Vitamin D signalling in adipose tissue

Br J Nutr. 2012 Dec 14;108(11):1915-23. doi: 10.1017/S0007114512003285. Epub 2012 Oct 9.

Abstract

Vitamin D deficiency and the rapid increase in the prevalence of obesity are both considered important public health issues. The classical role of vitamin D is in Ca homoeostasis and bone metabolism. Growing evidence suggests that the vitamin D system has a range of physiological functions, with vitamin D deficiency contributing to the pathogenesis of several major diseases, including obesity and the metabolic syndrome. Clinical studies have shown that obese individuals tend to have a low vitamin D status, which may link to the dysregulation of white adipose tissue. Recent studies suggest that adipose tissue may be a direct target of vitamin D. The expression of both the vitamin D receptor and 25-hydroxyvitamin D 1α-hydroxylase (CYP27B1) genes has been shown in murine and human adipocytes. There is evidence that vitamin D affects body fat mass by inhibiting adipogenic transcription factors and lipid accumulation during adipocyte differentiation. Some recent studies demonstrate that vitamin D metabolites also influence adipokine production and the inflammatory response in adipose tissue. Therefore, vitamin D deficiency may compromise the normal metabolic functioning of adipose tissue. Given the importance of the tissue in energy balance, lipid metabolism and inflammation in obesity, understanding the mechanisms of vitamin D action in adipocytes may have a significant impact on the maintenance of metabolic health. In the present review, we focus on the signalling role of vitamin D in adipocytes, particularly the potential mechanisms through which vitamin D may influence adipose tissue development and function.

Publication types

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

MeSH terms

  • Adipogenesis*
  • Adipokines / metabolism
  • Adipose Tissue / immunology
  • Adipose Tissue / metabolism*
  • Animals
  • Humans
  • Insulin Resistance
  • Lipid Metabolism*
  • Obesity / etiology
  • Obesity / immunology
  • Obesity / metabolism
  • Receptors, Calcitriol / metabolism*
  • Signal Transduction*
  • Vitamin D / metabolism*
  • Vitamin D Deficiency / immunology
  • Vitamin D Deficiency / metabolism
  • Vitamin D Deficiency / physiopathology

Substances

  • Adipokines
  • Receptors, Calcitriol
  • Vitamin D