Adiponectin stimulates angiogenesis in response to tissue ischemia through stimulation of amp-activated protein kinase signaling

J Biol Chem. 2004 Jul 2;279(27):28670-4. doi: 10.1074/jbc.M402558200. Epub 2004 Apr 28.

Abstract

Obesity is a risk factor for the development of cardiovascular diseases that are associated with impaired angiogenesis. Adiponectin is an adipocyte-specific adipocytokine with anti-atherogenic and anti-diabetic properties, and its plasma levels are reduced in association with obesity-linked diseases. Here, we investigated whether adiponectin regulates angiogenesis in response to tissue ischemia using adiponectin knock-out (KO) mice. Angiogenic repair of ischemic hind limbs was impaired in adiponectin-KO mice compared with wild-type (WT) mice as evaluated by laser Doppler flow method and capillary density analyses. Adenovirus-mediated supplement of adiponectin accelerated angiogenic repair in both adiponectin-KO and WT mice. Intramuscular injection of an adenovirus encoding dominant-negative AMP-activated kinase diminished the improvement in limb perfusion seen in WT mice and abolished the adiponectin-induced enhancement of perfusion. These data indicate that adiponectin can function to stimulate angiogenesis in response to ischemic stress by promoting AMP-activated kinase signaling. Therefore, adiponectin may be useful in the treatment for obesity-related vascular deficiency diseases.

Publication types

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

MeSH terms

  • AMP-Activated Protein Kinases
  • Adenoviridae / genetics
  • Adipocytes / metabolism
  • Adiponectin
  • Animals
  • Antibodies, Monoclonal / metabolism
  • Blotting, Western
  • Capillaries / metabolism
  • Gene Transfer Techniques
  • Genes, Dominant
  • Intercellular Signaling Peptides and Proteins*
  • Ischemia*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Multienzyme Complexes / metabolism*
  • Neovascularization, Pathologic*
  • Obesity
  • Platelet Endothelial Cell Adhesion Molecule-1 / biosynthesis
  • Protein Serine-Threonine Kinases / metabolism*
  • Proteins / genetics
  • Proteins / metabolism*
  • Signal Transduction
  • Time Factors

Substances

  • Adiponectin
  • Antibodies, Monoclonal
  • Intercellular Signaling Peptides and Proteins
  • Multienzyme Complexes
  • Platelet Endothelial Cell Adhesion Molecule-1
  • Proteins
  • Protein Serine-Threonine Kinases
  • AMP-Activated Protein Kinases