Epigenetic Regulation of Pancreatic Islets

被引:10
作者
Haumaitre, Cecile [1 ]
机构
[1] Univ Paris 06, INSERM, U969, CNRS,UMR 7622, F-75005 Paris, France
关键词
Epigenetics; Regulation; Endocrine cell differentiation; Beta-cell function; Methylation; Histone deacetylase; MicroRNA; Diabetes; Pancreatic islets; HISTONE DEACETYLASE INHIBITORS; GENOME-WIDE ANALYSIS; BETA-CELLS; DNA METHYLATION; MICRORNA EXPRESSION; ALPHA-CELL; CHROMATIN; GLUCOSE; GROWTH; PROLIFERATION;
D O I
10.1007/s11892-013-0403-y
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Epigenetic mechanisms, including DNA methylation, histone modifications, and noncoding RNA expression, contribute to regulate islet cell development and function. Indeed, epigenetic mechanisms were recently shown to be involved in the control of endocrine cell fate decision, islet differentiation, beta-cell identity, proliferation, and mature function. Epigenetic mechanisms can also contribute to the pathogenesis of complex diseases. Emerging knowledge regarding epigenetic mechanisms suggest that they may be involved in beta-cell dysfunction and pathogenesis of diabetes. Epigenetic mechanisms could predispose to the diabetic phenotype such as decline of beta-cell proliferation ability and beta-cell failure, and account for complications associated with diabetes. Better understanding of epigenetic landscapes of islet differentiation and function may be useful to improve beta-cell differentiation protocols and discover novel therapeutic targets for prevention and treatment of diabetes.
引用
收藏
页码:624 / 632
页数:9
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