Angiogenesis

, Volume 13, Issue 3, pp 219–226

MCP-1 promotes mural cell recruitment during angiogenesis in the aortic ring model

  • Alfred C. Aplin
  • Eric Fogel
  • Roberto F. Nicosia
Original Paper

DOI: 10.1007/s10456-010-9179-8

Cite this article as:
Aplin, A.C., Fogel, E. & Nicosia, R.F. Angiogenesis (2010) 13: 219. doi:10.1007/s10456-010-9179-8

Abstract

Rings of rat or mouse aorta embedded in collagen gels produce angiogenic outgrowths in response to the injury of the dissection procedure. Aortic outgrowths are composed of branching endothelial tubes and surrounding mural cells. Mural cells emerge following endothelial sprouting and gradually increase during the maturation of the neovessels. Treatment of aortic cultures with angiopoietin-1 (Ang-1), an angiogenic factor implicated in vascular maturation and remodeling, stimulates the mural cell recruitment process. Ang-1 induces expression of many cytokines and chemokines including monocyte chemotactic protein-1 (MCP-1). Inhibition of p38 MAP kinase, a signaling molecule required for mural cell recruitment, blocks Ang1-induced MCP-1 expression. Recombinant MCP-1 dose-dependently increases mural cell number while an anti-MCP-1 blocking antibody reduces it. In addition, antibody mediated neutralization of MCP-1 abrogates the stimulatory effect of Ang-1 on mural cell recruitment. Aortic rings from genetically modified mice deficient in MCP-1 or its receptor CCR2 have fewer mural cells than controls. MCP-1 deficiency also impairs the mural cell recruitment activity of Ang-1. Our studies indicate that spontaneous and Ang1-induced mural cell recruitment in the aortic ring of model of angiogenesis are in part mediated by MCP-1. These results implicate MCP-1 as one of the mediators of mural cell recruitment in the aortic ring model, and suggest that chemokine pathways may contribute to the assembly of the vessel wall during the angiogenesis response to injury.

Keywords

ChemokinesCollagenNeovascularizationPericytes

Abbreviations

Ang-1

Angiopoietin-1

bFGF

Basic fibroblast growth factor

EBM

Endothelial basal medium

HB-EGF

Heparin binding-endothelial growth factor

HGF

Hepatocyte growth factor

MCP-1

Monocyte chemotactic protein-1

VEGF

Vascular endothelial growth factor

Copyright information

© Springer Science+Business Media B.V. 2010

Authors and Affiliations

  • Alfred C. Aplin
    • 1
  • Eric Fogel
    • 2
  • Roberto F. Nicosia
    • 1
    • 2
  1. 1.Department of PathologyUniversity of WashingtonSeattleUSA
  2. 2.Division of Pathology and Laboratory Medicine (S-113)Veterans Administration Puget Sound Health Care SystemSeattleUSA