Free Fatty Acids Activate Renin-Angiotensin System in 3T3-L1 Adipocytes through Nuclear Factor-kappa B Pathway

J Diabetes Res. 2016:2016:1587594. doi: 10.1155/2016/1587594. Epub 2015 Dec 31.

Abstract

The activity of a local renin-angiotensin system (RAS) in the adipose tissue is closely associated with obesity-related diseases. However, the mechanism of RAS activation in adipose tissue is still unknown. In the current study, we found that palmitic acid (PA), one kind of free fatty acid, induced the activity of RAS in 3T3-L1 adipocytes. In the presence of fetuin A (Fet A), PA upregulated the expression of angiotensinogen (AGT) and angiotensin type 1 receptor (AT1R) and stimulated the secretion of angiotensin II (ANG II) in 3T3-L1 adipocytes. Moreover, the activation of RAS in 3T3-L1 adipocytes was blocked when we blocked Toll-like receptor 4 (TLR4) signaling pathway using TAK242 or NF-κB signaling pathway using BAY117082. Together, our results have identified critical molecular mechanisms linking PA/TLR4/NF-κB signaling pathway to the activity of the local renin-angiotensin system in adipose tissue.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3-L1 Cells
  • Adipocytes / drug effects*
  • Angiotensin II / metabolism
  • Angiotensinogen / analysis
  • Animals
  • Mice
  • NF-kappa B / physiology*
  • Palmitic Acid / pharmacology*
  • Receptor, Angiotensin, Type 1 / analysis
  • Renin-Angiotensin System / drug effects*
  • Renin-Angiotensin System / physiology
  • Signal Transduction*
  • Toll-Like Receptor 4 / genetics
  • Toll-Like Receptor 4 / physiology
  • alpha-2-HS-Glycoprotein / pharmacology

Substances

  • NF-kappa B
  • Receptor, Angiotensin, Type 1
  • Tlr4 protein, mouse
  • Toll-Like Receptor 4
  • alpha-2-HS-Glycoprotein
  • Angiotensinogen
  • Angiotensin II
  • Palmitic Acid