Lack of cholesterol mobilization in islets of hormone-sensitive lipase deficient mice impairs insulin secretion

被引:13
作者
Larsson, Sara [1 ]
Wierup, Nils [1 ]
Sundler, Frank [1 ]
Eliasson, Lena [2 ]
Holm, Cecilia [1 ]
机构
[1] Lund Univ, Dept Expt Med Sci, Div Endocrinol Diabet & Metab, SE-22184 Lund, Sweden
[2] Lund Univ, Dept Clin Sci, Div Islet Cell Exocytosis, Malmo, Sweden
基金
瑞典研究理事会;
关键词
Insulin secretion; Hormone-sensitive lipase; Cholesterol; beta-cells; Methyl-beta-cyclodextrin;
D O I
10.1016/j.bbrc.2008.09.045
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 observations that hormone-sensitive lipase (HSL) is located in close association to insulin granules in beta-cells and that cholesterol ester hydrolase activity is completely blunted in islets of HSL null mice made us hypothesize that the role of HSL in beta-cells is to Provide cholesterol for the exocytosis of insulin. To test this hypothesis, wild type (wt) and HSL null islets were depleted of plasma membrane cholesterol using methyl-beta-cyclodextrin (m beta cd). A significant reduction in insulin secretion from HSL null islets was observed whereas wt islets were unaffected. Using synaptosomal protein of 25 kDa (SNAP-25) as indicator of cholesterol-rich microdomains, confocal microscopy was used to show that HSL null beta-cells treated with m beta cd contained fewer clusters than wt beta-cells. These results indicate that HSL plays an important role in insulin secretion by providing free cholesterol for the formation and maintenance of cholesterol-rich patches for docking of SNARE-proteins to the plasma membrane. (c) 2008 Elsevier Inc. All rights reserved
引用
收藏
页码:558 / 562
页数:5
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