Atypical Chemokine Receptors in Cardiovascular Disease

Thromb Haemost. 2019 Apr;119(4):534-541. doi: 10.1055/s-0038-1676988. Epub 2019 Feb 4.

Abstract

Inflammation has been well recognized as one of the main drivers of atherosclerosis development and therefore cardiovascular diseases (CVDs). It has been shown that several chemokines, small 8 to 12 kDa cytokines with chemotactic properties, play a crucial role in the pathophysiology of atherosclerosis. Chemokines classically mediate their effects by binding to G-protein-coupled receptors called chemokine receptors. In addition, chemokines can also bind to atypical chemokine receptors (ACKRs). ACKRs fail to induce G-protein-dependent signalling pathways and thus subsequent cellular response, but instead are able to internalize, scavenge or transport chemokines. In this review, we will give an overview of the current knowledge about the involvement of ACKR1-4 in CVDs and especially in atherosclerosis development. In the recent years, several studies have highlighted the importance of ACKRs in CVDs, although there are still several controversies and unexplored aspects that have to be further elucidated. A better understanding of the precise role of these atypical receptors may pave the way towards novel and improved therapeutic strategies.

Publication types

  • Review

MeSH terms

  • Animals
  • Atherosclerosis / metabolism*
  • Cardiovascular Diseases / metabolism*
  • Chemokines / metabolism
  • Chemotaxis
  • Cytokines / metabolism
  • Duffy Blood-Group System / metabolism
  • Humans
  • Inflammation
  • Lipids / chemistry
  • Receptors, CCR / metabolism
  • Receptors, CXCR / metabolism
  • Receptors, Cell Surface / metabolism
  • Receptors, Chemokine / metabolism*
  • Shear Strength
  • Signal Transduction
  • Stress, Mechanical

Substances

  • ACKR1 protein, human
  • ACKR2 protein, human
  • ACKR3 protein, human
  • ACKR4 protein, human
  • Chemokines
  • Cytokines
  • Duffy Blood-Group System
  • Lipids
  • Receptors, CCR
  • Receptors, CXCR
  • Receptors, Cell Surface
  • Receptors, Chemokine