KATP channels and insulin secretion:: a key role in health and disease

被引:78
作者
Ashcroft, FM [1 ]
机构
[1] Univ Oxford, Univ Lab Pathol, Oxford OX1 3PT, England
关键词
ATP-sensitive potassium channel (K-ATP channel); diabetes; insulin secretion; Kir6.2; nicotinamide nucleoitide transhydrogenase (Nnt); sulphonylurea;
D O I
10.1042/BST0340243
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
This review summarizes advances in our understanding of the structure and function of the ATP-sensitive potassium (K-ATP) channel of the pancreatic beta-cell that have been made over the last 5 years. it discusses recent structural studies of the octameric K-ATP, channel complex and studies of the regulation of KATP channel activity by nucleotides. it then considers the molecular mechanism by which gain-of-function mutations in the Kir6.2 subunit of the K-ATP channel reduce channel inhibition by ATP and thereby lead to neonatal diabetes, and how identification of these mutations has led to changes in therapy. Finally, it illustrates how mouse models of glucose intolerance or diabetes can provide fresh insight into beta-cell function, using the C57BL/6J mouse, whose glucose intolerance arises from mutations in nicotinamide nucleotide transhydrogenase, as an example.
引用
收藏
页码:243 / 246
页数:4
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