Deletion of cd39/entpd1 results in hepatic insulin resistance

Diabetes. 2008 Sep;57(9):2311-20. doi: 10.2337/db07-1265. Epub 2008 Jun 20.

Abstract

Objective: Extracellular nucleotides are important mediators of inflammatory responses and could also impact metabolic homeostasis. Type 2 purinergic (P2) receptors bind extracellular nucleotides and are expressed by major peripheral tissues responsible for glucose homeostasis. CD39/ENTPD1 is the dominant vascular and immune cell ectoenzyme that hydrolyzes extracellular nucleotides to regulate purinergic signaling.

Research design and methods: We have studied Cd39/Entpd1-null mice to determine whether any associated changes in extracellular nucleotide concentrations influence glucose homeostasis.

Results: Cd39/Entpd1-null mice have impaired glucose tolerance and decreased insulin sensitivity with significantly higher plasma insulin levels. Hyperinsulinemic-euglycemic clamp studies indicate altered hepatic glucose metabolism. These effects are mimicked in vivo by injection into wild-type mice of either exogenous ATP or an ecto-ATPase inhibitor, ARL-67156, and by exposure of hepatocytes to extracellular nucleotides in vitro. Increased serum interleukin-1beta, interleukin-6, interferon-gamma, and tumor necrosis factor-alpha levels are observed in Cd39/Entpd1-null mice in keeping with a proinflammatory phenotype. Impaired insulin sensitivity is accompanied by increased activation of hepatic c-Jun NH(2)-terminal kinase/stress-activated protein kinase in Cd39/Entpd1 mice after injection of ATP in vivo. This results in decreased tyrosine phosphorylation of insulin receptor substrate-2 with impeded insulin signaling.

Conclusions: CD39/Entpd1 is a modulator of extracellular nucleotide signaling and also influences metabolism. Deletion of Cd39/Entpd1 both directly and indirectly impacts insulin regulation and hepatic glucose metabolism. Extracellular nucleotides serve as "metabolokines," indicating further links between inflammation and associated metabolic derangements.

Publication types

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

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Adenosine Triphosphate / pharmacology
  • Adipose Tissue, Brown / immunology
  • Adipose Tissue, Brown / metabolism
  • Animals
  • Antigens, CD / genetics*
  • Antigens, CD / immunology*
  • Apyrase / genetics*
  • Apyrase / immunology*
  • Blood Glucose / metabolism
  • Cells, Cultured
  • Cytokines / blood
  • Energy Metabolism / physiology
  • Glucose Clamp Technique
  • Hepatocytes / cytology
  • Hepatocytes / immunology
  • Hepatocytes / metabolism
  • Hyperinsulinism / immunology
  • Hyperinsulinism / physiopathology
  • Insulin / blood
  • Insulin Receptor Substrate Proteins
  • Insulin Resistance / immunology*
  • Intracellular Signaling Peptides and Proteins / metabolism
  • JNK Mitogen-Activated Protein Kinases / metabolism
  • Liver / cytology
  • Liver / immunology
  • Liver / metabolism*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Muscle, Skeletal / immunology
  • Muscle, Skeletal / metabolism
  • Oxygen Consumption / physiology
  • Pancreas / immunology
  • Pancreas / metabolism
  • Phosphoproteins / metabolism
  • Phosphorylation
  • Signal Transduction / physiology

Substances

  • Antigens, CD
  • Blood Glucose
  • Cytokines
  • Insulin
  • Insulin Receptor Substrate Proteins
  • Intracellular Signaling Peptides and Proteins
  • Irs2 protein, mouse
  • Phosphoproteins
  • Adenosine Triphosphate
  • JNK Mitogen-Activated Protein Kinases
  • Apyrase
  • CD39 antigen