AMPK-mediated formation of stress granules is required for dietary restriction-induced longevity in Caenorhabditis elegans.


Journal

Aging cell
ISSN: 1474-9726
Titre abrégé: Aging Cell
Pays: England
ID NLM: 101130839

Informations de publication

Date de publication:
06 2020
Historique:
received: 25 09 2019
revised: 07 03 2020
accepted: 08 04 2020
pubmed: 21 5 2020
medline: 14 7 2021
entrez: 21 5 2020
Statut: ppublish

Résumé

Stress granules (SGs) are nonmembranous organelles that are dynamically assembled and disassembled in response to various stressors. Under stressed conditions, polyadenylated mRNAs and translation factors are sequestrated in SGs to promote global repression of protein synthesis. It has been previously demonstrated that SG formation enhances cell survival and stress resistance. However, the physiological role of SGs in organismal aging and longevity regulation remains unclear. In this study, we used TIAR-1::GFP and GTBP-1::GFP as markers to monitor the formation of SGs in Caenorhabditis elegans. We found that, in addition to acute heat stress, SG formation could also be triggered by dietary changes, such as starvation and dietary restriction (DR). We found that HSF-1 is required for the SG formation in response to acute heat shock and starvation but not DR, whereas the AMPK-eEF2K signaling is required for starvation and DR-induced SG formation but not heat shock. Moreover, our data suggest that this AMPK-eEF2K pathway-mediated SG formation is required for lifespan extension by DR, but dispensable for the longevity by reduced insulin/IGF-1 signaling. Collectively, our findings unveil a novel role of SG formation in DR-induced longevity.

Identifiants

pubmed: 32432401
doi: 10.1111/acel.13157
pmc: PMC7294782
doi:

Substances chimiques

AMP-Activated Protein Kinases EC 2.7.11.31

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e13157

Informations de copyright

© 2020 The Authors. Aging Cell published by Anatomical Society and John Wiley & Sons Ltd.

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Auteurs

Chen-Ting Kuo (CT)

Institute of Biopharmaceutical Sciences, Yang-Ming University, Taipei, Taiwan.

Guan-Ting You (GT)

Institute of Biopharmaceutical Sciences, Yang-Ming University, Taipei, Taiwan.

Ying-Jie Jian (YJ)

Institute of Biopharmaceutical Sciences, Yang-Ming University, Taipei, Taiwan.

Ting-Shin Chen (TS)

Institute of Biopharmaceutical Sciences, Yang-Ming University, Taipei, Taiwan.

Yu-Chen Siao (YC)

Institute of Biochemistry and Molecular Biology, National Yang-Ming University, Taipei, Taiwan.

Ao-Lin Hsu (AL)

Institute of Biochemistry and Molecular Biology, National Yang-Ming University, Taipei, Taiwan.
Research Center for Healthy Aging and Institute of New Drug Development, China Medical University, Taichung, Taiwan.
Division of Geriatric and Palliative Medicine, Department of Internal Medicine, University of Michigan, Ann Arbor, MI, USA.

Tsui-Ting Ching (TT)

Institute of Biopharmaceutical Sciences, Yang-Ming University, Taipei, Taiwan.

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Classifications MeSH