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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
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.
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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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