PI3Kγ controls oxidative bursts in neutrophils via interactions with PKCα and p47phox
Author(s) -
Katja Lehmann,
Jörg P. Müller,
Bernhard Schlott,
Philipp Skroblin,
Dagmar Barz,
Johannes Norgauer,
Reinhard Wetzker
Publication year - 2008
Publication title -
biochemical journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.706
H-Index - 265
eISSN - 1470-8728
pISSN - 0264-6021
DOI - 10.1042/bj20081268
Subject(s) - nadph oxidase , protein kinase c , reactive oxygen species , pi3k/akt/mtor pathway , microbiology and biotechnology , intracellular , chemistry , respiratory burst , kinase , innate immune system , biochemistry , signal transduction , biology , receptor
Neutrophils release reactive oxygen species (ROS) as part of the innate inflammatory immune response. Phosphoinositide 3-kinase gamma (PI3Kgamma), which is induced by the bacterial peptide N-formylmethionyl-leucyl-phenylalanine (fMLP), has been identified as an essential intracellular mediator of ROS production. However, the complex signalling reactions that link PI3Kgamma with ROS synthesis by NADPH oxidase have not yet been described in detail. We found that activation of neutrophils by fMLP triggers the association of PI3Kgamma with protein kinase Calpha (PKCalpha). Specific inhibition of PI3Kgamma suppresses fMLP-mediated activation of PKCalpha activity and ROS production, suggesting that the protein kinase activity of PI3Kgamma is involved. Our data suggest that the direct interaction of PI3Kgamma with PKCalpha forms a discrete regulatory module of fMLP-dependent ROS production in neutrophils.
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