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EnCAge TERMINATED

Progeria models to study endothelial cell ageing: implications for organ regeneration and fibrosis

Total Cost €

0

EC-Contrib. €

0

Partnership

0

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 EnCAge project word cloud

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

screenings    expression    syndrome    phenotype    provoking    hgps    ageing    disorders    mouse    candidate    lost    progerin    age    repair    levels    remarkably    protein    expensive    fibrosis    model    premature    organ    nuclear    time    ec    liver    play    therapeutic    fibrotic    specialized    impairment    health    mechanisms    acquisition    induces    guide    aged    regeneration    cells    vitro    recapitulate    ecs    compounds    proven    throughput    models    injury    experimental    mutant    tissue    consuming    mimics    prominent    passive    regulate    disease    compromise    dependent    elicit    hutchinson    angiocrine    cell    homeostasis    dysfunction    blood    drugs    self    modelled    functions    reverse    detected    practical    gilford    prelamin    societies    renewal    delivering    physiological    human    mice    tackle    individuals    tissues    alterations    form    capillary    instructive    endothelial    convenient    progeria    conduits    rare    prevent    causal    stem    caused   

Project "EnCAge" data sheet

The following table provides information about the project.

Coordinator
CENTRO NACIONAL DE INVESTIGACIONESCARDIOVASCULARES CARLOS III (F.S.P.) 

Organization address
address: CALLE MELCHOR FERNANDEZ ALMAGRO 3
city: MADRID
postcode: 28029
website: www.cnic.es

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 Spain [ES]
 Total cost 170˙121 €
 EC max contribution 170˙121 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2017
 Funding Scheme MSCA-IF-EF-RI
 Starting year 2020
 Duration (year-month-day) from 2020-02-01   to  2022-01-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    CENTRO NACIONAL DE INVESTIGACIONESCARDIOVASCULARES CARLOS III (F.S.P.) ES (MADRID) coordinator 170˙121.00

Map

 Project objective

Capillary endothelial cells (ECs) are not just passive conduits for delivering blood. Rather, ECs also play tissue-specific functions by providing highly specialized sets of angiocrine factors that control tissue homeostasis, regulate stem cell self-renewal, and guide organ regeneration without provoking fibrosis. However, it is not known whether tissue-specific instructive functions of ECs are lost during ageing. Moreover, the causal role of EC ageing in age-associated tissue dysfunction has not been directly studied so far. The use of aged mice to study age-related tissue alterations and to develop new drugs is not practical, since it is expensive, time consuming and does not allow for high throughput screenings. Thus, it is key to develop more convenient experimental systems that recapitulate the phenotype of aged cells. Hutchinson-Gilford progeria syndrome (HGPS) is a rare disease caused by progerin, a mutant form of the nuclear protein prelamin A that induces premature ageing. Remarkably, HGPS mimics many of the characteristics of human ageing, and progerin has also been detected at low levels in aged tissues of non-HGPS individuals. Thus, HGPS experimental models have proven to be very useful for the study of physiological ageing. This proposal will study age-dependent and tissue-specific alterations in ECs using a mouse model of HGPS. Furthermore, the candidate will use mice with EC-specific expression of progerin to assess the causal role of EC ageing in age-related impairment of organ regeneration, modelled by liver repair after injury. Finally, the applicant will develop an in vitro system to identify mechanisms through which progerin-induced EC ageing may elicit fibrotic responses that could compromise organ repair, and to test compounds to prevent or reverse the acquisition of an aged EC phenotype. These studies will open new potential therapeutic approaches to tackle age-related disorders, one of the most prominent health issues in European societies.

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The information about "ENCAGE" are provided by the European Opendata Portal: CORDIS opendata.

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