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Physiologic Responses to Dietary Sulfur Amino Acid Restriction in Mice Are Influenced by Atf4 Status and Biological Sex
BACKGROUND: Dietary sulfur amino acid restriction (SAAR) improves body composition and metabolic health across several model organisms in part through induction of the integrated stress response (ISR). OBJECTIVE: We investigate the hypothesis that activating transcription factor 4 (ATF4) acts as a c...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8030708/ https://www.ncbi.nlm.nih.gov/pubmed/33512502 http://dx.doi.org/10.1093/jn/nxaa396 |
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author | Jonsson, William O Margolies, Nicholas S Mirek, Emily T Zhang, Qian Linden, Melissa A Hill, Cristal M Link, Christopher Bithi, Nazmin Zalma, Brian Levy, Jordan L Pettit, Ashley P Miller, Joshua W Hine, Christopher Morrison, Christopher D Gettys, Thomas W Miller, Benjamin F Hamilton, Karyn L Wek, Ronald C Anthony, Tracy G |
author_facet | Jonsson, William O Margolies, Nicholas S Mirek, Emily T Zhang, Qian Linden, Melissa A Hill, Cristal M Link, Christopher Bithi, Nazmin Zalma, Brian Levy, Jordan L Pettit, Ashley P Miller, Joshua W Hine, Christopher Morrison, Christopher D Gettys, Thomas W Miller, Benjamin F Hamilton, Karyn L Wek, Ronald C Anthony, Tracy G |
author_sort | Jonsson, William O |
collection | PubMed |
description | BACKGROUND: Dietary sulfur amino acid restriction (SAAR) improves body composition and metabolic health across several model organisms in part through induction of the integrated stress response (ISR). OBJECTIVE: We investigate the hypothesis that activating transcription factor 4 (ATF4) acts as a converging point in the ISR during SAAR. METHODS: Using liver-specific or global gene ablation strategies, in both female and male mice, we address the role of ATF4 during dietary SAAR. RESULTS: We show that ATF4 is dispensable in the chronic induction of the hepatokine fibroblast growth factor 21 while being essential for the sustained production of endogenous hydrogen sulfide. We also affirm that biological sex, independent of ATF4 status, is a determinant of the response to dietary SAAR. CONCLUSIONS: Our results suggest that auxiliary components of the ISR, which are independent of ATF4, are critical for SAAR-mediated improvements in metabolic health in mice. |
format | Online Article Text |
id | pubmed-8030708 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-80307082021-04-14 Physiologic Responses to Dietary Sulfur Amino Acid Restriction in Mice Are Influenced by Atf4 Status and Biological Sex Jonsson, William O Margolies, Nicholas S Mirek, Emily T Zhang, Qian Linden, Melissa A Hill, Cristal M Link, Christopher Bithi, Nazmin Zalma, Brian Levy, Jordan L Pettit, Ashley P Miller, Joshua W Hine, Christopher Morrison, Christopher D Gettys, Thomas W Miller, Benjamin F Hamilton, Karyn L Wek, Ronald C Anthony, Tracy G J Nutr Biochemical, Molecular, and Genetic Mechanisms BACKGROUND: Dietary sulfur amino acid restriction (SAAR) improves body composition and metabolic health across several model organisms in part through induction of the integrated stress response (ISR). OBJECTIVE: We investigate the hypothesis that activating transcription factor 4 (ATF4) acts as a converging point in the ISR during SAAR. METHODS: Using liver-specific or global gene ablation strategies, in both female and male mice, we address the role of ATF4 during dietary SAAR. RESULTS: We show that ATF4 is dispensable in the chronic induction of the hepatokine fibroblast growth factor 21 while being essential for the sustained production of endogenous hydrogen sulfide. We also affirm that biological sex, independent of ATF4 status, is a determinant of the response to dietary SAAR. CONCLUSIONS: Our results suggest that auxiliary components of the ISR, which are independent of ATF4, are critical for SAAR-mediated improvements in metabolic health in mice. Oxford University Press 2021-01-29 /pmc/articles/PMC8030708/ /pubmed/33512502 http://dx.doi.org/10.1093/jn/nxaa396 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the American Society for Nutrition. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Biochemical, Molecular, and Genetic Mechanisms Jonsson, William O Margolies, Nicholas S Mirek, Emily T Zhang, Qian Linden, Melissa A Hill, Cristal M Link, Christopher Bithi, Nazmin Zalma, Brian Levy, Jordan L Pettit, Ashley P Miller, Joshua W Hine, Christopher Morrison, Christopher D Gettys, Thomas W Miller, Benjamin F Hamilton, Karyn L Wek, Ronald C Anthony, Tracy G Physiologic Responses to Dietary Sulfur Amino Acid Restriction in Mice Are Influenced by Atf4 Status and Biological Sex |
title | Physiologic Responses to Dietary Sulfur Amino Acid Restriction in Mice Are Influenced by Atf4 Status and Biological Sex |
title_full | Physiologic Responses to Dietary Sulfur Amino Acid Restriction in Mice Are Influenced by Atf4 Status and Biological Sex |
title_fullStr | Physiologic Responses to Dietary Sulfur Amino Acid Restriction in Mice Are Influenced by Atf4 Status and Biological Sex |
title_full_unstemmed | Physiologic Responses to Dietary Sulfur Amino Acid Restriction in Mice Are Influenced by Atf4 Status and Biological Sex |
title_short | Physiologic Responses to Dietary Sulfur Amino Acid Restriction in Mice Are Influenced by Atf4 Status and Biological Sex |
title_sort | physiologic responses to dietary sulfur amino acid restriction in mice are influenced by atf4 status and biological sex |
topic | Biochemical, Molecular, and Genetic Mechanisms |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8030708/ https://www.ncbi.nlm.nih.gov/pubmed/33512502 http://dx.doi.org/10.1093/jn/nxaa396 |
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