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Status: Bibliographieeintrag

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Verfasst von:Drekolia, Maria-Kyriaki [VerfasserIn]   i
 Karantanou, Christina [VerfasserIn]   i
 Wittig, Ilka [VerfasserIn]   i
 Li, Yuanyuan [VerfasserIn]   i
 Fuhrmann, Dominik C. [VerfasserIn]   i
 Brüne, Bernhard [VerfasserIn]   i
 Katsouda, Antonia [VerfasserIn]   i
 Hu, Jiong [VerfasserIn]   i
 Papapetropoulos, Andreas [VerfasserIn]   i
 Bibli, Sofia-Iris [VerfasserIn]   i
Titel:Loss of cardiac mitochondrial complex I persulfidation impairs NAD+ homeostasis in aging
Verf.angabe:Maria-Kyriaki Drekolia, Christina Karantanou, Ilka Wittig, Yuanyuan Li, Dominik C. Fuhrmann, Bernhard Brüne, Antonia Katsouda, Jiong Hu, Andreas Papapetropoulos, Sofia-Iris Bibli
Jahr:2024
Umfang:8 S.
Illustrationen:Illustrationen
Fussnoten:Online verfügbar: 25 December 2023 ; Im Titel ist "+" hochgestellt ; Gesehen am 10.09.2024
Titel Quelle:Enthalten in: Redox Biology
Ort Quelle:Amsterdam [u.a.] : Elsevier, 2013
Jahr Quelle:2024
Band/Heft Quelle:69(2024) vom: Jan., Artikel-ID 1030144, Seite 1-8
ISSN Quelle:2213-2317
Abstract:Protein persulfidation is a significant post-translational modification that involves addition of a sulfur atom to the cysteine thiol group and is facilitated by sulfide species. Persulfidation targets reactive cysteine residues within proteins, influencing their structure and/or function across various biological systems. This modification is evolutionarily conserved and plays a crucial role in preventing irreversible cysteine overoxidation, a process that becomes prominent with aging. While, persulfidation decreases with age, its levels in the aged heart and the functional implications of such a reduction in cardiac metabolism remain unknown. Here we interrogated the cardiac persulfydome in wild-type adult mice and age-matched mice lacking the two sulfide generating enzymes, namely cystathionine gamma lyase (CSE) and 3-mercaptopyruvate sulfurtransferase (3MST). Our findings revealed that cardiac persulfidated proteins in wild type hearts are less abundant compared to those in other organs, with a primary involvement in mitochondrial metabolic processes. We further focused on one specific target, NDUFB7, which undergoes persulfidation by both CSE and 3MST derived sulfide species. In particular, persulfidation of cysteines C80 and C90 in NDUFB7 protects the protein from overoxidation and maintains the complex I activity in cardiomyocytes. As the heart ages, the levels of CSE and 3MST in cardiomyocytes decline, leading to reduced NDUFB7 persulfidation and increased cardiac NADH/NAD+ ratio. Collectively, our data provide compelling evidence for a direct link between cardiac persulfidation and mitochondrial complex I activity, which is compromised in aging.
DOI:doi:10.1016/j.redox.2023.103014
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext: https://doi.org/10.1016/j.redox.2023.103014
 DOI: https://doi.org/10.1016/j.redox.2023.103014
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:3MST
 Aging
 Animals
 Cardiac aging
 CSE
 Cysteine
 Homeostasis
 Hydrogen Sulfide
 Mice
 NAD
 NDUFB7
 Persulfidation
 Sulfides
K10plus-PPN:1902256190
Verknüpfungen:→ Zeitschrift

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