Circadian regulation of glucose homeostasis and insulin secretion has long been appreciated as an important feature of metabolic control in humans. Circadian disruption is becoming increasingly prevalent in today's society and is likely responsible in part for the considerable rise in type 2 diabetes (T2DM) and metabolic syndrome worldwide. Thus, understanding molecular mechanisms driving the inter-relationship between circadian disruption and T2DM is important in context of disease prevention and therapeutics. In this regard, the goal of this article is to highlight the role of the circadian system, and islet circadian clocks in particular, as potential regulators of -cell function and survival. To date, studies have shown that islet clocks respond to changes in feeding patterns, and regulate a multitude of critical cellular processes in insulin secreting -cells (e.g. insulin exocytosis, mitochondrial function and response to oxidative stress). Subsequently, either genetic or environmental disruption of normal islet clock performance compromises -cell function and leads to loss of glycaemic control. Future work is warranted to further unravel the role of circadian clocks in human islet function in health and contributions to pathogenesis of T2DM.
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Univ Manchester, Fac Life Sci, Manchester, Lancs, England
Univ Manchester, Wellcome Trust Ctr Cell Matrix Res, Manchester, Lancs, EnglandUniv Manchester, Fac Life Sci, Manchester, Lancs, England
Dudek, M.
Yang, N.
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Univ Manchester, Fac Life Sci, Manchester, Lancs, England
Univ Manchester, Wellcome Trust Ctr Cell Matrix Res, Manchester, Lancs, EnglandUniv Manchester, Fac Life Sci, Manchester, Lancs, England
Yang, N.
Ruckshanthi, J. P. D.
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Univ Manchester, Fac Life Sci, Manchester, Lancs, England
Univ Manchester, Wellcome Trust Ctr Cell Matrix Res, Manchester, Lancs, EnglandUniv Manchester, Fac Life Sci, Manchester, Lancs, England
Ruckshanthi, J. P. D.
Gossan, N.
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Univ Manchester, Fac Life Sci, Manchester, Lancs, EnglandUniv Manchester, Fac Life Sci, Manchester, Lancs, England
Gossan, N.
Im, H. -J.
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Rush Univ, Med Ctr, Jesse Brown VA Med Ctr, Dept Biochem, Chicago, IL 60612 USAUniv Manchester, Fac Life Sci, Manchester, Lancs, England
Im, H. -J.
Fukada, Y.
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Univ Tokyo, Dept Biol Sci, Tokyo, JapanUniv Manchester, Fac Life Sci, Manchester, Lancs, England
Fukada, Y.
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Yagita, K.
Bateman, J. F.
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Murdoch Childrens Res Inst, Parkville, Vic, AustraliaUniv Manchester, Fac Life Sci, Manchester, Lancs, England
Bateman, J. F.
Boot-Handford, R. P.
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Univ Manchester, Wellcome Trust Ctr Cell Matrix Res, Manchester, Lancs, EnglandUniv Manchester, Fac Life Sci, Manchester, Lancs, England
Boot-Handford, R. P.
Hoyland, J. A.
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Univ Manchester, Fac Med & Human Sci, Manchester, Lancs, England
Manchester Acad Hlth Sci Ctr, NIHR Manchester Musculoskeletal Biomed Res Unit, Manchester, Lancs, EnglandUniv Manchester, Fac Life Sci, Manchester, Lancs, England
Hoyland, J. A.
Meng, Q. -J.
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Univ Manchester, Fac Life Sci, Manchester, Lancs, England
Univ Manchester, Wellcome Trust Ctr Cell Matrix Res, Manchester, Lancs, EnglandUniv Manchester, Fac Life Sci, Manchester, Lancs, England