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神经突生长多适配体RhoGAP,即NOMA-GAP,通过SHP2和Cdc42调节神经突延伸。

The neurite outgrowth multiadaptor RhoGAP, NOMA-GAP, regulates neurite extension through SHP2 and Cdc42.

作者信息

Rosário Marta, Franke Renate, Bednarski Christien, Birchmeier Walter

机构信息

Max Delbrück Center for Molecular Medicine, Berlin, Germany.

出版信息

J Cell Biol. 2007 Jul 30;178(3):503-16. doi: 10.1083/jcb.200609146.

Abstract

Neuronal differentiation involves the formation and extension of neuronal processes. We have identified a novel regulator of neurite formation and extension, the neurite outgrowth multiadaptor, NOMA-GAP, which belongs to a new family of multiadaptor proteins with RhoGAP activity. We show that NOMA-GAP is essential for NGF-stimulated neuronal differentiation and for the regulation of the ERK5 MAP kinase and the Cdc42 signaling pathways downstream of NGF. NOMA-GAP binds directly to the NGF receptor, TrkA, and becomes tyrosine phosphorylated upon receptor activation, thus enabling recruitment and activation of the tyrosine phosphatase SHP2. Recruitment of SHP2 is required for the stimulation of neuronal process extension and for sustained activation of ERK5 downstream of NOMA-GAP. In addition, we show that NOMA-GAP promotes neurite outgrowth by tempering activation of the Cdc42/PAK signaling pathway in response to NGF. NOMA-GAP, through its dual function as a multiadaptor and RhoGAP protein, thus plays an essential role downstream of NGF in promoting neurite outgrowth and extension.

摘要

神经元分化涉及神经元突起的形成和延伸。我们鉴定出一种神经突形成和延伸的新型调节因子——神经突生长多接头蛋白NOMA-GAP,它属于具有RhoGAP活性的多接头蛋白新家族。我们发现NOMA-GAP对于NGF刺激的神经元分化以及NGF下游ERK5丝裂原活化蛋白激酶和Cdc42信号通路的调节至关重要。NOMA-GAP直接与NGF受体TrkA结合,并在受体激活时发生酪氨酸磷酸化,从而能够募集和激活酪氨酸磷酸酶SHP2。募集SHP2是刺激神经元突起延伸以及NOMA-GAP下游ERK5持续激活所必需的。此外,我们发现NOMA-GAP通过调节对NGF的Cdc42/PAK信号通路激活来促进神经突生长。因此,NOMA-GAP作为多接头蛋白和RhoGAP蛋白的双重功能,在NGF下游促进神经突生长和延伸中起着至关重要的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d421/2064841/170756ef7678/jcb1780503f01.jpg

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