Vascular Stem/Progenitor Cell Migration and Differentiation in Atherosclerosis

Antioxid Redox Signal. 2018 Jul 10;29(2):219-235. doi: 10.1089/ars.2017.7171. Epub 2017 Jul 5.

Abstract

Significance: Atherosclerosis is a major cause for the death of human beings, and it takes place in large- and middle-sized arteries. The pathogenesis of the disease has been widely investigated, and new findings on vascular stem/progenitor cells could have an impact on vascular regeneration. Recent Advances: Recent studies have shown that abundant stem/progenitor cells present in the vessel wall are mainly responsible for cell accumulation in the intima during vascular remodeling. It has been demonstrated that the mobilization and recruitment of tissue-resident stem/progenitor cells give rise to endothelial and smooth muscle cells (SMCs) that participate in vascular repair and remodeling such as neointimal hyperplasia and arteriosclerosis. Interestingly, cell lineage tracing studies indicate that a large proportion of SMCs in neointimal lesions is derived from adventitial stem/progenitor cells.

Critical issues: The influence of stem/progenitor cell behavior on the development of atherosclerosis is crucial. An understanding of the regulatory mechanisms that control stem/progenitor cell migration and differentiation is essential for stem/progenitor cell therapy for vascular diseases and regenerative medicine.

Future directions: Identification of the detailed process driving the migration and differentiation of vascular stem/progenitor cells during the development of atherosclerosis, discovery of the environmental cues, and signaling pathways that control cell fate within the vasculature will facilitate the development of new preventive and therapeutic strategies to combat atherosclerosis. Antioxid. Redox Signal. 00, 000-000.

Keywords: atherosclerosis; migration; progenitor cells; stem cells.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Adult
  • Animals
  • Atherosclerosis / etiology*
  • Blood Vessels / cytology*
  • Calcinosis / etiology
  • Cell Differentiation*
  • Cell Movement*
  • Chemokines / metabolism
  • Endothelium, Vascular / physiology
  • Humans
  • Macrophages / cytology
  • Mice
  • Muscle, Smooth, Vascular / cytology
  • Neointima / etiology
  • Reactive Oxygen Species / metabolism
  • Stem Cells / cytology
  • Stem Cells / metabolism
  • Stem Cells / physiology*

Substances

  • Chemokines
  • Reactive Oxygen Species