Open AccessModulating the integrated stress response to slow aging and ameliorate age-related pathology
Author(s) -
Maxime Derisbourg,
Matías D. Hartman,
Martin S. Denzel
Publication year - 2021
Publication title -
nature aging
Language(s) - English
Resource type - Journals
ISSN - 2662-8465
DOI - 10.1038/s43587-021-00112-9
Subject(s) - translation (biology) , longevity , integrated stress response , biology , phosphorylation , ageing , protein subunit , senescence , microbiology and biotechnology , protein biosynthesis , eif2 , neuroscience , psychology , gerontology , messenger rna , medicine , genetics , gene
Healthy aging requires the coordination of numerous stress signaling pathways that converge on the protein homeostasis network. The Integrated Stress Response (ISR) is activated by diverse stimuli, leading to phosphorylation of the eukaryotic translation initiation factor elF2 in its α-subunit. Under replete conditions, elF2 orchestrates 5' cap-dependent mRNA translation and is thus responsible for general protein synthesis. elF2α phosphorylation, the key event of the ISR, reduces global mRNA translation while enhancing the expression of a signature set of stress response genes. Despite the critical role of protein quality control in healthy aging and in numerous longevity pathways, the role of the ISR in longevity remains largely unexplored. ISR activity increases with age, suggesting a potential link with the aging process. Although decreased protein biosynthesis, which occurs during ISR activation, have been linked to lifespan extension, recent data show that lifespan is limited by the ISR as its inhibition extends survival in nematodes and enhances cognitive function in aged mice. Here we survey how aging affects the ISR, the role of the ISR in modulating aging, and pharmacological interventions to tune the ISR. Finally, we will explore the ISR as a plausible target for clinical interventions in aging and age-related disease.