yosif M Ganat; John Silbereis; Clinton Cave; Hai Ngu; George M Anderson; Yasushi Ohkubo; Laura R Ment; Flora M Vaccarino
Journal:  J Neurosci       Date:  2006-08-16       Impact factor: 6.167

6.  Dynamics of cell migration from the lateral ganglionic eminence in the rat.

Authors:  J A de Carlos; L López-Mascaraque; F Valverde
Journal:  J Neurosci       Date:  1996-10-01       Impact factor: 6.167

Review 7.  The involvement of astrocytes and kynurenine pathway in Alzheimer's disease.

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8.  Bergmann glial development in the mouse cerebellum as revealed by tenascin expression.

Authors:  S Yuasa
Journal:  Anat Embryol (Berl)       Date:  1996-09

9.  Neurotropism of mouse-adapted haemagglutinating encephalomyelitis virus.

Authors:  K Yagami; Y Izumi; N Kajiwara; F Sugiyama; Y Sugiyama
Journal:  J Comp Pathol       Date:  1993-07       Impact factor: 1.311

10.  Defects of neuronal migration and the pathogenesis of cortical malformations are associated with Small eye (Sey) in the mouse, a point mutation at the Pax-6-locus.

Authors:  W Schmahl; M Knoedlseder; J Favor; D Davidson
Journal:  Acta Neuropathol       Date:  1993       Impact factor: 17.088

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