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Contribution of NRF2 to sulfur metabolism and mitochondrial activity

NF-E2-related factor 2 (NRF2) plays a crucial role in the maintenance of cellular homeostasis by regulating various enzymes and proteins that are involved in the redox reactions utilizing sulfur. While substantial impacts of NRF2 on mitochondrial activity have been described, the precise mechanism b...

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Autores principales: Alam, Md Morshedul, Kishino, Akihiro, Sung, Eunkyu, Sekine, Hiroki, Abe, Takaaki, Murakami, Shohei, Akaike, Takaaki, Motohashi, Hozumi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9941419/
https://www.ncbi.nlm.nih.gov/pubmed/36758466
http://dx.doi.org/10.1016/j.redox.2023.102624
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author Alam, Md Morshedul
Kishino, Akihiro
Sung, Eunkyu
Sekine, Hiroki
Abe, Takaaki
Murakami, Shohei
Akaike, Takaaki
Motohashi, Hozumi
author_facet Alam, Md Morshedul
Kishino, Akihiro
Sung, Eunkyu
Sekine, Hiroki
Abe, Takaaki
Murakami, Shohei
Akaike, Takaaki
Motohashi, Hozumi
author_sort Alam, Md Morshedul
collection PubMed
description NF-E2-related factor 2 (NRF2) plays a crucial role in the maintenance of cellular homeostasis by regulating various enzymes and proteins that are involved in the redox reactions utilizing sulfur. While substantial impacts of NRF2 on mitochondrial activity have been described, the precise mechanism by which NRF2 regulates mitochondrial function is still not fully understood. Here, we demonstrated that NRF2 increased intracellular persulfides by upregulating the cystine transporter xCT encoded by Slc7a11, a well-known NRF2 target gene. Persulfides have been shown to play an important role in mitochondrial function. Supplementation with glutathione trisulfide (GSSSG), which is a form of persulfide, elevated the mitochondrial membrane potential (MMP), increased the oxygen consumption rate (OCR) and promoted ATP production. Persulfide-mediated mitochondrial activation was shown to require the mitochondrial sulfur oxidation pathway, especially sulfide quinone oxidoreductase (SQOR). Consistently, NRF2-mediated mitochondrial activation was also dependent on SQOR activity. This study clarified that the facilitation of persulfide production and sulfur metabolism in mitochondria by increasing cysteine availability is one of the mechanisms for NRF2-dependent mitochondrial activation.
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spelling pubmed-99414192023-02-22 Contribution of NRF2 to sulfur metabolism and mitochondrial activity Alam, Md Morshedul Kishino, Akihiro Sung, Eunkyu Sekine, Hiroki Abe, Takaaki Murakami, Shohei Akaike, Takaaki Motohashi, Hozumi Redox Biol Articles from the Special Issue on Recent advances in sulfur biology and chemistry, Edited by: Dr. Peter Nagy NF-E2-related factor 2 (NRF2) plays a crucial role in the maintenance of cellular homeostasis by regulating various enzymes and proteins that are involved in the redox reactions utilizing sulfur. While substantial impacts of NRF2 on mitochondrial activity have been described, the precise mechanism by which NRF2 regulates mitochondrial function is still not fully understood. Here, we demonstrated that NRF2 increased intracellular persulfides by upregulating the cystine transporter xCT encoded by Slc7a11, a well-known NRF2 target gene. Persulfides have been shown to play an important role in mitochondrial function. Supplementation with glutathione trisulfide (GSSSG), which is a form of persulfide, elevated the mitochondrial membrane potential (MMP), increased the oxygen consumption rate (OCR) and promoted ATP production. Persulfide-mediated mitochondrial activation was shown to require the mitochondrial sulfur oxidation pathway, especially sulfide quinone oxidoreductase (SQOR). Consistently, NRF2-mediated mitochondrial activation was also dependent on SQOR activity. This study clarified that the facilitation of persulfide production and sulfur metabolism in mitochondria by increasing cysteine availability is one of the mechanisms for NRF2-dependent mitochondrial activation. Elsevier 2023-02-02 /pmc/articles/PMC9941419/ /pubmed/36758466 http://dx.doi.org/10.1016/j.redox.2023.102624 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Articles from the Special Issue on Recent advances in sulfur biology and chemistry, Edited by: Dr. Peter Nagy
Alam, Md Morshedul
Kishino, Akihiro
Sung, Eunkyu
Sekine, Hiroki
Abe, Takaaki
Murakami, Shohei
Akaike, Takaaki
Motohashi, Hozumi
Contribution of NRF2 to sulfur metabolism and mitochondrial activity
title Contribution of NRF2 to sulfur metabolism and mitochondrial activity
title_full Contribution of NRF2 to sulfur metabolism and mitochondrial activity
title_fullStr Contribution of NRF2 to sulfur metabolism and mitochondrial activity
title_full_unstemmed Contribution of NRF2 to sulfur metabolism and mitochondrial activity
title_short Contribution of NRF2 to sulfur metabolism and mitochondrial activity
title_sort contribution of nrf2 to sulfur metabolism and mitochondrial activity
topic Articles from the Special Issue on Recent advances in sulfur biology and chemistry, Edited by: Dr. Peter Nagy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9941419/
https://www.ncbi.nlm.nih.gov/pubmed/36758466
http://dx.doi.org/10.1016/j.redox.2023.102624
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