期刊
ANTIOXIDANTS
卷 12, 期 2, 页码 -出版社
MDPI
DOI: 10.3390/antiox12020429
关键词
NOX2; oxidative stress; inflammation; immunity; therapeutics
Nicotinamide adenine dinucleotide phosphate (NADPH) oxidase (NOX) is an enzyme complex that generates superoxide or hydrogen peroxide (H2O2) and plays a crucial role in various biological functions. Among its isoforms, NOX2 is widely expressed in different cell types and is involved in regulating immunity and pathologies associated with oxidative stress and inflammation. Modulating NOX2 activity is an important therapeutic strategy to reduce damage caused by its hyperactivation. This review analyzes the mechanisms of NOX2 activation and regulation, its role in innate immunity, pathologies associated with its hyperactivation, and the latest inhibitory strategies.
Nicotinamide adenine dinucleotide phosphate (NADPH) oxidase (NOX) is a multisubunit enzyme complex that participates in the generation of superoxide or hydrogen peroxide (H2O2) and plays a key role in several biological functions. Among seven known NOX isoforms, NOX2 was the first identified in phagocytes but is also expressed in several other cell types including endothelial cells, platelets, microglia, neurons, and muscle cells. NOX2 has been assigned multiple roles in regulating many aspects of innate and adaptive immunity, and human and mouse models of NOX2 genetic deletion highlighted this key role. On the other side, NOX2 hyperactivation is involved in the pathogenesis of several diseases with different etiologies but all are characterized by an increase in oxidative stress and inflammatory process. From this point of view, the modulation of NOX2 represents an important therapeutic strategy aimed at reducing the damage associated with its hyperactivation. Although pharmacological strategies to selectively modulate NOX2 are implemented thanks to new biotechnologies, this field of research remains to be explored. Therefore, in this review, we analyzed the role of NOX2 at the crossroads between immunity and pathologies mediated by its hyperactivation. We described (1) the mechanisms of activation and regulation, (2) human, mouse, and cellular models studied to understand the role of NOX2 as an enzyme of innate immunity, (3) some of the pathologies associated with its hyperactivation, and (4) the inhibitory strategies, with reference to the most recent discoveries.
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