Critical roles of cold shock domain protein A as an endogenous angiogenesis inhibitor in skeletal muscle

Antioxid Redox Signal. 2011 Oct 15;15(8):2109-20. doi: 10.1089/ars.2010.3714. Epub 2011 Jun 14.

Abstract

Angiogenesis is regulated by the local balance between angiogenic stimulators and inhibitors and is maintained by muscle-derived angiogenic factors in ischemic tissues.

Aims: Our objectives were to investigate the effect of cold shock domain protein A (CSDA) as an endogenous angiogenesis inhibitor and to develop a novel strategy of therapeutic angiogenesis by blocking CSDA expression.

Results: In human skeletal muscle cells, CSDA was upregulated during hypoxia when cells were damaged and apoptosis was induced. CSDA expression could repress the activity of hypoxia inducible factor-1α and nuclear factor κB, because CSDA can competitively bind the hypoxia response element and the nuclear factor κB-binding element. As a result, vascular endothelial growth factor-A, interleukin-6, and interleukin-8 secretions from skeletal muscle cells were decreased. Further, CSDA depletion increased the secretion level of these angiogenic factors. In a hindlimb ischemia model, transfer of short-hairpin RNA targeting CSDA ameliorated ischemia without direct transfer of angiogenic factors. In this ischemic tissue, vascular endothelial growth factor-A, interleukin-6, and CXCL2 protein levels were increased.

Innovation and conclusion: CSDA appears to play a critical role as an endogenous angiogenesis inhibitor in skeletal muscle, and RNA interference targeting of CSDA is a promising gene therapy strategy for treating peripheral arterial disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Angiogenesis Inhibitors / genetics
  • Angiogenesis Inhibitors / metabolism*
  • Animals
  • Apoptosis / genetics
  • Apoptosis / physiology
  • Blotting, Western
  • CCAAT-Enhancer-Binding Proteins / genetics
  • CCAAT-Enhancer-Binding Proteins / metabolism*
  • Cells, Cultured
  • Chemokine CXCL2 / metabolism
  • Electrophoretic Mobility Shift Assay
  • Fluorescent Antibody Technique
  • Heat-Shock Proteins / genetics
  • Heat-Shock Proteins / metabolism*
  • Hindlimb / pathology
  • Humans
  • Immunoenzyme Techniques
  • Interleukin-6 / metabolism
  • Interleukin-8 / metabolism
  • Ischemia / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Muscle, Skeletal / metabolism*
  • Muscle, Skeletal / pathology
  • Necrosis
  • Real-Time Polymerase Chain Reaction
  • Vascular Endothelial Growth Factor A / metabolism

Substances

  • Angiogenesis Inhibitors
  • CCAAT-Enhancer-Binding Proteins
  • Chemokine CXCL2
  • Heat-Shock Proteins
  • Interleukin-6
  • Interleukin-8
  • Vascular Endothelial Growth Factor A
  • YBX3 protein, human