Implantation of adipose-derived regenerative cells enhances ischemia-induced angiogenesis

Arterioscler Thromb Vasc Biol. 2009 Jan;29(1):61-6. doi: 10.1161/ATVBAHA.108.166496. Epub 2008 Oct 30.

Abstract

Objective: Therapeutic angiogenesis using autologous stem/progenitor cells represents a novel strategy for severe ischemic diseases. Recent reports indicated that adipose tissues could supply adipose-derived regenerative cells (ADRCs). Accordingly, we examined whether implantation of ADRCs would augment ischemia-induced angiogenesis.

Method and results: Adipose tissue was obtained from C57BL/6J mice, and ADRCs were isolated using standard methods. ADRCs expressed stromal cell-derived factor 1 (SDF-1) mRNA and proteins. Hind limb ischemia was induced and culture-expanded ADRCs, PBS, or mature adipocytes (MAs) as control cells were injected into the ischemic muscles. At 3 weeks, the ADRC group had a greater laser Doppler blood perfusion index and a higher capillary density compared to the controls. Implantation of ADRCs increased circulating endothelial progenitor cells (EPCs). SDF-1 mRNA abundance at ischemic tissues and serum SDF-1 levels were greater in the ADRC group than in the control group. Finally, intraperitoneal injection of an anti-SDF-1 neutralizing antibody reduced the number of circulating EPCs and therapeutic efficacies of ADRCs.

Conclusions: Adipose tissue would be a valuable source for cell-based therapeutic angiogenesis. Moreover, chemokine SDF-1 may play a pivotal role in the ADRCs-mediated angiogenesis at least in part by facilitating mobilization of EPCs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes / cytology
  • Adipocytes / physiology
  • Adipose Tissue / physiology
  • Adipose Tissue / transplantation*
  • Animals
  • Cell Culture Techniques
  • Cell Differentiation
  • Chemokine CXCL12 / genetics
  • Chemokine CXCL12 / physiology
  • Disease Models, Animal
  • Flow Cytometry
  • Genes, Reporter
  • Hindlimb / blood supply
  • Ischemia / complications
  • Ischemia / physiopathology*
  • Leukocytes, Mononuclear / cytology
  • Leukocytes, Mononuclear / physiology
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Neovascularization, Pathologic / physiopathology*
  • RNA, Messenger / genetics
  • Regeneration / physiology*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Vascular Endothelial Growth Factor A / genetics

Substances

  • Chemokine CXCL12
  • Cxcl12 protein, mouse
  • RNA, Messenger
  • Vascular Endothelial Growth Factor A