Oxidative Stress and Inflammation in Retinal Degeneration 2022

A special issue of Antioxidants (ISSN 2076-3921). This special issue belongs to the section "Health Outcomes of Antioxidants and Oxidative Stress".

Deadline for manuscript submissions: closed (31 May 2022) | Viewed by 3591

Special Issue Editors


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Professor of Biochemistry and Molecular Biology, Ophthalmology and Graduate Studies, Georgia Cancer Center and Culver Vision Discovery Institute, Medical College of Georgia at Augusta University, Augusta, GA, USA
Interests: retina; diabetes; diabetic retinopathy; microRNA; sickle cell retinopathy; age-related macular degeneration; retinal pigment epithelium
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Guest Editor
Department Biochemistry & Molecular Biology, The Medical College of Georgia at Augusta University, Augusta, GA 30912, USA
Interests: gut microbiome; liver diseases; aging; energy metabolism; natural compounds
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

Our previous Special Issue on “Oxidative Stress and Inflammation in Retinal Degeneration” (https://www.mdpi.com/journal/antioxidants/special_issues/oxidative_stress_retinal_degeneration), published in the 2021 volume of Antioxidants, received an overwhelming number of submissions, and was  a successful compilation of research and review articles. As this a rapidly evolving topic in the field of vision science research and much remains to be learned, we would like to further explore the role of oxidative stress and inflammation in retinal degeneration with a follow-up Special Issue for the year 2022. Robust experimental evidence points to a prominent role of inflammation and oxidative stress in the pathogenesis of many degenerative diseases of the retina (e.g., age-related macular degeneration, diabetic retinopathy, retinal vein occlusion, retinitis pigmentosa). This is supported by confirmatory studies conducted using human ocular tissues. The retina is consistently exposed to high levels of oxidative stress as a normal consequence of significant light exposure, visual signal transduction pathways that generate considerable amounts of reactive oxygen species, the oxidation of polyunsaturated fatty acids, etc. Normal healthy retinal cells do an excellent job of squelching pro-oxidant factors to maintain homeostasis. However, in aging and/or disease, the efficiency of these normal homeostatic mechanisms often declines, disrupting the balance between pro- and anti-oxidative signaling. This contributes to excessive oxidative stress, related inflammation, dysregulated immune responses, potential blood–retinal barrier compromise, and tissue damage. Thus, better understanding the mechanisms governing the cellular and molecular events that underlie the switch that precipitates the failure of the retina to respond adequately to oxidative and/or inflammatory insults, leaving the tissue susceptible to degenerative processes, may support the discovery of new therapeutic targets to prevent and treat irreversible vision loss and blindness. As such, this second Special Issue welcomes submissions of original research and review articles, commentaries, brief reports, and clinical trials related to any aspect of the role of oxidative stress and inflammation in pathogenic retinal degeneration, the identification and exploration of novel targets, and the development and testing of antioxidant and anti-inflammatory therapies.

Dr. Pamela M. Martin
Dr. Ravirajsinh N. Jadeja
Guest Editors

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Keywords

  • retinal degeneration
  • antioxidants
  • oxidative stress
  • age-related macular degeneration
  • retinal inflammation
  • therapeutic targets
  • aging retina

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Published Papers (1 paper)

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Research

13 pages, 3624 KiB  
Article
Epoxomicin, a Selective Proteasome Inhibitor, Activates AIM2 Inflammasome in Human Retinal Pigment Epithelium Cells
by Iswariyaraja Sridevi Gurubaran, Maria Hytti, Kai Kaarniranta and Anu Kauppinen
Antioxidants 2022, 11(7), 1288; https://doi.org/10.3390/antiox11071288 - 28 Jun 2022
Cited by 3 | Viewed by 2899
Abstract
Emerging evidence suggests that the intracellular clearance system plays a vital role in maintaining homeostasis and in regulating oxidative stress and inflammation in retinal pigment epithelium (RPE) cells. Dysfunctional proteasomes and autophagy in RPE cells have been associated with the pathogenesis of age-related [...] Read more.
Emerging evidence suggests that the intracellular clearance system plays a vital role in maintaining homeostasis and in regulating oxidative stress and inflammation in retinal pigment epithelium (RPE) cells. Dysfunctional proteasomes and autophagy in RPE cells have been associated with the pathogenesis of age-related macular degeneration. We have previously shown that the inhibition of proteasomes using MG-132 activates the NLR family pyrin domain containing 3 (NLRP3) inflammasome in human RPE cells. However, MG-132 is a non-selective proteasome inhibitor. In this study, we used the selective proteasome inhibitor epoxomicin to study the effect of non-functional intracellular clearance systems on inflammasome activation. Our data show that epoxomicin-induced proteasome inhibition promoted both nicotinamide adenine dinucleotide phosphate oxidase and mitochondria-mediated oxidative stress and release of mitochondrial DNA to the cytosol, which resulted in potassium efflux-dependent absence in melanoma 2 (AIM2) inflammasome activation and subsequent interleukin-1β secretion in ARPE-19 cells. The non-specific proteasome inhibitor MG-132 activated both NLRP3 and AIM2 inflammasomes and oxidative stress predominated as the activation mechanism, but modest potassium efflux was also detected. Collectively, our data suggest that a selective proteasome inhibitor is a potent inflammasome activator in human RPE cells and emphasize the role of the AIM2 inflammasome in addition to the more commonly known NLRP3 inflammasome. Full article
(This article belongs to the Special Issue Oxidative Stress and Inflammation in Retinal Degeneration 2022)
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