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嗜铬粒蛋白 A 和 B 作为囊泡货物和胞吐作用的调节剂。

Chromogranins A and B as regulators of vesicle cargo and exocytosis.

机构信息

Unit of Pharmacology, Medical School, La Laguna University, 38071 La Laguna, Tenerife, Spain.

出版信息

Cell Mol Neurobiol. 2010 Nov;30(8):1181-7. doi: 10.1007/s10571-010-9584-y. Epub 2010 Nov 3.

Abstract

Chromogranins (Cgs) are acidic proteins that have been implicated in several physiological processes such as vesicle sorting, the production of bioactive peptides and the accumulation of soluble species inside large dense core vesicles (LDCV). They constitute the main protein component in the vesicular matrix of LDCV. This latter characteristic of Cgs accounts for the ability of vesicles to concentrate catecholamines and Ca(2+). It is likely that Cgs are behind the delay in the neurotransmitter exit towards the extracellular milieu after vesicle fusion, due to their low affinity and high capacity to bind solutes present inside LDCV. The recent availability of mouse strains lacking Cgs, combined with the arrival of several techniques for the direct monitoring of exocytosis, have helped to expand our knowledge about the mechanisms used by granins to concentrate catecholamines and Ca(2+) in LDCV, and how they affect the kinetics of exocytosis. We will discuss the roles of Cgs A and B in maintaining the intravesicular environment of secretory vesicles and in exocytosis, bringing together the most recent findings from adrenal chromaffin cells.

摘要

嗜铬粒蛋白(Cgs)是酸性蛋白,参与多种生理过程,如囊泡分拣、生物活性肽的产生以及大致密芯囊泡(LDCV)内可溶性物质的积累。它们构成 LDCV 囊泡基质的主要蛋白质成分。Cgs 的这一特性解释了囊泡浓缩儿茶酚胺和 Ca(2+)的能力。由于 Cgs 与 LDCV 内溶质的亲和力低且结合容量高,因此在囊泡融合后,它们可能是导致神经递质向细胞外环境中释放延迟的原因。最近缺乏 Cgs 的小鼠品系的出现,结合几种直接监测胞吐作用的技术的出现,有助于扩展我们对颗粒蛋白用于在 LDCV 中浓缩儿茶酚胺和 Ca(2+)的机制以及它们如何影响胞吐作用动力学的认识。我们将讨论 Cgs A 和 B 在维持分泌囊泡的细胞内环境和胞吐作用中的作用,汇集来自肾上腺嗜铬细胞瘤的最新发现。

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