Topical HDL administration reduces vein graft atherosclerosis in apo E deficient mice

Atherosclerosis. 2011 Feb;214(2):271-8. doi: 10.1016/j.atherosclerosis.2010.09.024. Epub 2010 Sep 29.

Abstract

Objective: Use of autologous vein grafts for surgical revascularisation is limited by vein graft failure. Topical high-density lipoprotein (HDL) administration on the adventitial side of vein grafts was evaluated as a new therapeutic modality to improve vein graft patency and function.

Methods: Caval veins of C57BL/6 apo E(-/-) mice were grafted to the right carotid arteries of recipient 3 month-old C57BL/6 TIE2-LacZ/apo E(-/-) mice. HDL (200 μg/ml; 50 μl) in 20% pluronic F-127 gel was applied on the adventitial side of vein grafts.

Results: Topical HDL application reduced intimal area by 55% (p < 0.001) at day 28 compared to control mice. Blood flow quantified by micro magnetic resonance imaging at day 28 was 2.8-fold (p < 0.0001) higher in grafts of topical HDL treated mice than in control mice. Topical HDL potently reduced intimal inflammation and resulted in enhanced endothelial regeneration as evidenced by a 1.9-fold (p < 0.05) increase in the number of CD31 positive endothelial cells. HDL potently enhanced migration and adhesion of endothelial colony-forming cells (ECFCs) in vitro, and these effects were dependent on signaling via scavenger receptor-BI, extracellular signal-regulated kinases, and NO, and on increased β1 integrin expression. Correspondingly, the number of CD31 β-galactosidase double positive cells, reflecting incorporated circulating progenitor cells, was 3.9-fold (p < 0.01) higher in grafts of HDL treated mice than in control grafts.

Conclusions: Topical HDL administration on the adventitial side of vein grafts attenuates vein graft atherosclerosis via increased incorporation of circulating progenitor cells in the endothelium, enhanced endothelial regeneration, and reduced intimal inflammation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Topical
  • Animals
  • Apolipoprotein A-I / genetics
  • Apolipoprotein A-I / metabolism
  • Apolipoproteins E / deficiency*
  • Apolipoproteins E / genetics
  • Atherosclerosis / etiology
  • Atherosclerosis / genetics
  • Atherosclerosis / metabolism
  • Atherosclerosis / pathology
  • Atherosclerosis / physiopathology
  • Atherosclerosis / prevention & control*
  • Carotid Arteries / surgery
  • Chemotaxis, Leukocyte / drug effects
  • Disease Models, Animal
  • Endothelial Cells / drug effects
  • Endothelial Cells / metabolism
  • Extracellular Signal-Regulated MAP Kinases / metabolism
  • Gene Transfer Techniques
  • Graft Occlusion, Vascular / etiology
  • Graft Occlusion, Vascular / genetics
  • Graft Occlusion, Vascular / metabolism
  • Graft Occlusion, Vascular / pathology
  • Graft Occlusion, Vascular / physiopathology
  • Graft Occlusion, Vascular / prevention & control*
  • Integrin beta1 / metabolism
  • Lipoproteins, HDL / administration & dosage*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Nitric Oxide / metabolism
  • Phosphorylation
  • Regional Blood Flow / drug effects
  • Signal Transduction / drug effects
  • Stem Cells / drug effects
  • Stem Cells / metabolism
  • Time Factors
  • Vascular Endothelial Growth Factor A / metabolism
  • Vascular Grafting / adverse effects*
  • Vascular Patency / drug effects
  • Venae Cavae / drug effects*
  • Venae Cavae / pathology
  • Venae Cavae / physiopathology
  • Venae Cavae / transplantation*

Substances

  • APOA1 protein, human
  • Apolipoprotein A-I
  • Apolipoproteins E
  • Integrin beta1
  • Lipoproteins, HDL
  • Vascular Endothelial Growth Factor A
  • vascular endothelial growth factor A, mouse
  • Nitric Oxide
  • Extracellular Signal-Regulated MAP Kinases