Extracellular Matrix Metalloproteinase Inducer EMMPRIN (CD147) in Cardiovascular Disease

Int J Mol Sci. 2018 Feb 8;19(2):507. doi: 10.3390/ijms19020507.

Abstract

The receptor EMMPRIN is involved in the development and progression of cardiovascular diseases and in the pathogenesis of myocardial infarction. There are several binding partners of EMMPRIN mediating the effects of EMMPRIN in cardiovascular diseases. EMMPRIN interaction with most binding partners leads to disease progression by mediating cytokine or chemokine release, the activation of platelets and monocytes, as well as the formation of monocyte-platelet aggregates (MPAs). EMMPRIN is also involved in atherosclerosis by mediating the infiltration of pro-inflammatory cells. There is also evidence that EMMPRIN controls energy metabolism of cells and that EMMPRIN binding partners modulate intracellular glycosylation and trafficking of EMMPRIN towards the cell membrane. In this review, we systematically discuss these multifaceted roles of EMMPRIN and its interaction partners, such as Cyclophilins, in cardiovascular disease.

Keywords: cardiovascular disease; immunoglobulin superfamily; inflammation; monocyte-platelet aggregates; platelets.

Publication types

  • Review

MeSH terms

  • Animals
  • Basigin / chemistry
  • Basigin / genetics*
  • Basigin / metabolism*
  • Blood Platelets / metabolism
  • Cardiovascular Diseases / etiology*
  • Cardiovascular Diseases / metabolism*
  • Carrier Proteins / metabolism
  • Cell Adhesion
  • Cell Communication
  • Cell Movement
  • Extracellular Matrix / metabolism
  • Humans
  • Inflammation / etiology
  • Inflammation / metabolism
  • Monocytes / metabolism
  • Platelet Aggregation
  • Protein Binding
  • Protein Interaction Domains and Motifs

Substances

  • Carrier Proteins
  • Basigin