<scp>SIRT3</scp> deficiency decreases oxidative metabolism capacity but increases lifespan in male mice under caloric restriction-Reference-Cited by-同舟云学术

SIRT3 deficiency decreases oxidative metabolism capacity but increases lifespan in male mice under caloric restriction

Published:2022-10-05 Issue:12 Volume:21 Page:
ISSN:1474-9718
Container-title:Aging Cell
language:en
Short-container-title:Aging Cell

Author:

Dhillon Rashpal S.¹²,Qin Yiming (Amy)¹²³^ORCID,van Ginkel Paul R.⁴,Fu Vivian X.⁴,Vann James M.⁴,Lawton Alexis J.¹²,Green Cara L.⁵⁶,Manchado‐Gobatto Fúlvia B.⁷,Gobatto Claudio A.⁷,Lamming Dudley W.³⁵⁶,Prolla Tomas A.⁴,Denu John M.¹²³

Affiliation:

1. Department of Biomolecular Chemistry University of Wisconsin‐Madison Madison Wisconsin USA

2. Wisconsin Institute for Discovery University of Wisconsin‐Madison Madison Wisconsin USA

3. Interdepartmental Graduate Program in Nutritional Sciences University of Wisconsin‐Madison Madison Wisconsin USA

4. Department of Genetics and Medical Genetics University of Wisconsin‐Madison Madison Wisconsin USA

5. Department of Medicine, SMPH University of Wisconsin‐Madison Madison Wisconsin USA

6. William S. Middleton Memorial Veterans Hospital Madison Wisconsin USA

7. Laboratory of Applied Sport Physiology, School of Applied Sciences University of Campinas Limeira Brazil

Funder

American Federation for Aging Research

National Institute of Diabetes and Digestive and Kidney Diseases

National Institute on Aging

U.S. Department of Veterans Affairs

Fundação de Amparo à Pesquisa do Estado de São Paulo

Publisher

Wiley

Subject

Cell Biology,Aging

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/acel.13721

Reference74 articles.

1. Mice under Caloric Restriction Self-Impose a Temporal Restriction of Food Intake as Revealed by an Automated Feeder System

2. A role for the mitochondrial deacetylase Sirt3 in regulating energy homeostasis

3. Function of the SIRT3 mitochondrial deacetylase in cellular physiology, cancer, and neurodegenerative disease

4. Revealing Dynamic Protein Acetylation across Subcellular Compartments

5. Mechanisms and Dynamics of Protein Acetylation in Mitochondria

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