| Literature DB >> 33504070 |
Tasuku Konno1, Eduardo Pinho Melo2, Joseph E Chambers3, Edward Avezov1.
Abstract
Reactive oxygen species (ROS) are produced continuously throughout the cell as products of various redox reactions. Yet these products function as important signal messengers, acting through oxidation of specific target factors. Whilst excess ROS production has the potential to induce oxidative stress, physiological roles of ROS are supported by a spatiotemporal equilibrium between ROS producers and scavengers such as antioxidative enzymes. In the endoplasmic reticulum (ER), hydrogen peroxide (H2O2), a non-radical ROS, is produced through the process of oxidative folding. Utilisation and dysregulation of H2O2, in particular that generated in the ER, affects not only cellular homeostasis but also the longevity of organisms. ROS dysregulation has been implicated in various pathologies including dementia and other neurodegenerative diseases, sanctioning a field of research that strives to better understand cell-intrinsic ROS production. Here we review the organelle-specific ROS-generating and consuming pathways, providing evidence that the ER is a major contributing source of potentially pathologic ROS.Entities:
Keywords: antioxidants; dementia; endoplasmic reticulum; hydrogen peroxide; neurodegeneration; reactive oxygen species; redox signalling
Year: 2021 PMID: 33504070 PMCID: PMC7912550 DOI: 10.3390/cells10020233
Source DB: PubMed Journal: Cells ISSN: 2073-4409 Impact factor: 6.600