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整合素-细胞外基质相互作用对轴突生长和导向的调控。

Regulation of axonal outgrowth and pathfinding by integrin-ECM interactions.

机构信息

Department of Neuroscience, Neuroscience Training Program, University of Wisconsin, Madison, Wisconsin 53706, USA.

出版信息

Dev Neurobiol. 2011 Nov;71(11):901-23. doi: 10.1002/dneu.20931.

Abstract

Developing neurons use a combination of guidance cues to assemble a functional neural network. A variety of proteins immobilized within the extracellular matrix (ECM) provide specific binding sites for integrin receptors on neurons. Integrin receptors on growth cones associate with a number of cytosolic adaptor and signaling proteins that regulate cytoskeletal dynamics and cell adhesion. Recent evidence suggests that soluble growth factors and classic axon guidance cues may direct axon pathfinding by controlling integrin-based adhesion. Moreover, because classic axon guidance cues themselves are immobilized within the ECM and integrins modulate cellular responses to many axon guidance cues, interactions between activated receptors modulate cell signals and adhesion. Ultimately, growth cones control axon outgrowth and pathfinding behaviors by integrating distinct biochemical signals to promote the proper assembly of the nervous system. In this review, we discuss our current understanding how ECM proteins and their associated integrin receptors control neural network formation.

摘要

发育中的神经元利用一系列导向线索来组装功能性神经网络。细胞外基质(ECM)中固定的多种蛋白质为神经元上的整合素受体提供了特定的结合位点。生长锥上的整合素受体与许多胞质衔接蛋白和信号蛋白结合,这些蛋白调节细胞骨架动力学和细胞黏附。最近的证据表明,可溶性生长因子和经典的轴突导向线索可能通过控制基于整合素的黏附来指导轴突寻路。此外,由于经典的轴突导向线索本身固定在细胞外基质中,并且整合素调节细胞对许多轴突导向线索的反应,因此激活受体之间的相互作用调节细胞信号和黏附。最终,生长锥通过整合不同的生化信号来控制轴突生长和寻路行为,以促进神经系统的正确组装。在这篇综述中,我们讨论了我们目前对 ECM 蛋白及其相关整合素受体如何控制神经网络形成的理解。

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