Novel and converging ways of NOX2 and SOD3 in trafficking and redox signaling in macrophages

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DOI

Macrophages and related tissue macrophage populations use the classical NADPH oxidase (NOX2) for the regulated production of superoxide and derived oxidants for pathogen combat and redox signaling. With an emphasis on macrophages, we discuss how sorting into secretory storage vesicles, agonist-responsive membrane trafficking, and segregation into sphingolipid and cholesterol-enriched microdomains (lipid rafts) determine the subcellular distribution and spatial organization of NOX2 and superoxide dismutase-3 (SOD3). We discuss how inflammatory activation of macrophages, in part through small GTPase Rab27A/B regulation of the secretory compartments, mediates the coalescence of these two proteins on the cell surface to deliver a focalized hydrogen peroxide output. In interplay with membrane-embedded oxidant transporters and redox sensitive target proteins, this arrangement allows for the autocrine and paracrine signaling, which govern macrophage activation states and transcriptional programs. By discussing examples of autocrine and paracrine redox signaling, we highlight why formation of spatiotemporal microenvironments where produced superoxide is rapidly converted to hydrogen peroxide and conveyed immediately to reach redox targets in proximal vicinity is required for efficient redox signaling. Finally, we discuss the recent discovery of macrophage-derived exosomes as vehicles of NOX2 holoenzyme export to other cells.

OriginalsprogEngelsk
Artikelnummer172
TidsskriftAntioxidants
Vol/bind10
Nummer2
Sider (fra-til)1-16
Antal sider16
ISSN2076-3921
DOI
StatusUdgivet - feb. 2021

Bibliografisk note

Funding Information:
Funding: This study was supported by the Aarhus University Graduate School (C.L.M.), the Independent Research Fund Denmark—Medical Sciences (DFF-7016-00188) (S.V.P.), the Innovation Fund Denmark (#5189-00051A) (F.V.), the Beckett Foundation (S.V.P. and F.V.), the Sofus Carl Emil Friis Foundation (F.V.), and the Aage and Johanne Louis Hansens Foundation (F.V.).

Publisher Copyright:
© 2021 by the authors.

Copyright:
Copyright 2021 Elsevier B.V., All rights reserved.

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