Electrophilic fatty acids regulate matrix metalloproteinase activity and expression

J Biol Chem. 2011 May 6;286(18):16074-81. doi: 10.1074/jbc.M111.225029. Epub 2011 Mar 15.

Abstract

Nitro-fatty acids (NO(2)-FA) are electrophilic signaling mediators formed by reactions of nitric oxide and nitrite. NO(2)-FA exert anti-inflammatory signaling actions through post-translational protein modifications. We report that nitro-oleic acid (OA-NO(2)) stimulates proMMP-7 and proMMP-9 proteolytic activity via adduction of the conserved cysteine switch domain thiolate. Biotin-labeled OA-NO(2) showed this adduction occurs preferentially with latent forms of MMP, confirming a role for thiol alkylation by OA-NO(2) in MMP activation. In addition to regulating pro-MMP activation, MMP expression was modulated by OA-NO(2) via activation of peroxisome proliferator-activated receptor-γ. MMP-9 transcription was decreased in phorbol 12-myristate 13-acetate-stimulated THP-1 macrophages to an extent similar to that induced by the peroxisome proliferator-activated receptor-γ agonist Rosiglitazone. This was affirmed using a murine model of atherosclerosis, ApoE(-/-) mice, where in vivo OA-NO(2) administration suppressed MMP expression in atherosclerotic lesions. These findings reveal that electrophilic fatty acid derivatives can serve as effectors during inflammation, first by activating pro-MMP proteolytic activity via alkylation of the cysteine switch domain, and then by transcriptionally inhibiting MMP expression, thereby limiting the further progression of inflammatory processes.

Publication types

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

MeSH terms

  • Animals
  • Carcinogens / pharmacology
  • Cell Line
  • Enzyme Activation / drug effects
  • Enzyme Precursors / biosynthesis*
  • Enzyme Precursors / genetics
  • Gene Expression Regulation, Enzymologic*
  • Humans
  • Hypoglycemic Agents / pharmacology
  • Inflammation / enzymology
  • Inflammation / genetics
  • Inflammation / pathology
  • Matrix Metalloproteinase 9 / biosynthesis*
  • Matrix Metalloproteinase 9 / genetics
  • Metalloendopeptidases / biosynthesis*
  • Metalloendopeptidases / genetics
  • Mice
  • Mice, Knockout
  • Oleic Acids / metabolism
  • Oleic Acids / pharmacology*
  • PPAR gamma / antagonists & inhibitors
  • PPAR gamma / genetics
  • PPAR gamma / metabolism
  • Protein Structure, Tertiary
  • Rosiglitazone
  • Tetradecanoylphorbol Acetate / pharmacology
  • Thiazolidinediones / pharmacology
  • Transcription, Genetic / drug effects
  • Transcription, Genetic / genetics

Substances

  • Carcinogens
  • Enzyme Precursors
  • Hypoglycemic Agents
  • Oleic Acids
  • PPAR gamma
  • Thiazolidinediones
  • Rosiglitazone
  • Metalloendopeptidases
  • pro-matrix metalloproteinase 9
  • promatrilysin
  • Matrix Metalloproteinase 9
  • Tetradecanoylphorbol Acetate