Plexin-B1 directly interacts with PDZ-RhoGEF/LARG to regulate RhoA and growth cone morphology

被引:308
作者
Swiercz, JM
Kuner, R
Behrens, J
Offermanns, S
机构
[1] Heidelberg Univ, Inst Pharmacol, D-69120 Heidelberg, Germany
[2] Univ Erlangen Nurnberg, Nikolaus Fiebiger Ctr, D-91054 Erlangen, Germany
关键词
D O I
10.1016/S0896-6273(02)00750-X
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Plexins are widely expressed transmembrane proteins that, in the nervous system, mediate repulsive signals of semaphorins.However, the molecular nature of plexin-mediated signal transduction remains poorly understood. Here, we demonstrate that plexin-B family members associate through their C termini with the Rho guanine nucleotide exchange factors PDZ-RhoGEF and LARG. Activation of plexin-B1 by semaphorin 4D regulates PDZ-RhoGEF/LARG activity leading to RhoA activation. In addition, a dominant-negative form of PDZ-RhoGEF blocks semaphorin 4D-induced growth cone collapse in primary hippocampal neurons. Our study indicates that the interaction of mammalian plexin-B family members with the multidomain proteins PDZ-RhoGEF and LARG represents an essential molecular link between plexin-B and localized, Rho-mediated downstream signaling events which underly various plexin-mediated cellular phenomena including axonal growth cone collapse.
引用
收藏
页码:51 / 63
页数:13
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