Arachidonic acid-dependent activation of a p22(phox)-based NAD(P)H oxidase mediates angiotensin II-induced mesangial cell protein synthesis and fibronectin expression via Akt/PKB

Antioxid Redox Signal. 2006 Sep-Oct;8(9-10):1497-508. doi: 10.1089/ars.2006.8.1497.

Abstract

Angiotensin II (Ang II) induces protein synthesis and hypertrophy through arachidonic acid (AA)- and redoxdependent activation of the serine-threonine kinase Akt/PKB in mesangial cells (MCs). The role of NAD(P)H oxidase component p22( phox ) was explored in this signaling pathway and in Ang II-induced expression of the extracellular matrix protein fibronectin. Ang II causes activation of Akt/PKB and induces fibronectin protein expression, effects abrogated by phospholipase A(2) inhibition and mimicked by AA. Ang II and AAalso elicited an increase in fibronectin expression that was reduced with a dominant negative mutant of Akt/PKB. Exposure of the cells to hydrogen peroxide stimulates Akt/PKB activity and fibronectin synthesis. The antioxidant N-acetylcysteine abolished Ang II- and AA-induced Akt/PKB activation and fibronectin expression. Western blot analysis revealed high levels of p22( phox ) in MCs. Antisense (AS) but not sense oligonucleotides for p22( phox ) prevented ROS generation in response to Ang II and AA. AS p22( phox ) inhibited Ang II- or AA-induced Akt/PKB as well as protein synthesis and fibronectin expression. These data provide the first evidence, in MCs, of activation by AAof a p22( phox )-based NAD(P)H oxidase and subsequent generation of ROS. Moreover, this pathway mediates the effect of Ang II on Akt/PKB-induced protein synthesis and fibronectin expression.

Publication types

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

MeSH terms

  • Acetylcysteine / pharmacology
  • Angiotensin II / pharmacology*
  • Animals
  • Arachidonic Acid / pharmacology*
  • Cells, Cultured
  • Enzyme Inhibitors / pharmacology
  • Fibronectins / genetics
  • Fibronectins / metabolism*
  • Hydrogen Peroxide / pharmacology
  • Mesangial Cells / cytology
  • Mesangial Cells / drug effects
  • Mesangial Cells / metabolism*
  • Microscopy, Fluorescence
  • Mutation / genetics
  • NADPH Oxidases / physiology*
  • Oligonucleotides, Antisense / genetics
  • Oxidation-Reduction
  • Phospholipases A / antagonists & inhibitors
  • Phosphorylation / drug effects
  • Protein Biosynthesis / drug effects*
  • Proto-Oncogene Proteins c-akt / genetics
  • Proto-Oncogene Proteins c-akt / metabolism*
  • Rats
  • Reactive Oxygen Species / metabolism

Substances

  • Enzyme Inhibitors
  • Fibronectins
  • Oligonucleotides, Antisense
  • Reactive Oxygen Species
  • Angiotensin II
  • Arachidonic Acid
  • Hydrogen Peroxide
  • NADPH Oxidases
  • Cyba protein, rat
  • Proto-Oncogene Proteins c-akt
  • Phospholipases A
  • Acetylcysteine