Hyperhomocysteinemia suppresses bone marrow CD34+/VEGF receptor 2+ cells and inhibits progenitor cell mobilization and homing to injured vasculature-a role of β1-integrin in progenitor cell migration and adhesion

FASEB J. 2015 Jul;29(7):3085-99. doi: 10.1096/fj.14-267989. Epub 2015 Apr 8.

Abstract

Hyperhomocysteinemia (HHcy) impairs re-endothelialization and accelerates vascular remodeling. The role of CD34(+)/VEGF receptor (VEGFR) 2(+) progenitor cells (PCs) in vascular repair in HHcy is unknown. We studied the effect of HHcy on PCs and its role in vascular repair in severe HHcy (∼150 μM), which was induced in cystathionine-β synthase heterozygous mice fed a high-methionine diet for 8 weeks. Vascular injury was introduced by carotid air-dry endothelium denudation. CD34(+)/VEGFR2(+) cells were examined by flow cytometry. HHcy reduced bone marrow (BM) CD34(+)/VEGFR2(+) cells and suppressed replenishment of postinjury CD34(+)/VEGFR2(+) cells in peripheral blood (PB). Donor green fluorescent protein-positive PC homing to the injured vessel was reduced in HHcy after CD34(+) PCs from enhanced green fluorescent protein mice were adoptively transferred following carotid injury. CD34(+) PC transfusion partially reversed HHcy-suppressed re-endothelialization and HHcy-induced neointimal formation. Furthermore, homocysteine (Hcy) inhibited proliferation, adhesion, and migration and suppressed β1-integrin expression and activity in human CD34(+) endothelial colony-forming cells (ECFCs) isolated from PBs in a dose-dependent manner. A functional-activating β1-integrin antibody rescued Hcy-suppressed adhesion and migration in CD34(+) ECFCs. In conclusion, HHcy reduces BM CD34(+)/VEGFR2(+) generation and suppresses CD34(+)/VEGFR2(+) cell mobilization and homing to the injured vessel via β1-integrin inhibition, which partially contributes to impaired re-endothelialization and vascular remodeling.

Keywords: cell therapy; endothelial repair; vascular remodeling.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Antigens, CD34 / metabolism
  • Bone Marrow Cells / pathology*
  • Bone Marrow Cells / physiology*
  • Carotid Artery Injuries / pathology
  • Carotid Artery Injuries / physiopathology
  • Cell Adhesion
  • Cell Movement
  • Colony-Forming Units Assay
  • Cystathionine beta-Synthase / deficiency
  • Cystathionine beta-Synthase / genetics
  • Cystathionine beta-Synthase / metabolism
  • Disease Models, Animal
  • Green Fluorescent Proteins / genetics
  • Hematopoietic Stem Cell Transplantation
  • Hematopoietic Stem Cells / pathology
  • Hematopoietic Stem Cells / physiology
  • Humans
  • Hyperhomocysteinemia / genetics
  • Hyperhomocysteinemia / pathology*
  • Hyperhomocysteinemia / physiopathology*
  • Integrin beta1 / physiology*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Neointima / pathology
  • Neointima / physiopathology
  • Neointima / prevention & control
  • Vascular Endothelial Growth Factor Receptor-2 / metabolism*
  • Vascular Remodeling

Substances

  • Antigens, CD34
  • Integrin beta1
  • enhanced green fluorescent protein
  • Green Fluorescent Proteins
  • KDR protein, human
  • Kdr protein, mouse
  • Vascular Endothelial Growth Factor Receptor-2
  • Cystathionine beta-Synthase