CD36 and atherosclerosis

Curr Opin Lipidol. 2000 Oct;11(5):483-91. doi: 10.1097/00041433-200010000-00006.

Abstract

CD36 has been associated with diverse normal and pathologic processes. These include scavenger receptor functions (uptake of apoptotic cells and modified lipid), lipid metabolism and fatty acid transport, adhesion, angiogenesis, modulation of inflammation, transforming growth factor-beta activation, atherosclerosis, diabetes and cardiomyopathy. Although CD36 was identified more than 25 years ago, it is only with the advent of recent genetic technology that in-vivo evidence has emerged for its physiologic and pathologic relevance. As these in-vivo studies are expanded, we will gain further insight into the mechanism(s) by which CD36 transmits a cellular signal, and this will allow the design of specific therapeutics that impact on a particular function of CD36.

Publication types

  • Review

MeSH terms

  • Animals
  • Arteriosclerosis / etiology
  • Arteriosclerosis / immunology*
  • Arteriosclerosis / metabolism
  • CD36 Antigens / chemistry
  • CD36 Antigens / genetics
  • CD36 Antigens / metabolism*
  • Cell Adhesion
  • Humans
  • Inflammation / etiology
  • Lipid Metabolism
  • Membrane Proteins*
  • Neovascularization, Pathologic
  • Receptors, Immunologic / metabolism
  • Receptors, Lipoprotein*
  • Receptors, Scavenger
  • Scavenger Receptors, Class B
  • Signal Transduction
  • Transforming Growth Factor beta / metabolism

Substances

  • CD36 Antigens
  • Membrane Proteins
  • Receptors, Immunologic
  • Receptors, Lipoprotein
  • Receptors, Scavenger
  • Scarb1 protein, mouse
  • Scavenger Receptors, Class B
  • Transforming Growth Factor beta