Cutting Edge: Slamf8 Is a Negative Regulator of Nox2 Activity in Macrophages
Author(s) -
Guoxing Wang,
Ana Clara AbadíaMolina,
Scott B. Berger,
Xavier Romero,
Michael S. O’Keeffe,
Domingo I. Rojas-Barros,
Marta Aleman,
Gongxian Liao,
Elena Maganto-García,
Manuel Fresno,
Ninghai Wang,
Cynthia Detre,
Cox Terhorst
Publication year - 2012
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.1102620
Subject(s) - nadph oxidase , receptor , escherichia coli , inflammation , enzyme , transfection , bacteria , phosphorylation , chemistry , regulator , staphylococcus aureus , phagosome , oxidase test , microbiology and biotechnology , biochemistry , biology , phagocytosis , gene , immunology , genetics
Slamf8 (CD353) is a cell surface receptor that is expressed upon activation of macrophages (MΦs) by IFN-γ or bacteria. In this article, we report that a very high NADPH oxidase (Nox2) enzyme activity was found in Slamf8(-/-) MΦs in response to Escherichia coli or Staphylococcus aureus, as well as to PMA. The elevated Nox2 activity in Slamf8(-/-) MΦs was also demonstrated in E. coli or S. aureus phagosomes by using a pH indicator system and was further confirmed by a reduction in the enzyme activity after transfection of the receptor into Slamf8-deficient primary MΦs or RAW 264.7 cells. Upon exposure to bacteria or PMA, protein kinase C activity in Slamf8(-/-) MΦs is increased. This results in an enhanced phosphorylation of p40phox, one key component of the Nox2 enzyme complex, which, in turn, leads to greater Nox2 activity. Taken together, the data show that, in response to inflammation-associated stimuli, the inducible receptor Slamf8 negatively regulates inflammatory responses.
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