Thioredoxin-interacting protein regulates insulin transcription through microRNA-204

Nat Med. 2013 Sep;19(9):1141-6. doi: 10.1038/nm.3287. Epub 2013 Aug 25.

Abstract

Beta-cell dysfunction and impaired insulin production are hallmarks of diabetes, but despite the growing diabetes epidemic, the molecular mechanisms underlying this disease have remained unclear. We identified thioredoxin-interacting protein (TXNIP), a cellular redox regulator, as a crucial factor in beta-cell biology and show that beta-cell TXNIP is upregulated in diabetes, whereas TXNIP deficiency protects against diabetes by preventing beta-cell apoptosis. Here we show that TXNIP and diabetes induce beta-cell expression of a specific microRNA, miR-204, which in turn blocks insulin production by directly targeting and downregulating MAFA, a known insulin transcription factor. In particular, we first discovered the regulation of miR-204 by TXNIP by microarray analysis, followed by validation studies in INS-1 beta cells, islets of Txnip-deficient mice, diabetic mouse models and primary human islets. We then further found that TXNIP induces miR-204 by inhibiting the activity of signal transducer and activator of transcription 3 (STAT3), a transcription factor that is involved in miR-204 regulation. We also identified MAFA as a target that is downregulated by miR-204. Taken together, our results demonstrate that TXNIP controls microRNA expression and insulin production and that miR-204 is involved in beta-cell function. The newly identified TXNIP-miR-204-MAFA-insulin pathway may contribute to diabetes progression and provides new insight into TXNIP function and microRNA biology in health and disease.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism*
  • Diabetes Mellitus, Experimental / metabolism*
  • Humans
  • Insulin / genetics*
  • Insulin-Secreting Cells / metabolism
  • Maf Transcription Factors, Large / metabolism*
  • Male
  • Mice
  • Mice, Inbred C3H
  • Mice, Knockout
  • MicroRNAs / metabolism*
  • STAT3 Transcription Factor / antagonists & inhibitors
  • TRPM Cation Channels / metabolism
  • Thioredoxins / genetics
  • Thioredoxins / metabolism*
  • Transcription, Genetic
  • Up-Regulation

Substances

  • Carrier Proteins
  • Insulin
  • MIRN204 microRNA, mouse
  • Maf Transcription Factors, Large
  • Mafa protein, mouse
  • MicroRNAs
  • STAT3 Transcription Factor
  • Stat3 protein, mouse
  • TRPM Cation Channels
  • TRPM3 protein, mouse
  • Txnip protein, mouse
  • Thioredoxins