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author Asantewaa, Gloria
Tuttle, Emily T.
Ward, Nathan P.
Kang, Yun Pyo
Kim, Yumi
Kavanagh, Madeline E.
Girnius, Nomeda
Chen, Ying
Duncan, Renae
Rodriguez, Katherine
Hecht, Fabio
Zocchi, Marco
Smorodintsev-Schiller, Leonid
Scales, TashJaé Q.
Taylor, Kira
Alimohammadi, Fatemeh
Sechrist, Zachary R
Agostini-Vulaj, Diana
Schafer, Xenia L.
Chang, Hayley
Smith, Zachary
O’Connor, Thomas N.
Whelan, Sarah
Selfors, Laura M.
Crowdis, Jett
Gray, G. Kenneth
Bronson, Roderick T.
Brenner, Dirk
Rufini, Alessandro
Dirksen, Robert T.
Hezel, Aram F.
Huber, Aaron R.
Munger, Josh
Cravatt, Benjamin F.
Vasiliou, Vasilis
Cole, Calvin L
DeNicola, Gina M.
Harris, Isaac S.
author_facet Asantewaa, Gloria
Tuttle, Emily T.
Ward, Nathan P.
Kang, Yun Pyo
Kim, Yumi
Kavanagh, Madeline E.
Girnius, Nomeda
Chen, Ying
Duncan, Renae
Rodriguez, Katherine
Hecht, Fabio
Zocchi, Marco
Smorodintsev-Schiller, Leonid
Scales, TashJaé Q.
Taylor, Kira
Alimohammadi, Fatemeh
Sechrist, Zachary R
Agostini-Vulaj, Diana
Schafer, Xenia L.
Chang, Hayley
Smith, Zachary
O’Connor, Thomas N.
Whelan, Sarah
Selfors, Laura M.
Crowdis, Jett
Gray, G. Kenneth
Bronson, Roderick T.
Brenner, Dirk
Rufini, Alessandro
Dirksen, Robert T.
Hezel, Aram F.
Huber, Aaron R.
Munger, Josh
Cravatt, Benjamin F.
Vasiliou, Vasilis
Cole, Calvin L
DeNicola, Gina M.
Harris, Isaac S.
author_sort Asantewaa, Gloria
collection PubMed
description Cells rely on antioxidants to survive. The most abundant antioxidant is glutathione (GSH). The synthesis of GSH is non-redundantly controlled by the glutamate-cysteine ligase catalytic subunit (GCLC). GSH imbalance is implicated in many diseases, but the requirement for GSH in adult tissues is unclear. To interrogate this, we developed a series of in vivo models to induce Gclc deletion in adult animals. We find that GSH is essential to lipid abundance in vivo. GSH levels are reported to be highest in liver tissue, which is also a hub for lipid production. While the loss of GSH did not cause liver failure, it decreased lipogenic enzyme expression, circulating triglyceride levels, and fat stores. Mechanistically, we found that GSH promotes lipid abundance by repressing NRF2, a transcription factor induced by oxidative stress. These studies identify GSH as a fulcrum in the liver’s balance of redox buffering and triglyceride production.
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spelling pubmed-99345952023-02-17 Glutathione supports lipid abundance in vivo Asantewaa, Gloria Tuttle, Emily T. Ward, Nathan P. Kang, Yun Pyo Kim, Yumi Kavanagh, Madeline E. Girnius, Nomeda Chen, Ying Duncan, Renae Rodriguez, Katherine Hecht, Fabio Zocchi, Marco Smorodintsev-Schiller, Leonid Scales, TashJaé Q. Taylor, Kira Alimohammadi, Fatemeh Sechrist, Zachary R Agostini-Vulaj, Diana Schafer, Xenia L. Chang, Hayley Smith, Zachary O’Connor, Thomas N. Whelan, Sarah Selfors, Laura M. Crowdis, Jett Gray, G. Kenneth Bronson, Roderick T. Brenner, Dirk Rufini, Alessandro Dirksen, Robert T. Hezel, Aram F. Huber, Aaron R. Munger, Josh Cravatt, Benjamin F. Vasiliou, Vasilis Cole, Calvin L DeNicola, Gina M. Harris, Isaac S. bioRxiv Article Cells rely on antioxidants to survive. The most abundant antioxidant is glutathione (GSH). The synthesis of GSH is non-redundantly controlled by the glutamate-cysteine ligase catalytic subunit (GCLC). GSH imbalance is implicated in many diseases, but the requirement for GSH in adult tissues is unclear. To interrogate this, we developed a series of in vivo models to induce Gclc deletion in adult animals. We find that GSH is essential to lipid abundance in vivo. GSH levels are reported to be highest in liver tissue, which is also a hub for lipid production. While the loss of GSH did not cause liver failure, it decreased lipogenic enzyme expression, circulating triglyceride levels, and fat stores. Mechanistically, we found that GSH promotes lipid abundance by repressing NRF2, a transcription factor induced by oxidative stress. These studies identify GSH as a fulcrum in the liver’s balance of redox buffering and triglyceride production. Cold Spring Harbor Laboratory 2023-02-11 /pmc/articles/PMC9934595/ /pubmed/36798186 http://dx.doi.org/10.1101/2023.02.10.524960 Text en https://creativecommons.org/licenses/by-nd/4.0/This work is licensed under a Creative Commons Attribution-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, and only so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Article
Asantewaa, Gloria
Tuttle, Emily T.
Ward, Nathan P.
Kang, Yun Pyo
Kim, Yumi
Kavanagh, Madeline E.
Girnius, Nomeda
Chen, Ying
Duncan, Renae
Rodriguez, Katherine
Hecht, Fabio
Zocchi, Marco
Smorodintsev-Schiller, Leonid
Scales, TashJaé Q.
Taylor, Kira
Alimohammadi, Fatemeh
Sechrist, Zachary R
Agostini-Vulaj, Diana
Schafer, Xenia L.
Chang, Hayley
Smith, Zachary
O’Connor, Thomas N.
Whelan, Sarah
Selfors, Laura M.
Crowdis, Jett
Gray, G. Kenneth
Bronson, Roderick T.
Brenner, Dirk
Rufini, Alessandro
Dirksen, Robert T.
Hezel, Aram F.
Huber, Aaron R.
Munger, Josh
Cravatt, Benjamin F.
Vasiliou, Vasilis
Cole, Calvin L
DeNicola, Gina M.
Harris, Isaac S.
Glutathione supports lipid abundance in vivo
title Glutathione supports lipid abundance in vivo
title_full Glutathione supports lipid abundance in vivo
title_fullStr Glutathione supports lipid abundance in vivo
title_full_unstemmed Glutathione supports lipid abundance in vivo
title_short Glutathione supports lipid abundance in vivo
title_sort glutathione supports lipid abundance in vivo
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9934595/
https://www.ncbi.nlm.nih.gov/pubmed/36798186
http://dx.doi.org/10.1101/2023.02.10.524960
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