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Superoxide signal orchestrates tetrathiomolybdate-induced longevity via ARGK-1 in Caenorhabditis elegans.

Authors :
Zhou Y
Zhang M
Lu S
Liu L
Duan Z
Wei F
Li G
Source :
Free radical biology & medicine [Free Radic Biol Med] 2024 Sep; Vol. 222, pp. 650-660. Date of Electronic Publication: 2024 Jul 16.
Publication Year :
2024

Abstract

Purpose: While reactive oxygen species (ROS) have been identified as key redox signaling agents contributing to aging process, which and how specific oxidants trigger healthy longevity remain unclear. This paper aimed to explore the precise role and signaling mechanism of superoxide (O <subscript>2</subscript> <superscript>•-</superscript> ) in health and longevity.<br />Methods: A tool for precise regulation of O <subscript>2</subscript> <superscript>•-</superscript> levels in vivo was developed based on the inhibition of superoxide dismutase 1 (SOD1) by tetrathiomolybdate (TM) in Caenorhabditis elegans (C. elegans). Then, we examined the effects of TM on lifespan, reproduction, lipofuscin accumulation, mobility, and stress resistance. Finally, the signaling mechanism for longevity induced by TM-O <subscript>2</subscript> <superscript>•-</superscript> was screened by transcriptome analysis and tested in sod-1 and argk-1 RNAi strains, sod-2, sod-3, and daf-16 mutants.<br />Results: TM promoted longevity in C. elegans with a concomitant extension of healthy lifespan as indicated by increasing fertility and mobility and reducing lipofuscin accumulation, as well as enhanced resistance to different abiotic stresses. Mechanically, TM could precisely regulate O <subscript>2</subscript> <superscript>•-</superscript> levels in nematodes via modulating SOD1 activity. An O <subscript>2</subscript> <superscript>•-</superscript> scavenger Mn(III)TBAP abolished TM-induced lifespan extension, while an O <subscript>2</subscript> <superscript>•-</superscript> generator paraquat at low concentration mimicked the life prolongation effects. The longevity in TM-treated worms was abolished by sod-1 RNAi but was not affected in sod-2 or sod-3 mutants. Further transcriptome analysis revealed arginine kinase ARGK-1 and its downstream insulin/insulin-like growth factor 1 signaling (IIS) as potential effectors for TM-O <subscript>2</subscript> <superscript>•‾</superscript> -induced longevity, and argk-1 RNAi or daf-16 mutant nullified the longevity.<br />Conclusions: These findings indicate that it is feasible to precisely control specific oxidant in vivo and O <subscript>2</subscript> <superscript>•-</superscript> orchestrates TM-induced health and longevity in C. elegans via ARGK-1-IIS axis.<br />Competing Interests: Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Guolin Li, Yiming Zhou, and Fang Wei have patent #2024106280781 pending to Hunan Normal University. If there are other authors, they declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2024 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1873-4596
Volume :
222
Database :
MEDLINE
Journal :
Free radical biology & medicine
Publication Type :
Academic Journal
Accession number :
39025156
Full Text :
https://doi.org/10.1016/j.freeradbiomed.2024.07.014