C-peptide prevents hyperglycemia-induced endothelial apoptosis through inhibition of reactive oxygen species-mediated transglutaminase 2 activation

Diabetes. 2013 Jan;62(1):243-53. doi: 10.2337/db12-0293. Epub 2012 Aug 24.

Abstract

C-peptide is a bioactive peptide with a potentially protective role in diabetes complications; however, its molecular mechanism of protection against cardiovascular damage caused by hyperglycemia-induced apoptosis remains unclear. We investigated the protective mechanism of C-peptide against hyperglycemia-induced apoptosis using human umbilical vein endothelial cells and streptozotocin diabetic mice. High glucose (33 mmol/L) induced apoptotic cell death in endothelial cells via sequential elevation of intracellular Ca(2+) and reactive oxygen species (ROS) as well as subsequent activation of transglutaminase 2 (TG2). C-peptide (1 nmol/L) prevented endothelial cell death by inhibiting protein kinase C- and NADPH oxidase-dependent intracellular ROS generation and by abolishing high glucose-induced TG2 activation, without affecting intracellular Ca(2+) levels. Consistently, in the aorta of streptozotocin diabetic mice, hyperglycemia stimulated transamidating activity and endothelial cell apoptosis that was inhibited by C-peptide replacement therapy (35 pmol/min/kg) using osmotic pumps (control and diabetes, n = 8; diabetes + C-peptide, n = 7). In addition, C-peptide prevented hyperglycemia-induced activation of transamidation activity and apoptosis in the heart and renal cortex of streptozotocin diabetic mice. Thus, C-peptide protects endothelial cells from hyperglycemia-induced apoptotic cell death by inhibiting intracellular ROS-mediated activation of TG2. Furthermore, TG2 may be a promising avenue of therapeutic investigation to treat diabetic vasculopathies.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis*
  • C-Peptide / physiology*
  • Calcium / metabolism
  • Cells, Cultured
  • Diabetes Mellitus, Experimental / metabolism
  • Diabetes Mellitus, Experimental / pathology
  • Enzyme Activation
  • GTP-Binding Proteins / antagonists & inhibitors
  • GTP-Binding Proteins / physiology*
  • Human Umbilical Vein Endothelial Cells / pathology*
  • Humans
  • Hyperglycemia / pathology*
  • Kidney Cortex / pathology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Myocardium / pathology
  • Protein Glutamine gamma Glutamyltransferase 2
  • Reactive Oxygen Species / metabolism*
  • Streptozocin
  • Transglutaminases / antagonists & inhibitors
  • Transglutaminases / physiology*

Substances

  • C-Peptide
  • Reactive Oxygen Species
  • Streptozocin
  • Protein Glutamine gamma Glutamyltransferase 2
  • Transglutaminases
  • GTP-Binding Proteins
  • Calcium