Granule docking and cargo release in pancreatic β-cells

被引:10
作者
Barg, Sebastian [1 ,2 ]
Lindqvist, Anders [2 ]
Obermuller, Stefanie [2 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Cell Biol, Div Med, London SW7 2AZ, England
[2] Lund Univ, Dept Clin Sci, Clin Res Ctr, SE-20502 Malmo, Sweden
关键词
docking; exocytosis; fusion pore; insulin secretory granule; live-cell imaging; syntaxin;
D O I
10.1042/BST0360294
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Biphasic insulin secretion is required for proper insulin action and is observed not only in vivo, but also in isolated pancreatic islets and even single beta-cells. Late events in the granule life cycle are thought to underlie this temporal pattern. In the last few years, we have therefore combined live cell imaging and electrophysiology to study insulin secretion at the level of individual granules, as they approach the plasma membrane, undergo exocytosis and finally release their insulin cargo. In the present paper, we review evidence for two emerging concepts that affect insulin secretion at the level of individual granules: (i) the existence of specialized sites where granules dock in preparation for exocytosis; and (ii) post-exocytotic regulation of cargo release by the fusion pore.
引用
收藏
页码:294 / 299
页数:6
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