Rac-dependent feedforward autoactivation of NOX2 leads to oxidative burst

• Published in: The Journal of biological chemistry Vol. 297; no. 2; p. 100982
• Main Authors: Hoang, Hanh My, Johnson, Hope Elizabeth, Heo, Jongyun
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.08.2021; American Society for Biochemistry and Molecular Biology
• Subjects: allostery; autoactivation; Cell Line; Cell Line, Tumor; Enzyme Activation; Humans; NADPH Oxidase 2 - immunology; NADPH Oxidase 2 - metabolism; NOX1; NOX2; Oxidation-Reduction; Rac; rac GTP-Binding Proteins - metabolism; Reactive Oxygen Species - metabolism; redox; Signal Transduction; superoxide; Superoxides - metabolism; dHL60; ClC-3; PMA; GEF; SOD; H2O2; redox; SITS; DIDS; Rac; GAP; autoactivation; superoxide; MAP; NOX1; allostery; NOX2
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1016/j.jbc.2021.100982

NADPH oxidase 2 (NOX2) produces the superoxide anion radical (O2−), which has functions in both cell signaling and immune defense. NOX2 is a multimeric-protein complex consisting of several protein subunits including the GTPase Rac. NOX2 uniquely facilitates an oxidative burst, which is described by initially slow O2− production, which increases over time. The NOX2 oxidative burst is considered critical to immune defense because it enables expedited O2− production in response to infections. However, the mechanism of the initiation and progression of this oxidative burst and its implications for regulation of NOX2 have not been clarified. In this study, we show that the NOX2 oxidative burst is a result of autoactivation of NOX2 coupled with the redox function of Rac. NOX2 autoactivation begins when active Rac triggers NOX2 activation and the subsequent production of O2−, which in turn activates redox-sensitive Rac. This activated Rac further activates NOX2, amplifying the feedforward cycle and resulting in a NOX2-mediated oxidative burst. Using mutagenesis-based kinetic and cell analyses, we show that enzymatic activation of Rac is exclusively responsible for production of the active Rac trigger that initiates NOX2 autoactivation, whereas redox-mediated Rac activation is the main driving force of NOX2 autoactivation and contributes to generation of ∼98% of the active NOX2 in cells. The results of this study provide insight into the regulation of NOX2 function, which could be used to develop therapeutics to control immune responses associated with dysregulated NOX2 oxidative bursts.