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GCN5L1-mediated acetylation prevents Rictor degradation in cardiac cells after hypoxic stress
Cardiomyocyte apoptosis and cardiac fibrosis are the leading causes of mortality in patients with ischemic heart disease. As such, these processes represent potential therapeutic targets to treat heart failure resulting from ischemic insult. We previously demonstrated that the mitochondrial acetyltr...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10634848/ https://www.ncbi.nlm.nih.gov/pubmed/37961692 http://dx.doi.org/10.1101/2023.10.26.564170 |
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author | Bugga, Paramesha Manning, Janet R. Mushala, Bellina A.S. Stoner, Michael W. Sembrat, John Scott, Iain |
author_facet | Bugga, Paramesha Manning, Janet R. Mushala, Bellina A.S. Stoner, Michael W. Sembrat, John Scott, Iain |
author_sort | Bugga, Paramesha |
collection | PubMed |
description | Cardiomyocyte apoptosis and cardiac fibrosis are the leading causes of mortality in patients with ischemic heart disease. As such, these processes represent potential therapeutic targets to treat heart failure resulting from ischemic insult. We previously demonstrated that the mitochondrial acetyltransferase protein GCN5L1 regulates cardiomyocyte cytoprotective signaling in ischemia-reperfusion injury in vivo and hypoxia-reoxygenation injury in vitro. The current study investigated the mechanism underlying GCN5L1-mediated regulation of the Akt/mTORC2 cardioprotective signaling pathway. Rictor protein levels in cardiac tissues from human ischemic heart disease patients were significantly decreased relative to non-ischemic controls. Rictor protein levels were similarly decreased in cardiac AC16 cells following hypoxic stress, while mRNA levels remained unchanged. The reduction in Rictor protein levels after hypoxia was enhanced by the knockdown of GCN5L1, and was blocked by GCN5L1 overexpression. These findings correlated with changes in Rictor lysine acetylation, which were mediated by GCN5L1 acetyltransferase activity. Rictor degradation was regulated by proteasomal activity, which was antagonized by increased Rictor acetylation. Finally, we found that GCN5L1 knockdown restricted cytoprotective Akt signaling, in conjunction with decreased mTOR abundance and activity. In summary, these studies suggest that GCN5L1 promotes cardioprotective Akt/mTORC2 signaling by maintaining Rictor protein levels through enhanced lysine acetylation. |
format | Online Article Text |
id | pubmed-10634848 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-106348482023-11-13 GCN5L1-mediated acetylation prevents Rictor degradation in cardiac cells after hypoxic stress Bugga, Paramesha Manning, Janet R. Mushala, Bellina A.S. Stoner, Michael W. Sembrat, John Scott, Iain bioRxiv Article Cardiomyocyte apoptosis and cardiac fibrosis are the leading causes of mortality in patients with ischemic heart disease. As such, these processes represent potential therapeutic targets to treat heart failure resulting from ischemic insult. We previously demonstrated that the mitochondrial acetyltransferase protein GCN5L1 regulates cardiomyocyte cytoprotective signaling in ischemia-reperfusion injury in vivo and hypoxia-reoxygenation injury in vitro. The current study investigated the mechanism underlying GCN5L1-mediated regulation of the Akt/mTORC2 cardioprotective signaling pathway. Rictor protein levels in cardiac tissues from human ischemic heart disease patients were significantly decreased relative to non-ischemic controls. Rictor protein levels were similarly decreased in cardiac AC16 cells following hypoxic stress, while mRNA levels remained unchanged. The reduction in Rictor protein levels after hypoxia was enhanced by the knockdown of GCN5L1, and was blocked by GCN5L1 overexpression. These findings correlated with changes in Rictor lysine acetylation, which were mediated by GCN5L1 acetyltransferase activity. Rictor degradation was regulated by proteasomal activity, which was antagonized by increased Rictor acetylation. Finally, we found that GCN5L1 knockdown restricted cytoprotective Akt signaling, in conjunction with decreased mTOR abundance and activity. In summary, these studies suggest that GCN5L1 promotes cardioprotective Akt/mTORC2 signaling by maintaining Rictor protein levels through enhanced lysine acetylation. Cold Spring Harbor Laboratory 2023-10-26 /pmc/articles/PMC10634848/ /pubmed/37961692 http://dx.doi.org/10.1101/2023.10.26.564170 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Bugga, Paramesha Manning, Janet R. Mushala, Bellina A.S. Stoner, Michael W. Sembrat, John Scott, Iain GCN5L1-mediated acetylation prevents Rictor degradation in cardiac cells after hypoxic stress |
title | GCN5L1-mediated acetylation prevents Rictor degradation in cardiac cells after hypoxic stress |
title_full | GCN5L1-mediated acetylation prevents Rictor degradation in cardiac cells after hypoxic stress |
title_fullStr | GCN5L1-mediated acetylation prevents Rictor degradation in cardiac cells after hypoxic stress |
title_full_unstemmed | GCN5L1-mediated acetylation prevents Rictor degradation in cardiac cells after hypoxic stress |
title_short | GCN5L1-mediated acetylation prevents Rictor degradation in cardiac cells after hypoxic stress |
title_sort | gcn5l1-mediated acetylation prevents rictor degradation in cardiac cells after hypoxic stress |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10634848/ https://www.ncbi.nlm.nih.gov/pubmed/37961692 http://dx.doi.org/10.1101/2023.10.26.564170 |
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