Essential and distinct roles for cdc42 and rac1 in the regulation of Schwann cell biology during peripheral nervous system development

被引:160
作者
Benninger, Yves
Thurnherr, Tina
Pereira, Jorge A.
Krause, Sven
Wu, Xunwei
Chrostek-Grashoff, Anna
Herzog, Dominik
Nave, Klaus-Armin
Franklin, Robin J. M.
Meijer, Dies
Brakebusch, Cord
Suter, Ueli
Relvas, Joao B. [1 ]
机构
[1] ETH, Dept Biol, Inst Cell Biol, CH-8093 Zurich, Switzerland
[2] Univ Copenhagen, Dept Mol Pathol, DK-2100 Copenhagen, Denmark
[3] Max Planck Inst Expt Med, Dept Neurogenet, D-82152 Martinsried, Germany
[4] Univ Cambridge, Dept Vet Med, Cambridge Ctr Brain Repair, Cambridge CB3 0ES, England
[5] Univ Cambridge, Dept Vet Med, Dept Neuroregenerat LAb, Cambridge CB3 0ES, England
[6] Erasmus Univ, Med Ctr, Dept Cell Biol & Genet, NL-3000 DR Rotterdam, Netherlands
关键词
D O I
10.1083/jcb.200610108
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
During peripheral nervous system ( PNS) myelination, Schwann cells must interpret extracellular cues to sense their environment and regulate their intrinsic developmental program accordingly. The pathways and mechanisms involved in this process are only partially understood. We use tissue-specific conditional gene targeting to show that members of the Rho GTPases, cdc42 and rac1, have different and essential roles in axon sorting by Schwann cells. Our results indicate that although cdc42 is required for normal Schwann cell proliferation, rac1 regulates Schwann cell process extension and stabilization, allowing efficient radial sorting of axon bundles.
引用
收藏
页码:1051 / 1061
页数:11
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