Stanniocalcin-1 suppresses superoxide generation in macrophages through induction of mitochondrial UCP2

J Leukoc Biol. 2009 Oct;86(4):981-8. doi: 10.1189/jlb.0708454. Epub 2009 Jul 14.

Abstract

Mammalian STC1 decreases the mobility of macrophages and diminishes their response to chemokines. In the current experiments, we sought to determine the impact of STC1 on energy metabolism and superoxide generation in mouse macrophages. STC1 decreases ATP level in macrophages but does not affect the activity of respiratory chain complexes I-IV. STC1 induces the expression of mitochondrial UCP2, diminishing mitochondrial membrane potential and superoxide generation; studies in UCP2 null and gp91phox null macrophages suggest that suppression of superoxide by STC1 is UCP2-dependent yet is gp91phox-independent. Furthermore, STC1 blunts the effects of LPS on superoxide generation in macrophages. Exogenous STC1 is internalized by macrophages within 10 min and localizes to the mitochondria, suggesting a role for circulating and/or tissue-derived STC1 in regulating macrophage function. STC1 induces arrest of the cell cycle at the G1 phase and reduces cell necrosis and apoptosis in serum-starved macrophages. Our data identify STC1 as a key regulator of superoxide generation in macrophages and suggest that STC1 may profoundly affect the immune/inflammatory response.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adenosine Triphosphate / genetics
  • Adenosine Triphosphate / immunology
  • Animals
  • Apoptosis / genetics
  • Apoptosis / immunology
  • Cell Line
  • Cell Movement / genetics
  • Cell Movement / immunology
  • Electron Transport / immunology
  • G1 Phase / genetics
  • G1 Phase / immunology
  • Gene Expression Regulation / genetics
  • Gene Expression Regulation / immunology
  • Glycoproteins / genetics
  • Glycoproteins / immunology*
  • Ion Channels / genetics
  • Ion Channels / immunology*
  • Macrophages, Peritoneal / immunology*
  • Macrophages, Peritoneal / pathology
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / immunology*
  • Mice
  • Mice, Knockout
  • Mitochondria / genetics
  • Mitochondria / immunology*
  • Mitochondrial Proteins / genetics
  • Mitochondrial Proteins / immunology*
  • NADPH Oxidase 2
  • NADPH Oxidases / genetics
  • NADPH Oxidases / immunology*
  • Necrosis / genetics
  • Necrosis / immunology
  • Protein Transport / genetics
  • Protein Transport / immunology
  • Superoxides / immunology*
  • Time Factors
  • Uncoupling Protein 2

Substances

  • Glycoproteins
  • Ion Channels
  • Membrane Glycoproteins
  • Mitochondrial Proteins
  • Ucp2 protein, mouse
  • Uncoupling Protein 2
  • Superoxides
  • teleocalcin
  • Adenosine Triphosphate
  • Cybb protein, mouse
  • NADPH Oxidase 2
  • NADPH Oxidases