Interleukin-33/ST2 system attenuates aldosterone-induced adipogenesis and inflammation

Mol Cell Endocrinol. 2015 Aug 15:411:20-7. doi: 10.1016/j.mce.2015.04.007. Epub 2015 Apr 17.

Abstract

Interleukin-33 (IL-33) but not soluble ST2 (sST2) exerts anti-inflammatory and protective effects in several tissues. Aldosterone, a proinflammatory mediator which promotes adipogenesis, is elevated in obese patients. The aim of this study was to investigate the interactions between IL-33/ST2 system and Aldosterone in adipose tissue. Rats fed a high fat diet presented increased sST2 expression, diminished IL-33/sST2 ratio and enhanced levels of differentiation and inflammation in adipose tissue as compared to controls. A similar pattern was observed in adipose tissue from C57BL/6 Aldosterone-treated mice. In both animal models, Aldosterone was correlated with sST2. Treatment of 3T3-L1 adipocytes with IL-33 delayed adipocyte differentiation diminished lipid accumulation and decreased inflammation. Aldosterone decreased IL-33 and increased sST2 expressions in differentiated adipocytes. Aldosterone-induced adipocyte differentiation and inflammation were blocked by IL-33 treatment, but sST2 did not exert any effects. The crosstalk between IL-33/ST2 and Aldosterone could be relevant in the metabolic consequences of obesity.

Keywords: Adipocyte differentiation; Adipose tissue; Aldosterone; IL-33/ST2 system.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3-L1 Cells
  • Adipogenesis / drug effects
  • Adipogenesis / physiology*
  • Adipose Tissue / drug effects
  • Adipose Tissue / metabolism*
  • Aldosterone / pharmacology*
  • Animals
  • Diet, High-Fat
  • Inflammation / metabolism
  • Interleukin-1 Receptor-Like 1 Protein
  • Interleukin-33 / metabolism*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Obesity / metabolism
  • Rats
  • Rats, Wistar
  • Receptors, Interleukin / metabolism*

Substances

  • Il1rl1 protein, mouse
  • Interleukin-1 Receptor-Like 1 Protein
  • Interleukin-33
  • Receptors, Interleukin
  • Aldosterone