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通过粘附表面的蛋白水解重塑来调节突触。

Tuning synapses by proteolytic remodeling of the adhesive surface.

作者信息

Shinoe Toru, Goda Yukiko

机构信息

RIKEN Brain Science Institute, Wako, Saitama, 351-0198, Japan.

RIKEN Brain Science Institute, Wako, Saitama, 351-0198, Japan.

出版信息

Curr Opin Neurobiol. 2015 Dec;35:148-55. doi: 10.1016/j.conb.2015.08.005. Epub 2015 Aug 27.

Abstract

Cell adhesion molecules (CAMs) play a crucial role in organizing the synaptic interface and regulating synapse activity. In turn, CAMs can influence a variety of higher brain functions. In addition to their bona fide interacting partners on the apposed cell surface or the extracellular matrix (ECM) with which they form molecular bridges, synaptic CAMs bind to many other proteins with their intracellular and extracellular domains. The resulting multi-molecular complexes at the active zone and at the postsynaptic density (PSD) are thought to anchor components requisite for synaptic transmission. Recent studies demonstrating the proteolytic cleavage of synaptic CAMs underscore an exciting mechanism through which the synaptic microenvironment can be altered and thereby finely tune the efficacy of synaptic transmission.

摘要

细胞黏附分子(CAMs)在组织突触界面和调节突触活动中起着至关重要的作用。反过来,细胞黏附分子可以影响多种高级脑功能。除了在相邻细胞表面或细胞外基质(ECM)上与之形成分子桥的真正相互作用伙伴外,突触细胞黏附分子还通过其细胞内和细胞外结构域与许多其他蛋白质结合。在活性区和突触后致密部(PSD)形成的多分子复合物被认为是突触传递所需成分的锚定物。最近关于突触细胞黏附分子蛋白水解切割的研究强调了一种令人兴奋的机制,通过该机制可以改变突触微环境,从而精确调节突触传递的效能。

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