Brief communicationExtracellular superoxide dismutase in vessels and airways of humans and baboons
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2020, Journal of Stroke and Cerebrovascular DiseasesCitation Excerpt :As such, the SODs participate in a range of critical homeostatic and disease-related processes, including cardiovascular development and the tissue response to ischemic injury.25–27 SOD3 is particularly unique in that it is expressed predominantly in the lung, kidney, and vasculature, where it mitigates free radical damage by initiating the conversion of oxygen radicals to lesser intermediates.28 Studies indicate that the R213G SOD3 polymorphism, which results in reduced tissue retention through altered c-terminal processing, is associated with premature aging in mice and a doubling of cardiovascular risk in humans.29,30
The dynamic uptake and release of SOD3 from intracellular stores in macrophages modulates the inflammatory response
2019, Redox BiologyCitation Excerpt :Transcription of the SOD3 gene is epigenetically regulated by both methylation of the promotor region as well as by histone acetylation/deacetylation controlling gene accessibility [21–25]. These elements are likely to explain the finding that SOD3 protein can be detected in only a limited amount of cell types including pulmonary fibroblasts and epithelial cells as well as vascular smooth muscle cells [26–30]. Indeed, the lack of SOD3 expression in human pulmonary artery endothelial cells has been shown to rely on epigenetic regulation, as the expression could be induced by demethylation of the promotor region as well as modulation of histone acetylation [22,31].
Extracellular superoxide dismutase (SOD3): An antioxidant or prooxidant in the extracellular space?
2019, Oxidative Stress: Eustress and Distress