Therapeutic reendothelialization by induced pluripotent stem cells after vascular injury--brief report

Arterioscler Thromb Vasc Biol. 2013 Sep;33(9):2218-21. doi: 10.1161/ATVBAHA.113.301313. Epub 2013 Jul 18.

Abstract

Objective: Endothelial damage is an early requisite step for atherosclerosis after vascular injury. It has been reported that vascular wall cells can develop from induced pluripotent stem (iPS) cell-derived fetal liver kinase-1-positive (Flk-1(+)) cells. Here, we investigated the efficacies of intravenously administered iPS cell-derived Flk-1(+) cells on reendothelialization and neointimal hyperplasia in a mouse model of vascular injury.

Approach and results: Femoral arteries of KSN nude mice were injured using a steel wire. Mouse iPS cell-derived Flk-1(+) or Flk-1(-) cells were intravenously injected into those mice at 24 hours after vascular injury. Delivery of iPS cell-derived Flk-1(+) cells significantly attenuated neointimal hyperplasia compared with controls. Evans blue staining of the injured vessel revealed that administration of iPS cell-derived Flk-1(+) significantly enhanced reendothelialization compared with the Flk-1(-) cell control group. Recruitment of PKH26-labeled iPS cell-derived Flk-1(+) cells to the site of injury was also detectable. Expression level of CXCR4 in iPS cell-derived Flk-1(+) cells was 7.5-fold higher than that of iPS cell-derived Flk-1(-) cells. Stromal cell-derived factor-1α treatment significantly enhanced adhesion and migration of iPS cell-derived Flk-1(+) cells to the endothelia, but these were not observed in Flk-1(-) cells.

Conclusions: Intravenously administered iPS cell-derived Flk-1(+) cells are recruited to the site of vascular injury, thereby enhancing reendothelialization followed by suppression of neointimal hyperplasia. Administration of iPS cell-derived Flk-1(+) cells is a potentially useful therapeutic means for vascular dysfunction and prevention of restenosis after angioplasty.

Keywords: hyperplasia; induced pluripotent stem cells; vascular system injuries.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Adhesion
  • Cell Line
  • Cell Movement
  • Cell Proliferation*
  • Cell Tracking / methods
  • Chemokine CXCL12 / metabolism
  • Disease Models, Animal
  • Endothelial Cells / metabolism
  • Endothelial Cells / pathology
  • Endothelial Cells / transplantation*
  • Femoral Artery / injuries*
  • Femoral Artery / metabolism
  • Femoral Artery / pathology
  • Hyperplasia
  • Induced Pluripotent Stem Cells / metabolism
  • Induced Pluripotent Stem Cells / transplantation*
  • Injections, Intravenous
  • Luminescent Proteins / metabolism
  • Male
  • Mice
  • Mice, Nude
  • Microscopy, Fluorescence
  • Neointima
  • Receptors, CXCR4 / metabolism
  • Recombinant Proteins / metabolism
  • Red Fluorescent Protein
  • Time Factors
  • Vascular Endothelial Growth Factor Receptor-2 / metabolism
  • Vascular System Injuries / metabolism
  • Vascular System Injuries / pathology
  • Vascular System Injuries / surgery*

Substances

  • CXCR4 protein, mouse
  • Chemokine CXCL12
  • Cxcl12 protein, mouse
  • Luminescent Proteins
  • Receptors, CXCR4
  • Recombinant Proteins
  • Vascular Endothelial Growth Factor Receptor-2