Accelerated glucose intolerance, nephropathy, and atherosclerosis in prostaglandin D2 synthase knock-out mice

J Biol Chem. 2005 Aug 19;280(33):29946-55. doi: 10.1074/jbc.M502927200. Epub 2005 Jun 21.

Abstract

Type 2 diabetics have an increased risk of developing atherosclerosis, suggesting the mechanisms that cause this disease are enhanced by insulin resistance. In this study we examined the effects of gene knock-out (KO) of lipocalin-type prostaglandin D(2) synthase (L-PGDS), a protein found at elevated levels in type 2 diabetics, on diet-induced glucose tolerance and atherosclerosis. Our results show that L-PGDS KO mice become glucose-in-tolerant and insulin-resistant at an accelerated rate when compared with the C57BL/6 control strain. Adipocytes were significantly larger in the L-PGDS KO mice compared with controls on the same diets. Cell culture data revealed significant differences between insulin-stimulated mitogen-activated protein kinase phosphatase-2, protein-tyrosine phosphatase-1D, and phosphorylated focal adhesion kinase expression levels in L-PGDS KO vascular smooth muscle cells and controls. In addition, only the L-PGDS KO mice developed nephropathy and an aortic thickening reminiscent to the early stages of atherosclerosis when fed a "diabetogenic" high fat diet. We conclude that L-PGDS plays an important role regulating insulin sensitivity and atherosclerosis in type 2 diabetes and may represent a novel model of insulin resistance, atherosclerosis, and diabetic nephropathy.

Publication types

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

MeSH terms

  • Adipocytes / pathology
  • Adiponectin
  • Animals
  • Arteriosclerosis / etiology*
  • Blood Glucose / analysis
  • Diabetic Nephropathies / etiology*
  • Focal Adhesion Kinase 1
  • Focal Adhesion Protein-Tyrosine Kinases
  • Glucose Intolerance / etiology*
  • Insulin / blood
  • Insulin Resistance*
  • Intercellular Signaling Peptides and Proteins / blood
  • Intramolecular Oxidoreductases / deficiency
  • Intramolecular Oxidoreductases / physiology*
  • Lipocalins
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Protein Phosphatase 2
  • Protein Tyrosine Phosphatases / genetics
  • Protein-Tyrosine Kinases / genetics

Substances

  • Adiponectin
  • Blood Glucose
  • Insulin
  • Intercellular Signaling Peptides and Proteins
  • Lipocalins
  • Protein-Tyrosine Kinases
  • Focal Adhesion Kinase 1
  • Focal Adhesion Protein-Tyrosine Kinases
  • Ptk2 protein, mouse
  • Protein Phosphatase 2
  • Protein Tyrosine Phosphatases
  • Intramolecular Oxidoreductases
  • prostaglandin R2 D-isomerase