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PANCREATIC beta-CELL ELECTRICAL ACTIVITY AND INSULIN SECRETION: OF MICE AND MEN

期刊

PHYSIOLOGICAL REVIEWS
卷 98, 期 1, 页码 117-214

出版社

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/physrev.00008.2017

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资金

  1. Wellcome Trust [095551, 089795, 084655]
  2. European Research Council [322620]
  3. Royal Society
  4. Diabetes UK
  5. Medical Research Council
  6. Knut and Alice Wallenberg Foundation (Wallenberg Scholar Programme)
  7. Swedish Research Council
  8. Royal Society/Wolfson merit award
  9. BBSRC [BB/R002517/1, BB/R017220/1] Funding Source: UKRI
  10. MRC [G0801995, G0901521] Funding Source: UKRI

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The pancreatic beta-cell plays a key role in glucose homeostasis by secreting insulin, the only hormone capable of lowering the blood glucose concentration. Impaired insulin secretion results in the chronic hyperglycemia that characterizes type 2 diabetes (T2DM), which currently afflicts >450 million people worldwide. The healthy beta-cell acts as a glucose sensor matching its output to the circulating glucose concentration. It does so via metabolically induced changes in electrical activity, which culminate in an increase in the cytoplasmic Ca2+ concentration and initiation of Ca2+-dependent exocytosis of insulin-containing secretory granules. Here, we review recent advances in our understanding of the beta-cell transcriptome, electrical activity, and insulin exocytosis. We highlight salient differences between mouse and human beta-cells, provide models of how the different ion channels contribute to their electrical activity and insulin secretion, and conclude by discussing how these processes become perturbed in T2DM.

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