Cholesterol-enriched membrane rafts and insulin secretion

被引:22
作者
Dirkx, Ronald, Jr. [1 ,2 ]
Solimena, Michele [1 ,2 ,3 ]
机构
[1] Tech Univ Dresden, Paul Langerhans Inst Dresden, Sch Med, Dresden, Germany
[2] Tech Univ Dresden, Univ Clin Carl Gustav Carus, Dresden, Germany
[3] Max Planck Inst Mol Cell Biol & Genet, Dresden, Germany
关键词
Cholesterol; Pancreatic ss-cell; Type; 2; diabetes; PANCREATIC BETA-CELLS; SENSITIVE K+ CHANNELS; NITRIC-OXIDE SYNTHASE; LIPID RAFTS; GLUCOSE-HOMEOSTASIS; CARBOXYPEPTIDASE-E; SECRETOGRANIN-III; TRANSMEMBRANE DOMAIN; GRANULE MEMBRANE; CHROMOGRANIN-A;
D O I
10.1111/j.2040-1124.2012.00200.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The failure of pancreatic beta-cells to supply insulin in quantities sufficient to maintain euglycemia is a hallmark of type 2 diabetes. Perturbation of beta-cell cholesterol homeostasis, culminating in elevated intracellular cholesterol levels, impairs insulin secretion and has therefore been proposed as a mechanism contributing to beta-cell dysfunction. The manner in which this occurs, however, is unclear. Cholesterol is an essential lipid, as well as a major component of membrane rafts, and numerous proteins critical for the regulation of insulin secretion have been reported to associate with these domains. Although this suggests that alterations in membrane rafts could partially account for the reduction in insulin secretion observed when beta-cell cholesterol accumulates, this has not yet been demonstrated. In this review, we provide a brief overview of recent work implicating membrane rafts in some of the basic molecular mechanisms of insulin secretion, and discuss the insight it provides into the beta-cell dysfunction characteristic of type 2 diabetes. (J Diabetes Invest, doi: 10.1111/j.2040-1124.2012.00200.x, 2012)
引用
收藏
页码:339 / 346
页数:8
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