Autocrine anti-apoptotic and proliferative effects of insulin in pancreatic β-cells

被引:52
作者
Muller, Dany [1 ]
Jones, Peter M. [1 ]
Persaud, Shanta J. [1 ]
机构
[1] Kings Coll London, Sch Biomed & Hlth Sci, Beta Cell Dev & Funct Grp, London SE1 1UL, England
关键词
pancreatic beta-cell; apoptosis; proliferation; insulin; autocrine; PI-3; kinase;
D O I
10.1016/j.febslet.2006.11.066
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
Insulin and glucose inhibited apoptosis in the MIN6 insulin-secreting cell line. The protective effect of 25 mM glucose was prevented by an anti-insulin antibody and this antibodyinduced increase in apoptosis was reversed by the presence of excess insulin. Glucose stimulated MIN6 cell proliferation and this was inhibited by blockade of insulin secretion, by an anti-insulin antibody and by phosphatidylinositol-3 kinase (PI-3K) inhibition. Furthermore, MIN6 cell proliferation was stimulated by depolarising concentrations of KCI and by insulin itself. These data indicate that insulin secreted by beta-cells in response to elevated glucose exerts autocrine effects to protect against apoptosis and stimulate proliferation, and suggest that the insulin signalling cascade, through the PI-3K pathway, may be an effective means of maintaining beta-cell mass in diabetes. (c) 2006 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:6977 / 6980
页数:4
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