Hypoxia increases serum amyloid A3 (SAA3) in differentiated 3T3-L1 adipocytes

Inflammation. 2013 Oct;36(5):1107-10. doi: 10.1007/s10753-013-9644-9.

Abstract

Hypoxia has been implicated as a possible cause of adipose tissue inflammation. Furthermore, the acute phase protein serum amyloid A (SAA) has been associated with the modulation of the adipogenic process, and it is well-known that obese individuals have increased levels of SAA. The effect of hypoxia in the expression and production of SAA was examined in murine 3T3-L1 adipocytes. Hypoxia leads to a substantial increase in SAA3 mRNA and protein level, apparently in a time-dependent manner (threefold in 48 h), in fully differentiated 3T3-L1, followed by reestablishment of gene expression to basal levels after 24 h of reoxygenation. Hypoxia-induced SAA may be one of the key molecules to the development of the inflammatory response in adipose tissue.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3 Cells
  • Adipocytes / metabolism*
  • Adipose Tissue / metabolism*
  • Animals
  • Cell Differentiation
  • Cell Hypoxia
  • Cell Line
  • Cell Survival
  • Inflammation / metabolism
  • Mice
  • Obesity / metabolism
  • RNA, Messenger / biosynthesis
  • Serum Amyloid A Protein / biosynthesis
  • Serum Amyloid A Protein / genetics
  • Serum Amyloid A Protein / metabolism*

Substances

  • RNA, Messenger
  • Saa3 protein, mouse
  • Serum Amyloid A Protein