Ras family GTPases control growth of astrocyte processes
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作者:
Kalman, D
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Univ Calif San Francisco, Dept Microbiol & Immunol, GW Hooper Fdn Labs, San Francisco, CA 94143 USAUniv Calif San Francisco, Dept Microbiol & Immunol, GW Hooper Fdn Labs, San Francisco, CA 94143 USA
Kalman, D
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Gomperts, SN
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机构:Univ Calif San Francisco, Dept Microbiol & Immunol, GW Hooper Fdn Labs, San Francisco, CA 94143 USA
Gomperts, SN
Hardy, S
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机构:Univ Calif San Francisco, Dept Microbiol & Immunol, GW Hooper Fdn Labs, San Francisco, CA 94143 USA
Hardy, S
Kitamura, M
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机构:Univ Calif San Francisco, Dept Microbiol & Immunol, GW Hooper Fdn Labs, San Francisco, CA 94143 USA
Kitamura, M
Bishop, JM
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机构:Univ Calif San Francisco, Dept Microbiol & Immunol, GW Hooper Fdn Labs, San Francisco, CA 94143 USA
Bishop, JM
机构:
[1] Univ Calif San Francisco, Dept Microbiol & Immunol, GW Hooper Fdn Labs, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Grad Program Neurosci, San Francisco, CA 94143 USA
Astrocytes in neuron-free cultures typically lack processes, although they are highly process-bearing in vivo. We show that basic fibroblast growth factor (bFGF) induces cultured astrocytes to grow processes and that Ras family GTPases mediate these morphological changes. Activated alleles of rac1 and rhoA blocked and reversed bFGF effects when introduced into astrocytes in dissociated culture and in brain slices using recombinant adenoviruses. By contrast, dominant negative (DN) alleles of both GTPases mimicked bFGF effects. A DN allele of Ha-uas blocked bFGF effects but not those of Rac1-DN or RhoA-DN. Our results show that bFGF acting through c-Ha-Ras inhibits endogenous Rad and RhoA GTPases thereby triggering astrocyte process growth, and they provide evidence for the regulation of this cascade in vivo by a yet undetermined neuron-derived factor.