Timp3 deficiency in insulin receptor-haploinsufficient mice promotes diabetes and vascular inflammation via increased TNF-alpha

J Clin Invest. 2005 Dec;115(12):3494-505. doi: 10.1172/JCI26052. Epub 2005 Nov 17.

Abstract

Activation of inflammatory pathways may contribute to the beginning and the progression of both atherosclerosis and type 2 diabetes. Here we report a novel interaction between insulin action and control of inflammation, resulting in glucose intolerance and vascular inflammation and amenable to therapeutic modulation. In insulin receptor heterozygous (Insr+/-) mice, we identified the deficiency of tissue inhibitor of metalloproteinase 3 (Timp3, an inhibitor of both TNF-alpha-converting enzyme [TACE] and MMPs) as a common bond between glucose intolerance and vascular inflammation. Among Insr+/- mice, those that develop diabetes have reduced Timp3 and increased TACE activity. Unchecked TACE activity causes an increase in levels of soluble TNF-alpha, which subsequently promotes diabetes and vascular inflammation. Double heterozygous Insr+/-Timp3+/- mice develop mild hyperglycemia and hyperinsulinemia at 3 months and overt glucose intolerance and hyperinsulinemia at 6 months. A therapeutic role for Timp3/TACE modulation is supported by the observation that pharmacological inhibition of TACE led to marked reduction of hyperglycemia and vascular inflammation in Insr+/- diabetic mice, as well as by the observation of increased insulin sensitivity in Tace+/- mice compared with WT mice. Our results suggest that an interplay between reduced insulin action and unchecked TACE activity promotes diabetes and vascular inflammation.

Publication types

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

MeSH terms

  • Analysis of Variance
  • Animals
  • Deoxyglucose / metabolism
  • Diabetes Mellitus / pathology
  • Electrophoresis, Polyacrylamide Gel
  • Gene Expression Profiling
  • Genetic Vectors
  • Glucose / metabolism
  • Glucose Tolerance Test
  • Glycogen / chemistry
  • Heterozygote
  • Homeostasis
  • Hyperglycemia / pathology
  • Hyperinsulinism / pathology
  • Inflammation / genetics*
  • Insulin / metabolism
  • Liver / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Muscle, Skeletal / pathology
  • Muscles / pathology
  • Phosphorylation
  • Promoter Regions, Genetic
  • Protein Binding
  • RNA / chemistry
  • RNA / metabolism
  • RNA, Messenger / metabolism
  • RNA, Small Interfering / metabolism
  • Receptor, Insulin / metabolism*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Signal Transduction
  • Time Factors
  • Tissue Inhibitor of Metalloproteinase-3 / genetics*
  • Tissue Inhibitor of Metalloproteinase-3 / metabolism
  • Tissue Inhibitor of Metalloproteinase-3 / physiology*
  • Tumor Necrosis Factor-alpha / genetics*
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Insulin
  • RNA, Messenger
  • RNA, Small Interfering
  • Tissue Inhibitor of Metalloproteinase-3
  • Tumor Necrosis Factor-alpha
  • RNA
  • Glycogen
  • Deoxyglucose
  • Receptor, Insulin
  • Glucose