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PIOMES

Pbx proteins as pioneer factors promoting signal specificity in mesodermal differentiation

Total Cost €

0

EC-Contrib. €

0

Partnership

0

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0

 PIOMES project word cloud

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

routinely    question    muscular    lineage    life    human    shape    dystrophies    region    progenitors    somitic    central    date    genetic    tools    converting    murine    combines    specify    analogous    opening    extensively    strength    acquisition    promotes    stem    chromatin    treating    vitro    mouse    rational    danstem    degenerative    epiblast    strategies    differentiation    blood    recruitment    transcriptional    expressed    training    insights    cell    pbx    embryos    hescs    ways    cellular    assays    streak    skeletal    cells    binding    specified    proteins    mps    regulation    specification    limited    signalling    mesodermal    mastered    transcription    diseases    types    purpose    embryo    pioneer    efficiency    bone    healthy    fate    postdoctoral    dynamics    ultimately    mesoderm    arise    tf    had    esc    pools    wnt    muscles    regenerative    organisms    embryonic    muscle    landscape    tfs    critical    primitive    combat    competence    immunoprecipitation    conceive   

Project "PIOMES" data sheet

The following table provides information about the project.

Coordinator
KOBENHAVNS UNIVERSITET 

Organization address
address: NORREGADE 10
city: KOBENHAVN
postcode: 1165
website: www.ku.dk

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 Denmark [DK]
 Project website http://danstem.ku.dk/research1/ferretti-lab/
 Total cost 200˙194 €
 EC max contribution 200˙194 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2014
 Funding Scheme MSCA-IF-EF-RI
 Starting year 2015
 Duration (year-month-day) from 2015-05-01   to  2017-04-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    KOBENHAVNS UNIVERSITET DK (KOBENHAVN) coordinator 200˙194.00

Map

 Project objective

The development of healthy organisms requires the formation of different cellular systems, such as a blood, bone and muscle. All these different cell types arise during embryonic life from specific pools of mesodermal progenitors (MPs). A central question is how distinct MPs are specified and ultimately why different cells respond to signalling pathways in different ways? Critical insights here are directly relevant to conceive strategies for increasing the efficiency of mesodermal differentiation aimed for treating muscular degenerative diseases. To date, in vitro, somitic mesoderm differentiation for regenerative purpose has had limited success. Wnt signalling promotes Embryonic Stem Cell (ESC) differentiation of all the MPs, including skeletal muscles. The activity of specific pioneer transcription factors (TFs) may be the key for converting Wnt signalling pathways into a specific transcriptional program. Pioneer TFs shape the chromatin landscape by opening the chromatin and allowing the recruitment of lineage specific TFs, and thus ultimately control the TF binding dynamics and the acquisition of a specific cell fate. Pbx proteins are pioneer TFs, which are specifically expressed in the primitive streak, the region of the embryo that will produce all mesoderm, and are critical for promoting mesodermal specification. Here, I will establish how Pbx proteins specify MPs and determine the competence of early mesoderm to respond to Wnt signalling. To this end, I will use mouse embryos and murine epiblast stem cells, which are analogous to human ESC (hESCs). My approach combines the strength of an in vitro ESC differentiation method, routinely used at DanStem, with chromatin immunoprecipitation and transcriptional regulation assays, which I have extensively mastered during my postdoctoral training. I expect that my findings will provide novel tools for rational design of strategies to combat genetic and degenerative muscular diseases, such as muscular dystrophies.

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

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