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PI(3)P‐p40 phox binding regulates NADPH oxidase activation in mouse macrophages and magnitude of inflammatory responses in vivo
Author(s) -
Bagaitkar Juhi,
Barbu Emilia A.,
PerezZapata Lizet J.,
Austin Anthony,
Huang Guangming,
Pallat Sabine,
Dinauer Mary C.
Publication year - 2017
Publication title -
journal of leukocyte biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.819
H-Index - 191
eISSN - 1938-3673
pISSN - 0741-5400
DOI - 10.1189/jlb.3ab0316-139r
Subject(s) - nadph oxidase , superoxide , chronic granulomatous disease , inflammation , biology , zymosan , reactive oxygen species , oxidase test , p22phox , chemokine , microbiology and biotechnology , biochemistry , immunology , enzyme , in vitro
Mutations in the leukocyte NADPH oxidase that abrogate superoxide production result in chronic granulomatous disease (CGD), an inherited immunodeficiency associated with recurrent infections and inflammatory complications. The cytosolic regulatory subunit p40 phox plays a specialized role in stimulating NADPH oxidase activity on intracellular membranes via its phosphatidylinositol 3‐phosphate [PI(3)P]‐binding domain, as revealed by studies largely focused on neutrophils. Whether PI(3)P‐p40 phox ‐regulated superoxide production contributes to regulating inflammatory responses is not well understood. Here, we report that mice expressing p40 phox R58A, which lacks PI(3)P binding, had impaired macrophage NADPH oxidase activity and increased sterile inflammation. p40 phoxR58A/R58A macrophages exhibited diminished phagosome reactive oxygen species (ROS) in response to certain particulate and soluble ligands, including IgG‐opsonized particles and a TLR2 agonist, along with unexpected defects in plasma membrane oxidase activity. Compared with wild‐type (WT) mice, p40 phoxR58A/R58A mice had elevated numbers of newly recruited neutrophils and monocytes in peritoneal inflammation elicited by zymosan, monosodium urate (MSU) crystals, or sodium periodate. At later time points, higher numbers of inflammatory macrophages in p40 phoxR58A/R58A mice were consistent with delayed resolution. Our studies demonstrate a critical role of PI(3)P‐p40 phox binding for optimal activation of the NADPH oxidase in macrophages. Furthermore, selective loss of PI(3)P‐regulated NADPH oxidase activity was sufficient to enhance significantly responses to inflammation and delay resolution.