Genetic lineage tracing analysis of c-kit+ stem/progenitor cells revealed a contribution to vascular injury-induced neointimal lesions

J Mol Cell Cardiol. 2018 Aug:121:277-286. doi: 10.1016/j.yjmcc.2018.07.252. Epub 2018 Jul 24.

Abstract

Aims: Accumulating evidence indicates the presence of vascular stem/progenitor cells that may play a role in endothelial repair and lesion formation in the injured artery, in which c-kit+ stem/progenitor cells have been reported to differentiate into endothelial and smooth muscle cells in vitro and in ischemic tissue. In this study, we investigated whether and how endogenous c-kit+ stem/progenitor cells contribute to vascular injury and neointima formation in vivo.

Methods and results: We created Kit-CreERxRosa26-RFP mice and performed genetic lineage tracing analysis of c-kit+ stem/progenitor cells in injury-induced neointima formation in vivo. We provide direct evidence that endogenous c-kit+ stem/progenitor cells minimally differentiate into endothelial or smooth muscle cells facilitating vascular repair, but predominantly generate monocytes/macrophages and granulocytes contributing to vascular immuno-inflammatory response to endothelial injury. Although c-kit+ cells reside in both bone marrow and vessel wall, bone marrow transplantation data indicate that bone marrow-derived c-kit+ cells are the main source for enhancing neointima formation. Furthermore, treatment of ACK2, a c-kit receptor antagonizer, attenuates neointimal hyperplasia after injury at least in part by depleting c-kit+ cells and their generated progeny.

Conclusions: c-kit+ stem/progenitor cells are not a main source for endothelial regeneration and smooth muscle accumulation of the large artery injury, but a plausible interventional approach to reduce vascular immuno-inflammatory response and subsequently to ameliorate vascular lesions.

Keywords: C-kit(+) progenitor; Cell lineage tracing; Endothelial cell; Myeloid cell; Neointma formation; Smooth muscle cell.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arteries / growth & development*
  • Arteries / injuries
  • Cell Differentiation / genetics
  • Cell Line
  • Cell Lineage / genetics*
  • Cell Movement / genetics
  • Endothelial Cells / metabolism
  • Endothelial Cells / pathology
  • Granulocytes / metabolism
  • Humans
  • Macrophages / metabolism
  • Mice
  • Monocytes / metabolism
  • Neointima / genetics
  • Neointima / pathology
  • Proto-Oncogene Proteins c-kit / genetics*
  • Stem Cells / cytology*
  • Stem Cells / metabolism
  • Tunica Intima / growth & development*
  • Tunica Intima / injuries
  • Tunica Intima / pathology

Substances

  • Proto-Oncogene Proteins c-kit