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ATP敏感性钾通道亚基Kir6.2突变诱发的糖尿病

Research Dvelopment on Diabetes Induced by Kir6. 2 Mutation
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摘要 Kit6.2是细胞膜和线粒体膜上KATP通道的组成亚基,存在于胰岛、心肌、骨骼肌、脑等组织中。在胰岛β细胞中,Kit6.2亚基是调节胰岛素分泌的重要因子,Kir6.2的突变会导致新生儿糖尿病、婴儿高胰岛素性低血糖症和2型糖尿病等3种糖尿病的发生。文章综述了近年来有关Kir6.2突变导致的多种糖尿病的研究进展。以期对人们了解Kit6.2亚基的功能和科研人员进一步研究糖尿病的治疗有所帮助。 Kit6. 2 is a constituted subunit of KATP in cell membrane and endo-plasmic reticulum membrane, existed in tissues, such as pancreatic islets, cardiac muscle, brain and so on. In pancreatic β cells, Kit6. 2 is a key component of regulating insulin secretion, the mutation of kir6. 2 induces neonatal diabetes mellitus (NDM) , Persistent hyperinsulinemic hypoglycemia of infancy (PHHI) and type2 diabetes (T2DM) . Our review focuses on the research advance of several kinds of diabetes induced by Kir6. 2 mutation, which intends to promote the study of the function of Kir6. 2 and the further research of the diabetes therapy.
出处 《医学分子生物学杂志》 CAS CSCD 2010年第4期346-350,共5页 Journal of Medical Molecular Biology
基金 资助项目:国家自然科学基金(No.50603032)
关键词 Kit6.2突变 糖尿病 KATP通道 Kir6. 2 mutation diabetes KATP channel
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