Physiologic Responses to Dietary Sulfur Amino Acid Restriction in Mice Are Influenced by Atf4 Status and Biological Sex

Author:

Jonsson William O1ORCID,Margolies Nicholas S1ORCID,Mirek Emily T1ORCID,Zhang Qian2,Linden Melissa A23ORCID,Hill Cristal M3ORCID,Link Christopher4,Bithi Nazmin4ORCID,Zalma Brian1ORCID,Levy Jordan L1ORCID,Pettit Ashley P1ORCID,Miller Joshua W1ORCID,Hine Christopher4ORCID,Morrison Christopher D3ORCID,Gettys Thomas W3ORCID,Miller Benjamin F5ORCID,Hamilton Karyn L2ORCID,Wek Ronald C6ORCID,Anthony Tracy G1ORCID

Affiliation:

1. Department of Nutritional Sciences, Rutgers University, New Brunswick, NJ, USA

2. Department of Health and Exercise Science, Colorado State University, Ft. Collins, CO, USA

3. Pennington Biomedical Research Center, Louisiana State University, Baton Rouge, LA, USA

4. Department of Cardiovascular and Metabolic Sciences, Cleveland Clinic Lerner Research Institute, Cleveland, OH, USA

5. Aging & Metabolism Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA

6. Department of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, IN, USA

Abstract

ABSTRACT 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.

Funder

NIH

USDA

National Institute of Food and Agriculture

Publisher

Oxford University Press (OUP)

Subject

Nutrition and Dietetics,Medicine (miscellaneous)

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