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胞吐作用的机制

Mechanisms of exocytosis.

作者信息

Sugita S

机构信息

Division of Fundamental Neurobiology, Toronto Western Research Institute, University Health Network and Department of Physiology, University of Toronto, Toronto, ON, Canada.

出版信息

Acta Physiol (Oxf). 2008 Feb;192(2):185-93. doi: 10.1111/j.1748-1716.2007.01803.x. Epub 2007 Nov 15.

Abstract

Catecholamines and peptides secreted from dense-core vesicles (DCVs) of adrenal chromaffin cells regulate a wide variety of physiological processes. For instance, the release of noradrenaline and adrenaline plays a key role in regulating heart rate and blood pressure. Thus understanding the mechanisms of secretory processes of DCVs is crucial for understanding the basis of diseases such as hypertension. DCVs undergo several stages of secretory processing before they are exocytosed. These include docking, priming and triggering of membrane fusion/exocytosis. Molecular studies of DCV exocytosis have identified many proteins critically involved in DCV secretion. These proteins include SNARE proteins, Munc18-1, phosphatidylinositol transfer protein, type I phosphatidylinositol-4-phosphate-5-kinases, NSF, Munc13, CAPS1, synaptotagmins, RalA/RalB GTPases and exocyst proteins. In this article, I will discuss the functions of these proteins within the context of the stages (i.e. docking, priming and triggering of membrane fusion/exocytosis) in DCV secretion.

摘要

肾上腺嗜铬细胞致密核心囊泡(DCV)分泌的儿茶酚胺和肽类调节着多种生理过程。例如,去甲肾上腺素和肾上腺素的释放对调节心率和血压起着关键作用。因此,了解DCV分泌过程的机制对于理解诸如高血压等疾病的发病基础至关重要。DCV在胞吐之前会经历几个分泌加工阶段。这些阶段包括对接、引发以及膜融合/胞吐的触发。对DCV胞吐作用的分子研究已经鉴定出许多在DCV分泌中起关键作用的蛋白质。这些蛋白质包括可溶性N-乙基马来酰亚胺敏感因子附着蛋白受体(SNARE)蛋白、Munc18-1、磷脂酰肌醇转移蛋白、I型磷脂酰肌醇-4-磷酸-5-激酶、N-乙基马来酰亚胺敏感因子(NSF)、Munc13、Ca2+结合蛋白1(CAPS1)、突触结合蛋白、RalA/RalB小GTP酶以及外排复合体蛋白。在本文中,我将在DCV分泌的各个阶段(即对接、引发以及膜融合/胞吐的触发)的背景下讨论这些蛋白质的功能。

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