Effects of Aldosterone on Chemerin Expression And Secretion in 3T3-L1 Adipocytes

Exp Clin Endocrinol Diabetes. 2018 Mar;126(3):187-193. doi: 10.1055/s-0043-118749. Epub 2017 Sep 20.

Abstract

Aldosterone plays a pivotal role in the pathogenesis of metabolic syndrome and cardiovascular disease; however, the underlying mechanisms have not been clarified. Chemerin has been characterized as an adipokine with crucial roles in obesity-associated disorders and cardiovascular homeostasis. The aim of the present study was to investigate the direct effects of aldosterone on chemerin expression and secretion in 3T3-L1 adipocytes and to identify the potential signalling pathways involved. Chemerin mRNA levels were measured using real-time PCR, whereas the levels of secreted chemerin in the culture media were determined using ELISA. Treatment with aldosterone induced time- and dose-dependent increases of chemerin gene expression and protein secretion, and effect that was mediated through the mineralocorticoid receptor. Signalling studies suggested that the NF-κB pathway is involved in aldosterone-induced chemerin expression. Taken together, our data demonstrate a direct interaction between aldosterone and chemerin in adipocytes, which may be an underlying mechanism linking aldosterone-associated metabolic abnormalities and cardiovascular disease.

MeSH terms

  • 3T3-L1 Cells / metabolism*
  • Adipocytes / metabolism*
  • Aldosterone / metabolism*
  • Animals
  • Chemokines / metabolism*
  • Intercellular Signaling Peptides and Proteins / metabolism*
  • Mice

Substances

  • Chemokines
  • Intercellular Signaling Peptides and Proteins
  • chemerin protein, mouse
  • Aldosterone