Adipocyte inflammation is essential for healthy adipose tissue expansion and remodeling

Cell Metab. 2014 Jul 1;20(1):103-18. doi: 10.1016/j.cmet.2014.05.005. Epub 2014 Jun 12.

Abstract

Chronic inflammation constitutes an important link between obesity and its pathophysiological sequelae. In contrast to the belief that inflammatory signals exert a fundamentally negative impact on metabolism, we show that proinflammatory signaling in the adipocyte is in fact required for proper adipose tissue remodeling and expansion. Three mouse models with an adipose tissue-specific reduction in proinflammatory potential were generated that display a reduced capacity for adipogenesis in vivo, while the differentiation potential is unaltered in vitro. Upon high-fat-diet exposure, the expansion of visceral adipose tissue is prominently affected. This is associated with decreased intestinal barrier function, increased hepatic steatosis, and metabolic dysfunction. An impaired local proinflammatory response in the adipocyte leads to increased ectopic lipid accumulation, glucose intolerance, and systemic inflammation. Adipose tissue inflammation is therefore an adaptive response that enables safe storage of excess nutrients and contributes to a visceral depot barrier that effectively filters gut-derived endotoxin.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipogenesis / drug effects
  • Adiponectin / metabolism
  • Adipose Tissue, White / drug effects
  • Adipose Tissue, White / metabolism*
  • Adrenergic Agonists / pharmacology
  • Animals
  • Body Weight / drug effects
  • Diet, High-Fat
  • Fatty Acid-Binding Proteins / genetics
  • Fatty Acid-Binding Proteins / metabolism
  • Fatty Liver / physiopathology
  • Female
  • Glucose Tolerance Test
  • Inflammation / metabolism*
  • Inflammation / pathology
  • Intra-Abdominal Fat / metabolism*
  • Leptin / blood
  • Lipopolysaccharides / toxicity
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Models, Animal
  • Recombinant Proteins / biosynthesis
  • Recombinant Proteins / genetics
  • Recombinant Proteins / pharmacology
  • Serum Amyloid A Protein / genetics
  • Serum Amyloid A Protein / metabolism
  • Tumor Necrosis Factor-alpha / genetics
  • Tumor Necrosis Factor-alpha / metabolism
  • Tumor Necrosis Factor-alpha / pharmacology

Substances

  • Adiponectin
  • Adrenergic Agonists
  • Fabp4 protein, mouse
  • Fatty Acid-Binding Proteins
  • Leptin
  • Lipopolysaccharides
  • Recombinant Proteins
  • Serum Amyloid A Protein
  • Tumor Necrosis Factor-alpha