Journal of Vascular Surgery
Volume 45, Issue 6, Supplement , Pages A48-A56, June 2007

The chemokine system in arteriogenesis and hind limb ischemia

  • Paula K. Shireman, MD

      Affiliations

    • Corresponding Author InformationReprint requests: Paula K. Shireman, MD, Associate Professor, Division of Vascular Surgery, MC 7741, 7703 Floyd Curl Dr, San Antonio, TX 78229-3900.

South Texas Veterans Health Care System, Departments of Surgery and Medicine, Sam and Ann Barshop Institute for Longevity and Aging Studies, the University of Texas Health Science Center, San Antonio, Tex.

Received 21 December 2006; accepted 11 February 2007.

Chemokines (chemotactic cytokines) are important in the recruitment of leukocytes to injured tissues and, as such, play a pivotal role in arteriogenesis and the tissue response to ischemia. Hind limb ischemia represents a complex model with arteriogenesis (collateral artery formation) occurring in tissues with normal perfusion while areas exhibiting ischemic necrosis undergo angiogenesis and skeletal muscle regeneration; monocytes and macrophages play an important role in all three of these processes. In addition to leukocyte trafficking, chemokines are produced by and chemokine receptors are present on diverse cell types, including myoblasts, endothelial, and smooth muscle cells. Thus, the chemokine system may have direct effects as well as inflammatory-mediated effects on arteriogenesis, angiogenesis, and skeletal muscle regeneration. This article reviews the complexity of the hind limb ischemia model and the role of the chemokine system in arteriogenesis and the tissue response to ischemia. Special emphasis will be placed on the roles of monocytes/macrophages and CCL2/monocyte chemotactic protein-1 (MCP-1) in these processes.

 

 Competition of interest: none.Supported by grants from the National Institutes of Health (HL070158, HL074236) and the Veterans Administration.

PII: S0741-5214(07)00316-3

doi:10.1016/j.jvs.2007.02.030

Journal of Vascular Surgery
Volume 45, Issue 6, Supplement , Pages A48-A56, June 2007