Regulation by fatty acids of angiotensinogen gene expression in preadipose cells

Biochem J. 1997 Feb 15;322 ( Pt 1)(Pt 1):235-9. doi: 10.1042/bj3220235.

Abstract

Adipocytes represent an important source of angiotensiongen (AT). Angiotensin II (A-II) stimulates in vitro and in vivo the formation and release of prostacyclin which acts as a potent adipogenic signal in triggering the terminal differentiation of preadipocytes into adipocytes [Darimont, Vassaux, Gaillard. Ailhaud and Négrel (1994) Int. J. Obes. 18, 783-788]. Since fatty acids have been reported to activate in preadipose cells the expression of various differentiation-dependent genes, the role of fatty acids in the regulation of AT gene expression was investigated. Long-chain natural and non-metabolized fatty acids as well as peroxisome proliferators behave as activators of AT gene expression. Accumulation of AT mRNA parallels that of the adipocyte fatty acid-binding protein gene and is primarily due to transcriptional activation of the AT gene. AT mRNA decreases after fatty acid removal (half-life approx. 8 h). Secretion of AT is also observed but appears mainly as a late differentiation-dependent phenomenon. Thus the AT gene appears to be a fatty acid-responsive gene; this regulation provides a potential link between the flux of fatty acids and the potential of adipose tissue to produce AT and possibly A-II.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes / cytology
  • Adipocytes / metabolism*
  • Angiotensinogen / biosynthesis
  • Angiotensinogen / genetics*
  • Angiotensinogen / metabolism
  • Animals
  • Carrier Proteins / biosynthesis
  • Carrier Proteins / drug effects
  • Carrier Proteins / genetics
  • Cell Differentiation
  • Cell Line
  • Fatty Acid-Binding Protein 7
  • Fatty Acid-Binding Proteins
  • Fatty Acids / physiology*
  • Gene Expression Regulation / drug effects*
  • Half-Life
  • Intracellular Signaling Peptides and Proteins
  • Mice
  • Myelin P2 Protein / biosynthesis
  • Myelin P2 Protein / drug effects
  • Neoplasm Proteins*
  • Nerve Tissue Proteins*
  • RNA, Messenger / biosynthesis
  • RNA, Messenger / metabolism
  • Stem Cells / cytology
  • Stem Cells / drug effects
  • Stem Cells / metabolism*
  • Transcription, Genetic

Substances

  • Carrier Proteins
  • Fabp5 protein, mouse
  • Fabp7 protein, mouse
  • Fabp7 protein, rat
  • Fatty Acid-Binding Protein 7
  • Fatty Acid-Binding Proteins
  • Fatty Acids
  • Intracellular Signaling Peptides and Proteins
  • Myelin P2 Protein
  • Neoplasm Proteins
  • Nerve Tissue Proteins
  • RNA, Messenger
  • peroxisome proliferator-binding protein, rat
  • Angiotensinogen