CD36 signaling in vascular redox stress

Free Radic Biol Med. 2019 May 20:136:159-171. doi: 10.1016/j.freeradbiomed.2019.02.021. Epub 2019 Feb 27.

Abstract

Scavenger receptor CD36 is a multifunctional membrane protein that promotes thrombosis in conditions of oxidative stress such as metabolic disorders including dyslipidemia, diabetes mellitus, and chronic inflammation. In these conditions, specific reactive oxidant species are generated that are context and cell dependent. In the vasculature, CD36 signaling in smooth muscle cells and endothelial cells promotes generation of reactive oxygen species, genetic downregulation of antioxidant genes, and impaired smooth muscle and endothelial function. In hematopoietic cells, CD36 signaling enhances platelet dysfunction thus decreasing the threshold for platelet activation and accelerating arterial thrombosis, whereas in macrophages, CD36 promotes lipid-laden foam cell formation and atherosclerosis. These clinically significant processes are mediated through complex redox regulated signaling mechanisms that include Src-family kinases, MAP kinases and other downstream effectors. We provide an overview of CD36 signaling in vascular redox stress highlighting the role in oxidant generation in vascular and hematopoietic cells, but with special emphasis on platelets and dyslipidemia.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Blood Platelets / metabolism
  • CD36 Antigens / metabolism*
  • Dyslipidemias / metabolism
  • Endothelial Cells / metabolism
  • Humans
  • Oxidation-Reduction
  • Oxidative Stress / physiology*
  • Platelet Activation / physiology
  • Signal Transduction / physiology*

Substances

  • CD36 Antigens