Endotoxin conditioning induces VCP/p97-mediated and inducible nitric-oxide synthase-dependent Tyr284 nitration in protein phosphatase 2A

J Biol Chem. 2010 Mar 19;285(12):8711-8. doi: 10.1074/jbc.M109.099788. Epub 2010 Jan 25.

Abstract

Endotoxins activate Toll-like receptors and reprogram cells to be refractory to secondary exposure. Here we found that activation of different Toll-like receptors elicited a time- and dose-dependent increase in the levels of the protein phosphatase 2A catalytic subunit (PP2Ac) but not its partner A subunit. We purified the lipopolysaccharide-induced form of PP2A by chromatography plus immunoprecipitation and used mass spectrometry to identify VCP/p97 as a novel partner for PP2Ac. Endogenous VCP/p97 and PP2Ac were co-immunoprecipitated from primary murine macrophages and human lymphocytes. GST-VCP/p97 bound purified PP2A in pulldown assays, showing direct protein-protein interaction. Endotoxin conditioning of macrophages induced formation of 3-nitrotyrosine in the PP2Ac associated with VCP/p97, a response severely reduced in macrophages from iNOS knock-out mice. The reaction of purified PP2A with peroxynitrite dissociated the A subunit, and 3-nitro-Tyr(284) was identified in PP2Ac by mass spectrometry. Myc-PP2Ac (Y284F) expressed in cells was resistant to peroxynitrite-induced nitration and reduction of A subunit binding. Transient expression of either VCP/p97 or PP2Ac was sufficient to elevate levels of the dual specificity phosphatase DUSP1, reduce p38 MAPK activation, and suppress tumor necrosis factor-alpha release. We propose that VCP/p97-mediated Tyr nitration of PP2A increases the levels of phosphatases PP2A and DUSP1 to contribute to the refractory response of conditioned cells.

Publication types

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

MeSH terms

  • Adenosine Triphosphatases / chemistry*
  • Adenosine Triphosphatases / metabolism*
  • Animals
  • Cell Cycle Proteins / chemistry*
  • Cell Cycle Proteins / metabolism*
  • Dual Specificity Phosphatase 1 / metabolism
  • Endotoxins / metabolism*
  • Humans
  • Lymphocytes / metabolism
  • Macrophages / metabolism
  • Mice
  • Mice, Knockout
  • Nitric Oxide Synthase Type II / metabolism*
  • Nitrogen / chemistry
  • Protein Interaction Mapping
  • Protein Phosphatase 2 / chemistry*
  • Tyrosine / chemistry*
  • Valosin Containing Protein

Substances

  • Cell Cycle Proteins
  • Endotoxins
  • Tyrosine
  • Nitric Oxide Synthase Type II
  • Protein Phosphatase 2
  • DUSP1 protein, human
  • Dual Specificity Phosphatase 1
  • Dusp1 protein, mouse
  • Adenosine Triphosphatases
  • VCP protein, human
  • Valosin Containing Protein
  • Vcp protein, mouse
  • Nitrogen