Unidad de Farmacología, Facultad de Medicina, Universidad de La Laguna, Tenerife, Spain.
J Neurochem. 2010 Jul;114(2):335-43. doi: 10.1111/j.1471-4159.2010.06786.x. Epub 2010 Apr 29.
Chromogranins (Cgs) constitute the main protein component in the vesicular matrix of large dense core vesicles (LDCV). These acidic proteins have been implicated in several physiological processes such as vesicle sorting, the generation of bioactive peptides and the accumulation of soluble species inside LDCV. This latter feature of Cgs accounts for the ability of vesicles to concentrate catecholamines and Ca(2+). Indeed, the low affinity and high capacity of Cgs to bind solutes at the low pH of the LDCV lumen seems to be behind the delay in the neurotransmitter exit towards the extracellular milieu after vesicle fusion. The availability of new mouse strains lacking Cgs in combination with the arrival of several techniques for the direct monitoring of exocytosis (like amperometry, patch-amperometry and intracellular electrochemistry), have helped advance our understanding of how these granins concentrate catecholamines and Ca(2+) in LDCV, and how they influence the kinetics of exocytosis. In this review, 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.
嗜铬粒蛋白(Cgs)构成大致密核心囊泡(LDCV)囊泡基质中的主要蛋白成分。这些酸性蛋白参与了多种生理过程,如囊泡分拣、生物活性肽的产生以及可溶性物质在 LDCV 内的积累。Cgs 的这一特性使得囊泡能够浓缩儿茶酚胺和 Ca(2+)。事实上,Cgs 在 LDCV 腔低 pH 下对溶质的低亲和力和高结合容量似乎是囊泡融合后神经递质向细胞外环境释放延迟的原因。缺乏 Cgs 的新型小鼠品系的出现,结合几种直接监测胞吐作用的技术(如安培法、膜片钳安培法和细胞内电化学)的出现,有助于我们深入了解这些颗粒如何在 LDCV 中浓缩儿茶酚胺和 Ca(2+),以及它们如何影响胞吐作用的动力学。在这篇综述中,我们将讨论 Cgs A 和 B 在维持分泌囊泡的囊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。