Macrophages in obesity are characterised by increased IL-1β response to calcium-sensing receptor signals

Int J Obes (Lond). 2022 Oct;46(10):1883-1891. doi: 10.1038/s41366-022-01135-x. Epub 2022 Aug 5.

Abstract

Objective: Obesity is complicated by inflammatory activation of the innate immune system. Stimulation of the calcium-sensing receptor (CaSR) by extra-cellular calcium ions ([Ca2+]ex) can trigger NLRP3 inflammasome activation and inflammation. We hypothesised, that this mechanism might contribute to the activation of adipose tissue (AT) in obesity, and investigated [Ca2+]ex-induced, CaSR mediated IL-1β release by macrophages in obesity.

Methods: [Ca2+]ex-induced IL-1β release was investigated in monocyte-derived macrophages (MDM) generated from peripheral blood of patients with obesity and from normal-weight controls. Visceral and subcutaneous AT biosamples were stimulated with [Ca2+]ex, and IL-1β release, as well as expression of NLRP3 inflammasome and cytokine genes, was determined.

Results: Both MDM and AT readily responded with concentration-dependent IL-1β release already at low, near physiological concentrations to addition of [Ca2+]ex, which was more than 80 fold higher than the LPS-induced effect. IL-1β levels induced by [Ca2+]ex were significantly higher not only in MDM from patients with obesity compared to controls, but also in visceral versus subcutaneous AT. This fat-depot difference was also reflected by mRNA expression levels of inflammasome and cytokine genes.

Conclusions: Obesity renders macrophages more susceptible to [Ca2+]ex-induced IL-1β release and pyroptosis. Increased susceptibility was independent of the response to LPS and circulating CRP arguing against mere pro-inflammatory pre-activation of monocytes. Instead, we propose that CaSR mediated signalling is relevant for the deleterious innate immune activation in obesity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Calcium / metabolism
  • Humans
  • Inflammasomes* / metabolism
  • Interleukin-1beta / metabolism
  • Lipopolysaccharides / metabolism
  • Macrophages / metabolism
  • NLR Family, Pyrin Domain-Containing 3 Protein* / metabolism
  • Obesity / metabolism
  • RNA, Messenger / metabolism
  • Receptors, Calcium-Sensing / metabolism

Substances

  • IL1B protein, human
  • Inflammasomes
  • Interleukin-1beta
  • Lipopolysaccharides
  • NLR Family, Pyrin Domain-Containing 3 Protein
  • RNA, Messenger
  • Receptors, Calcium-Sensing
  • Calcium