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Intracellular Sources of ROS/H2O2 in Health and Neurodegeneration: Spotlight on Endoplasmic Reticulum

Journal

CELLS
Volume 10, Issue 2, Pages -

Publisher

MDPI
DOI: 10.3390/cells10020233

Keywords

reactive oxygen species; hydrogen peroxide; endoplasmic reticulum; redox signalling; antioxidants; neurodegeneration; dementia

Categories

Funding

  1. UK Dementia Research Institute from the Medical Research Council
  2. Alzheimer's Research
  3. Alzheimer's Society UK
  4. Portuguese national funds, FCT-Foundation for Science and Technology through operational programs CRESC Algarve 2020 and COMPETE 2020 [EMBRC.PT ALG-01-0145-FEDER-022121]
  5. MRC-MRC [MCMB MR/R009120/1]
  6. Grifols ALTA training award
  7. MRC [UKDRI-2004] Funding Source: UKRI

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Reactive oxygen species (ROS) are continuously produced in cells as important signal messengers, but excess production can lead to oxidative stress. The endoplasmic reticulum is a major source of potentially pathologic ROS.
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.

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