p24 family type 1 transmembrane proteins are required for insulin biosynthesis and secretion in pancreatic β-cells

被引:16
|
作者
Zhang, Liling [1 ]
Volchuk, Allen [1 ,2 ,3 ]
机构
[1] Univ Hlth Network, Toronto Gen Res Inst, Div Cellular & Mol Biol, Toronto, ON M5G 1L7, Canada
[2] Univ Toronto, Dept Biochem, Toronto, ON, Canada
[3] Univ Toronto, Dept Physiol, Toronto, ON, Canada
基金
加拿大健康研究院;
关键词
p24; protein; Insulin biosynthesis; Insulin secretion; Pancreatic beta-cell; ENDOPLASMIC-RETICULUM; MEMBRANE-PROTEIN; COATED VESICLES; TRANSPORT; ER; COMPONENT; COATOMER; MEMBERS; EMP24P; TRAFFICKING;
D O I
10.1016/j.febslet.2010.03.041
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
The p24 protein family have multiple functions in protein transport in the early secretory pathway. In this study we examined the role of p24 proteins in insulin transport. Several members were detected in insulinoma cell lines and rat islets and expression levels positively correlated with insulin abundance, particularly for p24 delta 1 and p24 beta 1. Knocking down p24 delta 1 in insulinoma cell lines, which also resulted in the concomitant knock-down of other family members, impaired glucose-stimulated insulin secretion, decreased total cellular insulin content and reduced proinsulin biosynthesis. There was no effect on overall protein biosynthesis or ER stress. These results suggest that p24 delta 1 and possibly other p24 family proteins are required for normal insulin biosynthesis and subsequent secretion in pancreatic beta-cells. (C) 2010 Federation of European Biochemical Societies. Published by Elsevier B. V. All rights reserved.
引用
收藏
页码:2298 / 2304
页数:7
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