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. 1994 Nov;127(3):813-23.
doi: 10.1083/jcb.127.3.813.

Reexpression of glial fibrillary acidic protein rescues the ability of astrocytoma cells to form processes in response to neurons

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Reexpression of glial fibrillary acidic protein rescues the ability of astrocytoma cells to form processes in response to neurons

W J Chen et al. J Cell Biol. 1994 Nov.

Abstract

Astroglial cells play an important role in orchestrating the migration and positioning of neurons during central nervous system development. Primary astroglia, as well as astrocytoma cells will extend long stable processes when co-cultured with granule neurons. In order to determine the function of the glial fibrillary acidic protein (GFAP), the major intermediate filament protein in astroglia and astrocytoma cells, we suppressed the expression of GFAP by stable transfection of an anti-sense GFAP construct in human astrocytoma U251MG cells. The resulting AS2-U251 cells can no longer extend stable processes in the presence of granule neurons. To show that this effect is due specifically to the absence of GFAP, we reintroduced a fully encoding rat brain GFAP cDNA into these AS2-U251 cells. The resulting rat GFAP appeared as a filamentous network and the reexpression of GFAP rescued the ability of these astrocytoma cells to form stable processes when co-cultured with neurons. From these results, it is clear that the glial specific intermediate filament protein, GFAP, is required for process extension of these astrocytoma cells in response to granule neurons.

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References

    1. J Comp Neurol. 1973 Nov 15;152(2):103-32 - PubMed
    1. Brain Res. 1973 Nov 9;62(1):1-35 - PubMed
    1. Int J Cancer. 1973 Sep 15;12(2):438-51 - PubMed
    1. Nature. 1974 Jul 5;250(461):31-4 - PubMed
    1. J Cell Biol. 1987 Nov;105(5):2307-14 - PubMed

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