CCL2-CCR2 signaling axis in obesity and metabolic diseases

J Cell Physiol. 2024 Apr;239(4):e31192. doi: 10.1002/jcp.31192. Epub 2024 Jan 29.

Abstract

Obesity and metabolic diseases, such as insulin resistance, type 2 diabetes, nonalcoholic fatty liver disease, and cardiovascular ailments, represent formidable global health challenges, bearing considerable implications for both morbidity and mortality rates. It has become increasingly evident that chronic, low-grade inflammation plays a pivotal role in the genesis and advancement of these conditions. The involvement of C-C chemokine ligand 2 (CCL2) and its corresponding receptor, C-C chemokine receptor 2 (CCR2), has been extensively documented in numerous inflammatory maladies. Recent evidence indicates that the CCL2/CCR2 pathway extends beyond immune cell recruitment and inflammation, exerting a notable influence on the genesis and progression of metabolic syndrome. The present review seeks to furnish a comprehensive exposition of the CCL2-CCR2 signaling axis within the context of obesity and metabolic disorders, elucidating its molecular mechanisms, functional roles, and therapeutic implications.

Keywords: CCL2; CCR2; adipose tissue; inflammation; metabolic syndrome.

Publication types

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

MeSH terms

  • Animals
  • Chemokine CCL2 / metabolism
  • Humans
  • Inflammation
  • Ligands
  • Metabolic Diseases* / metabolism
  • Mice
  • Obesity* / metabolism
  • Receptors, CCR2* / metabolism
  • Signal Transduction

Substances

  • Chemokine CCL2
  • Ligands
  • Receptors, CCR2
  • CCL2 protein, human
  • CCR2 protein, human