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ComBATageing SIGNED

Exploiting superlongevous model mammals to explore new links between protein and organelle homeostasis and lifespan extension

Total Cost €

0

EC-Contrib. €

0

Partnership

0

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 ComBATageing project word cloud

Explore the words cloud of the ComBATageing project. It provides you a very rough idea of what is the project "ComBATageing" about.

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Project "ComBATageing" data sheet

The following table provides information about the project.

Coordinator
OSPEDALE SAN RAFFAELE SRL 

Organization address
address: VIA OLGETTINA 60
city: MILANO
postcode: 20132
website: www.hsr.it

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country Italy [IT]
 Total cost 183˙473 €
 EC max contribution 183˙473 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2019
 Funding Scheme MSCA-IF-EF-SE
 Starting year 2021
 Duration (year-month-day) from 2021-09-01   to  2023-08-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    OSPEDALE SAN RAFFAELE SRL IT (MILANO) coordinator 183˙473.00

Map

 Project objective

Despite being one of the most familiar biological process affecting our lives, little is known about the molecular mechanics of ageing. A better understanding of ageing and related diseases is today crucial to face its deleterious effects on our growing older population. Among mammals bigger species typically live longer than smaller ones. When corrected for body size, almost all mammals have the same longevity quotients, exception made for the chiroptera. Bats are capable of living up to 10 times longer than expected despite their characteristic high metabolic rates. During my doctorate, I discovered the presence of a distinctive behaviour in bats' autophagic pathway, suggesting that these animals may rely on an improved system for intracellular proteostasis accounting for the flight-associated high metabolic stress. The same evolutive adaptation could ultimately have played a role in allowing bats to achieve exceptional longevity. Here I propose to carry out an in-depth analysis of the proteostatic system, and in particular of the autophagic pathway, in bats. Samples from wild populations of bats will be used to derive primary cell lines allowing to characterise bats’ intracellular phenotype and proteostatic activity. Thanks to the expert personnel and cutting-edge facilities of the hosting institute, I will exploit imaging and proteomics tools to isolate bat-specific molecular features of adaptation in proteostasis and unveil their role in determining their unique ageing pattern. A complementary phylogenomic analysis will be performed to detect traces of adaptive selection in proteostasis-associated genes in bats and other mammals. For the first time, the complexity of interactions behind proteostasis and ageing will be examined from a privileged, integrative perspective. This innovative project holds huge potential as it could lead to a greater understanding of the role of protein homeostasis in mammalian ageing contributing to dampen its effects on our society.

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