Hyperglycemia repression of miR-24 coordinately upregulates endothelial cell expression and secretion of von Willebrand factor

Blood. 2015 May 28;125(22):3377-87. doi: 10.1182/blood-2015-01-620278. Epub 2015 Mar 26.


An elevated level of von Willebrand factor (VWF) in diabetic patients is associated with increased risk of thrombotic cardiovascular events. The underlying mechanism of how VWF expression is upregulated in diabetes mellitus is poorly understood. We now report that hyperglycemia-induced repression of microRNA-24 (miR-24) increases VWF expression and secretion in diabetes mellitus. In diabetic patients and diabetic mouse models (streptozotocin/high-fat diet-induced and db/db mice), miR-24 is reduced in both tissues and plasma. Knockdown of miR-24 in mice leads to increased VWF mRNA and protein levels and enhanced platelet tethering (spontaneous thrombosis). miR-24 tightly controls VWF levels through pleiotropic effects, including direct binding to the 3' untranslated region of VWF and targeting FURIN and the histamine H1 receptor, known regulators of VWF processing and secretion in endothelial cells. We present a novel mechanism for miR-24 downregulation through hyperglycemia-induced activation of aldose reductase, reactive oxygen species, and c-Myc. These findings support a critical role for hyperglycemic repression of miR-24 in VWF-induced pathology. miR-24 represents a novel therapeutic target to prevent adverse thrombotic events in patients with diabetes mellitus.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Case-Control Studies
  • Diabetes Mellitus / genetics
  • Diabetes Mellitus / metabolism
  • Diabetic Angiopathies / genetics
  • Diabetic Angiopathies / metabolism
  • Down-Regulation / genetics
  • Endothelial Cells / metabolism*
  • Female
  • Gene Expression Regulation
  • Humans
  • Hyperglycemia / genetics*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • MicroRNAs / genetics*
  • von Willebrand Factor / genetics*
  • von Willebrand Factor / metabolism*


  • MIRN24 microRNA, human
  • MicroRNAs
  • von Willebrand Factor