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Late life-applicable enhancement of longevity and fitness.

Descrizione del progetto

Comprendere l’invecchiamento, esplorare soluzioni terapeutiche

La causa principale dell’invecchiamento è il graduale declino delle funzioni cellulari e molecolari. Con l’avanzare dell’età, la nostra capacità di adattarci ai fattori di stress e di riparare il nostro corpo diminuisce, il che limita l’efficacia dei trattamenti anti-invecchiamento come la metformina, le restrizioni alimentari e l’esercizio fisico. L’obiettivo del progetto LifeLongFit, finanziato dal CER, è quello di impiegare la multiomica e i test funzionali in vari organismi per approfondire i problemi legati all’invecchiamento e studiare potenziali soluzioni terapeutiche. Il progetto mira a scoprire i meccanismi intrinseci di resilienza contro la tossicità tardiva della metformina e i fattori di stress adattativi nei nematodi. Lo studio indagherà inoltre sui fattori che contribuiscono all’eccezionale longevità di mammiferi come l’eterocefalo glabro e le balene attraverso l’analisi dei dati omici.

Obiettivo

Aging represents gradual organismal decline driven by accumulation of cellular and molecular damages including DNA damage and metabolic failures. At young and middle age, these damages are mitigated by tailored repair systems, such as autophagy and DNA damage response. The repairs can be triggered through adaptive stress responses induced by anti-aging interventions such as dietary restriction (DR) and DR mimetic metformin. Recently, we found that loss of metabolic plasticity and repair activities due to aging abrogate longevity benefits of adaptive stressors at old age. Specifically, we found that aging-linked failures of mitochondria and lipid catabolism limit metformin benefits and confer metformin toxicity in late life, and others showed comparable limitations for DR and exercise. Our findings demonstrate that anti-aging treatments do lose efficacy in old organisms, and new approaches are required to promote healthy aging in late life.
Here, we will use multi-omics, and functional tests in C. elegans, short-lived killifish and long-lived mammals to (a) probe the origin of aging-linked adaptive failures and (b) find molecular and therapeutic solutions for overcoming these failures. Omics tests and survival screens will be used to uncover mechanisms of intrinsic resilience against late life toxicity of metformin and other adaptive stressors in nematodes. Additional omics data will be analyzed to probe adaptive basis of the exceptional mammalian longevity in NMR and whale, followed by attempted replication of uncovered differences in shorter-lived species (nematodes and fish) by drugs and gene changes, with an outlook of triggering superior stress resilience and metabolic plasticity in late life. Our expertise will allow testing late life responses to diverse adaptive interventions from moderate genotoxic stress to DR mimetics and microbiome manipulation. This innovative program will illuminate novel treatments for healthy longevity that are not limited by aging.

Meccanismo di finanziamento

HORIZON-ERC - HORIZON ERC Grants

Istituzione ospitante

LEIBNIZ-INSTITUT FUR ALTERNSFORSCHUNG - FRITZ-LIPMANN-INSTITUT EV (FLI) LEIBNIZ INSTITUTE ON AGING - FRITZ LIPMANN INSTITUTE EV (FLI)
Contribution nette de l'UE
€ 2 000 000,00
Indirizzo
BEUTENBERGSTRASSE 11
07745 Jena
Germania

Mostra sulla mappa

Regione
Thüringen Thüringen Jena, Kreisfreie Stadt
Tipo di attività
Research Organisations
Collegamenti
Costo totale
€ 2 000 000,00

Beneficiari (1)