Sasaki Yukio, Cheng Chi, Uchida Yutaka, Nakajima Oumi, Ohshima Toshio, Yagi Takeshi, Taniguchi Masahiko, Nakayama Takashi, Kishida Reiji, Kudo Yoshihisa, Ohno Shigeaki, Nakamura Fumio, Goshima Yoshio
Department of Molecular Pharmacology and Neurobiology, Yokohama City University School of Medicine, Yokohama, Japan.
Neuron. 2002 Aug 29;35(5):907-20. doi: 10.1016/s0896-6273(02)00857-7.
Semaphorin-3A (Sema3A), a member of class 3 semaphorins, regulates axon and dendrite guidance in the nervous system. How Sema3A and its receptors plexin-As and neuropilins regulate neuronal guidance is unknown. We observed that in fyn- and cdk5-deficient mice, Sema3A-induced growth cone collapse responses were attenuated compared to their heterologous controls. Cdk5 is associated with plexin-A2 through the active state of Fyn. Sema3A promotes Cdk5 activity through phosphorylation of Tyr15, a phosphorylation site with Fyn. A Cdk5 mutant (Tyr15 to Ala) shows a dominant-negative effect on the Sema3A-induced collapse response. The sema3A gene shows strong interaction with fyn for apical dendrite guidance in the cerebral cortex. We propose a signal transduction pathway in which Fyn and Cdk5 mediate neuronal guidance regulated by Sema3A.
3型信号素(Semaphorin-3A,Sema3A)是3型信号素家族的一员,在神经系统中调节轴突和树突的导向。Sema3A及其受体丛状蛋白A(plexin-A)和神经纤毛蛋白如何调节神经元导向尚不清楚。我们观察到,在Fyn和Cdk5基因缺失的小鼠中,与野生型对照相比,Sema3A诱导的生长锥塌陷反应减弱。Cdk5通过Fyn的活性状态与丛状蛋白A2相关联。Sema3A通过Fyn的磷酸化位点Tyr15的磷酸化促进Cdk5的活性。一种Cdk5突变体(Tyr15突变为Ala)对Sema3A诱导的塌陷反应表现出显性负效应。Sema3A基因在大脑皮质顶端树突导向方面与Fyn表现出强烈的相互作用。我们提出了一条信号转导途径,其中Fyn和Cdk5介导由Sema3A调节的神经元导向。