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Insulin resistance in tetracycline-repressible Munc18c transgenic mice.

To investigate the physiological effects of modulating the abundance of Munc18c or syntaxin 4 (Syn4) proteins on the regulation of glucose homeostasis in vivo, we generated tetracycline-repressible transgenic mice that overexpress either Munc18c or Syn4 proteins in skeletal muscle, pancreas and adipose tissue seven-, five-, and threefold over endogenous protein, respectively. Munc18c transgenic mice displayed whole-body insulin resistance during hyperinsulinemic-euglycemic clamp resulting from >41% reductions in skeletal muscle and white adipose tissue glucose uptake, but without alteration of hepatic insulin action. Munc18c transgenic mice exhibited approximately 40% decreases in whole-body glycogen/lipid synthesis, skeletal muscle glycogen synthesis, and glycolysis. Glucose intolerance in Munc18c transgenic mice was reversed by repression of transgene expression using tetracycline or by simultaneous overexpression of Syn4 protein. In addition, Munc18c transgenic mice had depressed serum insulin levels, reflecting a threefold reduction in insulin secretion from islets isolated therefrom, thus uncovering roles for Munc18c and/or Syn4 in insulin granule exocytosis. Taken together, these results indicate that balance, more than absolute abundance, of Munc18c and Syn4 proteins directly affects whole-body glucose homeostasis through alterations in insulin secretion and insulin action.

Pubmed ID: 12882905


  • Spurlin BA
  • Thomas RM
  • Nevins AK
  • Kim HJ
  • Kim YJ
  • Noh HL
  • Shulman GI
  • Kim JK
  • Thurmond DC



Publication Data

August 28, 2003

Associated Grants

  • Agency: NIDDK NIH HHS, Id: R01 DK040936
  • Agency: NIDDK NIH HHS, Id: U24 DK-59635

Mesh Terms

  • Adipose Tissue
  • Animals
  • Anti-Bacterial Agents
  • Gene Expression
  • Glucose
  • Glucose Intolerance
  • Homeostasis
  • Insulin
  • Insulin Resistance
  • Membrane Proteins
  • Mice
  • Mice, Transgenic
  • Munc18 Proteins
  • Muscle, Skeletal
  • Nerve Tissue Proteins
  • Proteins
  • Qa-SNARE Proteins
  • Tetracycline
  • Vesicular Transport Proteins