Obesity-associated proinflammatory cytokines increase calcium sensing receptor (CaSR) protein expression in primary human adipocytes and LS14 human adipose cell line

Arch Biochem Biophys. 2010 Aug 15;500(2):151-6. doi: 10.1016/j.abb.2010.05.033. Epub 2010 Jun 4.

Abstract

Obesity-associated health complications are thought to be in part due to the low-grade proinflammatory state that characterizes this disease. The calcium sensing receptor (CaSR), which is expressed in human adipose cells, plays an important role in diseases involving inflammation. To assess the relevance of this protein in adipose pathophysiology, we evaluated its expression in adipocytes under obesity-related proinflammatory conditions. As in primary adipose cells, we established that LS14, a recently described human adipose cell line, expresses the CaSR. Differentiated LS14 and primary adipose cells were exposed overnight to cytokines typically involved in obesity-related inflammation (interleukin (IL)1beta, IL6 and tumor necrosis factor (TNF)alpha). The cytokines increased CaSR abundance in differentiated adipocytes. We incubated LS14 cells with medium previously conditioned (CM) by adipose tissue from subjects with a wide range of body mass index (BMI). Cells exposed to CM from subjects of higher BMI underwent a greater increase in CaSR protein, likely resulting from the greater proinflammatory cytokines secreted from obese tissue. Our observations that proinflammatory factors increase CaSR levels in adipocytes, and the reported ability of CaSR to elevate cytokine levels, open new aspects in the study of obesity inflammatory state pathophysiology, providing a potential novel therapeutic prevention and treatment target.

MeSH terms

  • Adipocytes / cytology
  • Adipocytes / drug effects
  • Adipocytes / metabolism*
  • Adipose Tissue / metabolism
  • Cell Differentiation
  • Cell Line
  • Cells, Cultured
  • Culture Media, Conditioned
  • Cytokines / metabolism*
  • Cytokines / pharmacology
  • Humans
  • Inflammation Mediators / metabolism*
  • Inflammation Mediators / pharmacology
  • Interleukin-1beta / pharmacology
  • Interleukin-6 / pharmacology
  • NF-kappa B / metabolism
  • Obesity / metabolism*
  • Receptors, Calcium-Sensing / metabolism*
  • Tumor Necrosis Factor-alpha / pharmacology

Substances

  • CASR protein, human
  • Culture Media, Conditioned
  • Cytokines
  • IL6 protein, human
  • Inflammation Mediators
  • Interleukin-1beta
  • Interleukin-6
  • NF-kappa B
  • Receptors, Calcium-Sensing
  • Tumor Necrosis Factor-alpha