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有部分调节的胞吐作用。

Regulated exocytosis per partes.

出版信息

Cell Calcium. 2012 Sep-Oct;52(3-4):191-5. doi: 10.1016/j.ceca.2012.06.003. Epub 2012 Jul 9.

DOI:10.1016/j.ceca.2012.06.003
PMID:22784668
Abstract

This Special Issue (SI) of Cell Calcium focuses on regulated exocytosis, a recent evolutionary invention of eukaryotic cells. This essential cellular process consists of several stages: (i) the delivery of membrane bound vesicles to specific plasma membrane sites, (ii) where the merger between the vesicle and the plasma membranes occurs, (iii) leading to the formation of an aqueous channel through which vesicle content starts to be discharged to the cell exterior, (iv) after the full incorporation of the vesicle membrane into the plasma membrane, the added vesicle membrane is retrieved back into the cytoplasm by endocytosis. (v) When a fusion pore opens it may close again, a process known as transient fusion pore opening (also kiss-and-run exocytosis). In some cell types these stages are extremely shortlived, as in some neurons, and thus relatively inaccessible to experimentation. In other cell types the transition between these stages is orders of magnitude slower and can be studied in more detail. However, despite the intense investigations of this critical biological process over the last decades, the molecular mechanisms underlying regulated exocytosis have yet to be fully resolved. We thus still lack a comprehensive physiological insight into the nature of the progressive and coupled stages of exocytosis. Such a molecular-level understanding would help to fully reconstruct this process in vitro, as well as identify potential therapeutic targets for a range of diseases and dysfunctions. There are 18 papers in this SI which have been organized into three sections: Rapid regulated exocytosis and calcium homeostasis with an introduction by Erwin Neher, Molecular mechanisms of regulated exocytosis, and Cell models for regulated exocytosis. Here we briefly outline and integrate the messages of these sections.

摘要

本期细胞钙专刊聚焦于受调控的胞吐作用,这是真核细胞最近进化的发明。这个基本的细胞过程包含几个阶段:(i) 将膜结合囊泡输送到特定的质膜位点,(ii) 囊泡与质膜融合发生的位置,(iii) 导致形成一个水通道,囊泡内容物开始从细胞内部排出到细胞外部,(iv) 当囊泡膜完全融入质膜后,通过内吞作用将添加的囊泡膜回收回细胞质中。(v) 当融合孔打开时,它可能会再次关闭,这个过程称为短暂融合孔开放(也称为吻-跑胞吐作用)。在一些细胞类型中,这些阶段极其短暂,如在一些神经元中,因此相对难以进行实验研究。在其他细胞类型中,这些阶段之间的转变要慢几个数量级,可以更详细地研究。然而,尽管在过去几十年中对这个关键的生物学过程进行了深入的研究,但调节胞吐作用的分子机制尚未完全解决。因此,我们仍然缺乏对胞吐作用的渐进和偶联阶段的全面生理学认识。这种分子水平的理解将有助于在体外完全重建这个过程,并确定一系列疾病和功能障碍的潜在治疗靶点。本期专刊共有 18 篇论文,分为三个部分:快速调节胞吐作用和钙稳态,由 Erwin Neher 撰写引言;调节胞吐作用的分子机制;以及调节胞吐作用的细胞模型。在这里,我们简要概述并整合了这些部分的信息。

相似文献

1
Regulated exocytosis per partes.有部分调节的胞吐作用。
Cell Calcium. 2012 Sep-Oct;52(3-4):191-5. doi: 10.1016/j.ceca.2012.06.003. Epub 2012 Jul 9.
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Fusion pores, SNAREs, and exocytosis.融合孔、SNARE 蛋白和胞吐作用。
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SNARE-mediated vesicle navigation, vesicle anatomy and exocytotic fusion pore.SNARE 介导的囊泡运输、囊泡解剖学和胞吐融合孔。
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Cholesterol and regulated exocytosis: a requirement for unitary exocytotic events.胆固醇与调节性胞吐作用:单位胞吐事件的必需条件。
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Exocytotic fusion pore stability and topological defects in the membrane with orientational degree of ordering.具有取向有序度的膜中的胞吐融合孔稳定性和拓扑缺陷。
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引用本文的文献

1
Exocytotic fusion pore under stress.应激状态下的胞吐融合孔
Cell Stress. 2020 Aug 10;4(9):218-226. doi: 10.15698/cst2020.09.230.
2
Exocytotic pore in a SNARE.SNARE 中的胞吐孔道。
Oncotarget. 2017 Jun 13;8(24):38082-38083. doi: 10.18632/oncotarget.17511.
3
Astrocytes as secretory cells of the central nervous system: idiosyncrasies of vesicular secretion.星形胶质细胞作为中枢神经系统的分泌细胞:囊泡分泌的特性
EMBO J. 2016 Feb 1;35(3):239-57. doi: 10.15252/embj.201592705. Epub 2016 Jan 12.
4
Local electrostatic interactions determine the diameter of fusion pores.局部静电相互作用决定融合孔的直径。
Channels (Austin). 2015;9(2):96-101. doi: 10.1080/19336950.2015.1007825.
5
cAMP-mediated stabilization of fusion pores in cultured rat pituitary lactotrophs.cAMP 介导的培养的大鼠垂体泌乳素细胞融合孔的稳定化。
J Neurosci. 2013 May 1;33(18):8068-78. doi: 10.1523/JNEUROSCI.5351-12.2013.