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神经内分泌细胞中的胞吐作用:肌动蛋白的新任务

Exocytosis in neuroendocrine cells: new tasks for actin.

作者信息

Malacombe Magali, Bader Marie-France, Gasman Stéphane

机构信息

Département Neurotransmission et Sécrétion Neuroendocrine, Institut des Neurosciences Cellulaires et Intégratives (UMR 7168/LC2), Centre National de la Recherche Scientifique et Université Louis Pasteur, 5 rue Blaise Pascal, 67084 Strasbourg, France.

出版信息

Biochim Biophys Acta. 2006 Nov;1763(11):1175-83. doi: 10.1016/j.bbamcr.2006.09.004. Epub 2006 Sep 14.

Abstract

Most secretory cells undergoing calcium-regulated exocytosis in response to cell surface receptor stimulation display a dense subplasmalemmal actin network, which is remodeled during the exocytotic process. This review summarizes new insights into the role of the cortical actin cytoskeleton in exocytosis. Many earlier findings support the actin-physical-barrier model whereby transient depolymerization of cortical actin filaments permits vesicles to gain access to their appropriate docking and fusion sites at the plasma membrane. On the other hand, data from our laboratory and others now indicate that actin polymerization also plays a positive role in the exocytotic process. Here, we discuss the potential functions attributed to the actin cytoskeleton at each major step of the exocytotic process, including recruitment, docking and fusion of secretory granules with the plasma membrane. Moreover, we present actin-binding proteins, which are likely to link actin organization to calcium signals along the exocytotic pathway. The results cited in this review are derived primarily from investigations of the adrenal medullary chromaffin cell, a cell model that is since many years a source of information concerning the molecular machinery underlying exocytosis.

摘要

大多数因细胞表面受体刺激而经历钙调节性胞吐作用的分泌细胞,其质膜下会呈现出密集的肌动蛋白网络,该网络在胞吐过程中会发生重塑。本综述总结了关于皮质肌动蛋白细胞骨架在胞吐作用中作用的新见解。许多早期研究结果支持肌动蛋白物理屏障模型,即皮质肌动蛋白丝的瞬时解聚使囊泡能够到达其在质膜上合适的对接和融合位点。另一方面,我们实验室和其他实验室的数据现在表明,肌动蛋白聚合在胞吐过程中也发挥着积极作用。在这里,我们讨论了在胞吐过程的每个主要步骤中,肌动蛋白细胞骨架所具有的潜在功能,包括分泌颗粒与质膜的募集、对接和融合。此外,我们介绍了肌动蛋白结合蛋白,它们可能将肌动蛋白组织与沿胞吐途径的钙信号联系起来。本综述引用的结果主要来自对肾上腺髓质嗜铬细胞的研究,多年来,该细胞模型一直是有关胞吐作用分子机制信息的来源。

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