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Peroxisomal Hydrogen Peroxide Metabolism and Signaling in Health and Disease

Hydrogen peroxide (H(2)O(2)), a non-radical reactive oxygen species generated during many (patho)physiological conditions, is currently universally recognized as an important mediator of redox-regulated processes. Depending on its spatiotemporal accumulation profile, this molecule may act as a signa...

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Detalles Bibliográficos
Autores principales: Lismont, Celien, Revenco, Iulia, Fransen, Marc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6695606/
https://www.ncbi.nlm.nih.gov/pubmed/31357514
http://dx.doi.org/10.3390/ijms20153673
Descripción
Sumario:Hydrogen peroxide (H(2)O(2)), a non-radical reactive oxygen species generated during many (patho)physiological conditions, is currently universally recognized as an important mediator of redox-regulated processes. Depending on its spatiotemporal accumulation profile, this molecule may act as a signaling messenger or cause oxidative damage. The focus of this review is to comprehensively evaluate the evidence that peroxisomes, organelles best known for their role in cellular lipid metabolism, also serve as hubs in the H(2)O(2) signaling network. We first briefly introduce the basic concepts of how H(2)O(2) can drive cellular signaling events. Next, we outline the peroxisomal enzyme systems involved in H(2)O(2) metabolism in mammals and reflect on how this oxidant can permeate across the organellar membrane. In addition, we provide an up-to-date overview of molecular targets and biological processes that can be affected by changes in peroxisomal H(2)O(2) metabolism. Where possible, emphasis is placed on the molecular mechanisms and factors involved. From the data presented, it is clear that there are still numerous gaps in our knowledge. Therefore, gaining more insight into how peroxisomes are integrated in the cellular H(2)O(2) signaling network is of key importance to unravel the precise role of peroxisomal H(2)O(2) production and scavenging in normal and pathological conditions.