An antagonistic interaction between PlexinB2 and Rnd3 controls RhoA activity and cortical neuron migration

被引:52
作者
Azzarelli, Roberta [1 ]
Pacary, Emilie [1 ]
Garg, Ritu [2 ]
Garcez, Patricia [1 ]
van den Berg, Debbie [1 ]
Riou, Philippe [2 ]
Ridley, Anne J. [2 ]
Friedel, Roland H. [3 ]
Parsons, Maddy [2 ]
Guillemot, Francois [1 ]
机构
[1] Natl Inst Med Res, MRC, Div Mol Neurobiol, London NW7 1AA, England
[2] Kings Coll London, Randall Div Cell & Mol Biophys, London SE1 1UL, England
[3] Icahn Sch Med Mt Sinai, Dept Neurosci, New York, NY 10029 USA
基金
英国医学研究理事会; 英国惠康基金; 英国生物技术与生命科学研究理事会;
关键词
NUCLEOTIDE EXCHANGE FACTORS; GTPASE-ACTIVATING PROTEIN; DEVELOPING MOUSE-BRAIN; RADIAL MIGRATION; SEMAPHORIN RECEPTORS; CEREBRAL-CORTEX; NERVOUS-SYSTEM; PDZ-RHOGEF; RAS-GTPASE; R-RAS;
D O I
10.1038/ncomms4405
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
A transcriptional programme initiated by the proneural factors Neurog2 and Ascl1 controls successive steps of neurogenesis in the embryonic cerebral cortex. Previous work has shown that proneural factors also confer a migratory behaviour to cortical neurons by inducing the expression of the small GTP-binding proteins such as Rnd2 and Rnd3. However, the directionality of radial migration suggests that migrating neurons also respond to extracellular signal-regulated pathways. Here we show that the Plexin B2 receptor interacts physically and functionally with Rnd3 and stimulates RhoA activity in migrating cortical neurons. Plexin B2 competes with p190RhoGAP for binding to Rnd3, thus blocking the Rnd3-mediated inhibition of RhoA and also recruits RhoGEFs to directly stimulate RhoA activity. Thus, an interaction between the cell-extrinsic Plexin signalling pathway and the cell-intrinsic Ascl1-Rnd3 pathway determines the level of RhoA activity appropriate for cortical neuron migration.
引用
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页数:12
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