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PROGLUTASIS SIGNED

Protection of cardiometabolic inflammation by modulation of myeloid glutamine homeostasis

Total Cost €

0

EC-Contrib. €

0

Partnership

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 PROGLUTASIS project word cloud

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

follows    strategies    worldwide    source    traits    apportioning    abundant    validate    perspective    dynamics    risk    30    functional    immunometabolic    progression    dampening    appreciation    disorders    glutaminolysis    onset    regulation    usa    ultimately    risks    emerged    intervene    mechanism    health    immunosuppressive    elusive    poorly    cardiovascular    favor    diseases    therapeutic    inflammatory    syndrome    immune    hematopoiesis    atherosclerosis    combination    community    metabolic    proliferative    medical    notion    occurring    despite    diabetes    homeostasis    glutamine    ubiquitous    proglutasis    plasma    origin    contribution    inflammation    alteration    chronic    cells    public    population    disease    acid    mets    reflects    molecular    association    ratio    grade    cardiometabolic    amino    function    underlying    considerable    linking    stress    nutrients    energy    glutamate    hematopoietic    direct    macrophage    trajectory    flexibility    mechanisms    prevalence    obesity   

Project "PROGLUTASIS" data sheet

The following table provides information about the project.

Coordinator
INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE 

Organization address
address: RUE DE TOLBIAC 101
city: PARIS
postcode: 75654
website: www.inserm.fr

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 France [FR]
 Total cost 2˙091˙338 €
 EC max contribution 2˙091˙338 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2016-COG
 Funding Scheme ERC-COG
 Starting year 2017
 Duration (year-month-day) from 2017-04-01   to  2022-03-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE FR (PARIS) coordinator 2˙091˙338.00

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 Project objective

The metabolic syndrome (MetS) represents one of the major public health challenges worldwide. It reflects a combination of medical disorders that, when occurring together, increase the risk of developing diabetes and cardiovascular disease. The prevalence in the USA is estimated at 30% of the population and the European community follows this trajectory. It is now recognized that the state of chronic low-grade inflammation may favor the onset and progression of the MetS. While the notion of metabolic flexibility in hematopoietic cells has recently emerged in several inflammatory diseases, the origin of this immunometabolic alteration in the MetS remains elusive. There is a growing appreciation that the apportioning of nutrients into different metabolic pathways can support or direct functional immune and hematopoietic changes. Glutamine is the most abundant amino acid in the plasma and an important energy source through glutaminolysis. Despite its potential proliferative and/or immunosuppressive function and the strong association between high glutamine-to-glutamate ratio with cardiometabolic traits, the underlying mechanisms are poorly understood. Thus, there is a considerable therapeutic interest in better understanding the mechanisms linking glutamine to cardiometabolic risks and in particular cardiometabolic inflammation. In PROGLUTASIS, we will investigate the metabolic and immune regulation of glutamine homeostasis in the metabolic syndrome. We will validate the contribution of glutaminolysis in cardiometabolic inflammation, including obesity, diabetes and atherosclerosis through its role on hematopoiesis and macrophage dynamics. Given the ubiquitous association between glutamine and chronic metabolic stress, we expect that identifying the underlying molecular mechanism will offer novel therapeutic perspective on how to intervene in this pathway. This will ultimately allow for tailored strategies aimed at dampening cardiometabolic inflammation in the MetS.

 Publications

year authors and title journal last update
List of publications.
2019 Laurent Yvan-Charvet, Johanna Merlin
Le sommeil protège-t-il nos vaisseaux sanguins ?
published pages: 743-746, ISSN: 0767-0974, DOI: 10.1051/medsci/2019147
médecine/sciences 35/10 2019-11-25
2019 Laurent Yvan-Charvet, Fabrizia Bonacina, Rodolphe Renè Guinamard, Giuseppe Danilo Norata
Immunometabolic function of cholesterol in cardiovascular disease and beyond
published pages: 1393-1407, ISSN: 0008-6363, DOI: 10.1093/cvr/cvz127
Cardiovascular Research 115/9 2019-11-25
2019 Stoyan Ivanov, Alexandre Gallerand, Marilyn Gros, Marion I. Stunault, Johanna Merlin, Nathalie Vaillant, Laurent Yvan‐Charvet, Rodolphe R. Guinamard
Mesothelial cell CSF1 sustains peritoneal macrophage proliferation
published pages: 2012-2018, ISSN: 0014-2980, DOI: 10.1002/eji.201948164
European Journal of Immunology 49/11 2019-11-25
2019 Laurent Yvan-Charvet, Lai Guan Ng
Granulopoiesis and Neutrophil Homeostasis: A Metabolic, Daily Balancing Act
published pages: 598-612, ISSN: 1471-4906, DOI: 10.1016/j.it.2019.05.004
Trends in Immunology 40/7 2019-11-25
2018 Laurent Yvan-Charvet, Bertrand Cariou
Poststatin era in atherosclerosis management
published pages: 1, ISSN: 0957-9672, DOI: 10.1097/MOL.0000000000000505
Current Opinion in Lipidology 2019-04-18
2018 Laurent Yvan-Charvet, Filip K Swirski
Is defective cholesterol efflux an integral inflammatory component in myelopoiesis-driven cardiovascular diseases?
published pages: 2168-2171, ISSN: 0195-668X, DOI: 10.1093/eurheartj/ehy269
European Heart Journal 39/23 2019-04-18

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