4.6 Article

MiR-184 regulates insulin secretion through repression of Slc25a22

期刊

PEERJ
卷 1, 期 -, 页码 -

出版社

PEERJ INC
DOI: 10.7717/peerj.162

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miRNA; Insulin; Diabetes

资金

  1. Ministry of Education, Culture, Sports, Science and Technology of Japan
  2. Ministry of Health, Labour and Welfare of Japan
  3. National Institute of Biomedical Innovation
  4. Takeda Science Foundation

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Insulin secretion from pancreatic beta-cells plays an essential role in blood glucose homeostasis and type 2 diabetes. Many genes are involved in the secretion of insulin and most of these genes can be targeted by microRNAs (miRNAs). However, the role of miRNAs in insulin secretion and type 2 diabetes has not been exhaustively studied. The expression miR-184, a miRNA enriched in pancreatic islets, negatively correlates with insulin secretion, suggesting that it is a good candidate for miRNA-mediated regulation of insulin secretion. Here we report that miR-184 inhibits insulin secretion in the MIN6 pancreatic beta-cell line through the repression of its target Slc25a22, a mitochondrial glutamate carrier. Our study provides new insight into the regulation of insulin secretion by glutamate transport in mitochondria.

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