Nox, Nox, Are You There? the Role of NADPH Oxidases in the Peripheral Nervous System
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Mary Ann Liebert Inc.
Abstract
Significance: Reactive oxygen species (ROS) contribute to multiple aspects of peripheral nervous system (PNS) biology ranging from physiological processes (e.g., axonal outgrowth and regeneration) to pathophysiology (e.g., nerve degeneration). Although ROS are derived from multiple sources, NADPH oxidase (Nox) family members are dedicated to ROS generation. Noxs are expressed in the PNS, and their overexpression is associated with detrimental effects on nerve function and contributes, at least in part, to peripheral neuropathies. Recent Advances: Of the seven members, studies mostly focused on Nox1, Nox2, and Nox4, which are expressed in the PNS in a cell-specific manner. We have also recently identified human Nox5 in sural nerve biopsies. When maintained at homeostatic levels, Noxs regulate several aspects of peripheral nerve health, most notably neurite outgrowth and axonal regeneration following nerve lesion. While Nox2 and Nox4 dysregulation is a major source of oxidative stress in PNS disorders, including neuropathic pain and diabetic peripheral neuropathy, recent evidence also implicates Nox1 and Nox5. Critical Issues: Although there is compelling evidence for a direct role of Noxs on nerve function, little is known about their subcellular localization, intercellular regulation, and interaction. These, together with redox signaling, are considered crucial components of nerve redox status. In addition, the lack of isoform-specific inhibitors limits conclusions about the physiological role of Noxs in the PNS and their therapeutic potential in peripheral neuropathies. Future Directions: Future research using isoform-specific genetic and pharmacological approaches are therefore needed to better understand the significance of Nox enzymes in PNS (patho) physiology. Antioxid. Redox Signal. 37, 613-630. © Copyright 2022, Mary Ann Liebert, Inc., publishers 2022.
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Nadph oxidases (nox), Neuron, Neuropathy, Peripheral nervous system (pns), Reactive oxygen species, Schwann cells, Humans, Nadph oxidase 1, Nadph oxidase 4, Nadph oxidases, Oxidative stress, Peripheral nervous system, Peripheral nervous system diseases, Reactive oxygen metabolite, Reduced nicotinamide adenine dinucleotide phosphate oxidase, Reduced nicotinamide adenine dinucleotide phosphate oxidase 1, Reduced nicotinamide adenine dinucleotide phosphate oxidase 4, Blood pressure regulation, Carboxy terminal sequence, Cell differentiation, Cell membrane, Cell metabolism, Cell nucleus membrane, Cell respiration, Cellular distribution, Chemotherapy-induced peripheral neuropathy, Chronic inflammatory demyelinating polyneuropathy, Cognition, Conformational transition, Defense mechanism, Diabetic neuropathy, Endoplasmic reticulum, Enzyme activation, Enzyme active site, Extracellular space, Gene deletion, Gene overexpression, Growth cone, High throughput screening, Host resistance, Human, Innate immunity, Intercellular signaling, Nerve biopsy, Nerve cell, Nerve conduction velocity, Nerve fiber regeneration, Nerve function, Nerve regeneration, Neurite outgrowth, Neuropathic pain, Oxidation reduction reaction, Oxidative phosphorylation, Pathogen clearance, Peripheral nerve, Physiological process, Protein function, Redox signaling, Respiratory chain, Review, Schwann cell, Signal transduction, Skin biopsy, Spinal ganglion, Structural homology, Sural nerve, Tissue repair, Vascular smooth muscle, Genetics, Metabolism, Peripheral neuropathy