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Nck衔接蛋白控制着对行走至关重要的神经回路的组织。

Nck adaptor proteins control the organization of neuronal circuits important for walking.

作者信息

Fawcett James P, Georgiou John, Ruston Julie, Bladt Friedhelm, Sherman Andrew, Warner Neil, Saab Bechara J, Scott Rizaldy, Roder John C, Pawson Tony

机构信息

Samuel Lunenfeld Research Institute, Mount Sinai Hospital, 600 University Avenue, Toronto, ON, Canada.

出版信息

Proc Natl Acad Sci U S A. 2007 Dec 26;104(52):20973-8. doi: 10.1073/pnas.0710316105. Epub 2007 Dec 18.

Abstract

The intracellular signaling targets used by mammalian axon guidance receptors to organize the nervous system in vivo are unclear. The Nck1 and Nck2 SH2/SH3 adaptors (collectively Nck) can couple phosphotyrosine (pTyr) signals to reorganization of the actin cytoskeleton and are therefore candidates for linking guidance cues to the regulatory machinery of the cytoskeleton. We find that selective inactivation of Nck in the murine nervous system causes a hopping gait and a defect in the spinal central pattern generator, which is characterized by synchronous firing of bilateral ventral motor neurons. Nck-deficient mice also show abnormal projections of corticospinal tract axons and defective development of the posterior tract of the anterior commissure. These phenotypes are consistent with a role for Nck in signaling initiated by different classes of guidance receptors, including the EphA4 receptor tyrosine kinase. Our data indicate that Nck adaptors couple pTyr guidance signals to cytoskeletal events required for the ipsilateral projections of spinal cord neurons and thus for normal limb movement.

摘要

哺乳动物轴突导向受体在体内构建神经系统时所使用的细胞内信号转导靶点尚不清楚。Nck1和Nck2 SH2/SH3衔接蛋白(统称为Nck)可将磷酸酪氨酸(pTyr)信号与肌动蛋白细胞骨架的重组相偶联,因此是将导向线索与细胞骨架调节机制相联系的候选分子。我们发现,在小鼠神经系统中选择性失活Nck会导致跳跃步态以及脊髓中枢模式发生器出现缺陷,其特征为双侧腹侧运动神经元同步放电。Nck缺陷型小鼠还表现出皮质脊髓束轴突投射异常以及前连合后束发育缺陷。这些表型与Nck在由不同类型导向受体(包括EphA4受体酪氨酸激酶)启动的信号转导中的作用一致。我们的数据表明,Nck衔接蛋白将pTyr导向信号与脊髓神经元同侧投射所需的细胞骨架事件相偶联,从而与正常肢体运动相偶联。

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