Opendata, web and dolomites

SkinTrmDeep SIGNED

Tissue Resident Memory (Trm) CD8+ T cells: Genome-wide dissection of cellular differentiation and heterogeneity

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 SkinTrmDeep project word cloud

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

cytokine    immunotherapies    forefront    profiles    framework    circulating    epigenetic    organs    identification    unprecedented    resolution    cell    phenotypically    function    flow    protection    functionally    career    limited    microenvironment    cellular    skin    unravelling    heterogeneity    map    producing    tissue    basis    host    populations    determined    biology    coupled    regulatory    promise    imprinting    throughput    lymphocyte    rely    trm    genome    pathogens    am    young    predominant    immunity    resident    lungs    lymphocytes    residency    shaping    collaborations    functions    memory    localized    lymphoid    cytotoxic    mounting    molecular    tissues    encompassing    ontogeny    denominators    gut    scientist    mechanisms    barrier    immune    binding    unravel    poorly    pathology    population    samples    integral    ultimate    comprising    decipher    sorting    sequencing    goals    rna    human    cells    diverse    understand    differentiation    illuminate    diseases    independent    critical    cd8    surfaces    chromatin    potentially    patient    accessibility    single    eliciting    effector    interactions    generating    cytometry    transcription    multidisciplinary    capacity   

Project "SkinTrmDeep" data sheet

The following table provides information about the project.

Coordinator
KAROLINSKA INSTITUTET 

Organization address
address: Nobels Vag 5
city: STOCKHOLM
postcode: 17177
website: www.ki.se

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 Sweden [SE]
 Total cost 173˙857 €
 EC max contribution 173˙857 € (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-ST
 Starting year 2019
 Duration (year-month-day) from 2019-03-01   to  2021-02-28

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    KAROLINSKA INSTITUTET SE (STOCKHOLM) coordinator 173˙857.00

Map

 Project objective

Tissue-resident memory (Trm) cells are non-circulating T lymphocytes of non-lymphoid tissues and organs that provide localized protection at barrier surfaces such as skin, gut and lungs. In human skin, Trm cells represent the predominant lymphocyte population, comprising subsets with different cytokine profiles and cytotoxic capacity. They represent an integral part of barrier immunity, mounting tailored responses to diverse pathogens, but potentially also eliciting immune pathology. Trm cell differentiation, effector mechanisms and cellular interactions remain poorly defined. I aim to decipher cytotoxic Trm cell biology in greater depth, unravelling the epigenetic framework of phenotypically and functionally distinct CD8 Trm populations. I will rely on state-of-the-art methodologies at the host institution. Through unique collaborations and a multidisciplinary approach encompassing advanced flow cytometry, cell sorting and high-throughput sequencing, I propose to map genome-wide chromatin accessibility in skin and gut Trm cell subsets. Identification of regulatory elements critical for cell functions coupled with analyses of transcription factor binding promise to unravel the molecular mechanisms defining Trm cell ontogeny, function and tissue-specific imprinting. Moreover, with potential application to limited patient samples, single-cell RNA sequencing of cytokine-producing cells will provide a map of Trm cell heterogeneity with unprecedented resolution. This project will illuminate the role of the microenvironment in shaping tissue-resident memory, with ultimate goals to understand Trm cell-related diseases and determine common denominators required to establish tissue residency and provide basis for generating and shaping Trm cells in future cellular immunotherapies. Being at the forefront of the research on the epigenetic differentiation processes of lymphocytes, I am determined to build a strong basis for a future career as a young independent scientist.

Are you the coordinator (or a participant) of this project? Plaese send me more information about the "SKINTRMDEEP" project.

For instance: the website url (it has not provided by EU-opendata yet), the logo, a more detailed description of the project (in plain text as a rtf file or a word file), some pictures (as picture files, not embedded into any word file), twitter account, linkedin page, etc.

Send me an  email (fabio@fabiodisconzi.com) and I put them in your project's page as son as possible.

Thanks. And then put a link of this page into your project's website.

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

More projects from the same programme (H2020-EU.1.3.2.)

BiMetaCat (2019)

Two Are Better Than One: Bimetallic Catalysts for the Conversion of Lignin-Derived Aryl-Ethers

Read More  

ItalianWoolf (2019)

Virginia Woolf and Italian Readers

Read More  

LYSOKIN (2020)

Architecture and regulation of PI3KC2β lipid kinase complex for nutrient signaling at the lysosome

Read More