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PlastiCell SIGNED

Using a natural cellular plasticity event to decypher the cellular requirements and molecular circuitry promoting transdifferentiation at the single cell level.

Total Cost €

0

EC-Contrib. €

0

Partnership

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 PlastiCell project word cloud

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

species    molecular    ease    acquire    experimentally    nuclear    tremendous    underlie    initiation    neighbours    mice    reprograming    phyla    identical    functionally    demonstration    natural    perception    events    identities    question    occur    developmental    efficiency    revealed    elucidate    architecture    reprogramming    identity    fascinating    permissive    aka    cancerous    unambiguous    influence    conserved    cellular    apparently    how    cells    single    systematically    first    push    provides    event    100    regenerative    types    cell    followed    transdifferentiation    complexes    relative    motoneuron    demonstrated    naturally    act    circuitry    reprogrammed    mechanisms    frontiers    conversion    model    predictable    td    network    interconversions    questions    brake    context    avenues    protect    vivo    counteracted    efficient    raises    somatic    discrete    asset    jellyfish    medicine    elegans    tackles    impressive    reported    diverse    rectal    plasticity    networks    differentiated    unravel   

Project "PlastiCell" data sheet

The following table provides information about the project.

Coordinator
CENTRE EUROPEEN DE RECHERCHE EN BIOLOGIE ET MEDECINE 

Organization address
address: Rue Laurent Fries 1
city: ILLKIRCH GRAFFENSTADEN
postcode: 67404
website: www.igbmc.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]
 Project website http://www.igbmc.fr/research/department/1/team/8/
 Total cost 2˙000˙000 €
 EC max contribution 2˙000˙000 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2014-CoG
 Funding Scheme ERC-COG
 Starting year 2015
 Duration (year-month-day) from 2015-07-01   to  2021-06-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    CENTRE EUROPEEN DE RECHERCHE EN BIOLOGIE ET MEDECINE FR (ILLKIRCH GRAFFENSTADEN) coordinator 2˙000˙000.00

Map

 Project objective

How differentiated cells can change their identity is a fascinating question. Indeed, natural interconversions between functionally distinct somatic cell types (aka transdifferentiation, Td) have been reported in species as diverse as jellyfish and mice, while experimentally induced reprogramming of differentiated cells has been demonstrated. The relative ease with which cellular identities can be reprogrammed raises a number of exciting questions: What mechanisms and steps allow a given cell, but not its apparently identical neighbours, to naturally acquire a new plasticity potential and change its identity? How does the cellular context influence the ability of a cell to be reprogrammed? What cellular mechanisms must be counteracted to allow natural reprograming to occur? What circuitry underlie the impressive efficiency observed in natural events? The proposed project tackles these questions To systematically identify the molecular networks and cellular requirements of Td, we established a simple model of natural Td, in C. elegans, where the conversion of a rectal cell into a motoneuron is followed in vivo. This model is unique: it is 100% efficient, predictable and provides the first unambiguous demonstration, at the single cell level, of natural Td. The study of such natural event has revealed a key asset to unravel the discrete steps of the process, their control and the conserved cell plasticity factors promoting its initiation, while leading to important concepts conserved across phyla. We propose here 4 aims to push new frontiers and: i) Define what makes a cellular context permissive; ii) Elucidate the conserved nuclear complexes and network architecture promoting efficient reprogramming; iii) Identify mechanisms that protect the differentiated identity and act as a brake to Td. Understanding cell plasticity in vivo will have a tremendous impact on our perception of developmental and cancerous processes and could open new avenues for regenerative medicine.

 Publications

year authors and title journal last update
List of publications.
2016 M. Doitsidou, S. Jarriault, R. J. Poole
Next-Generation Sequencing-Based Approaches for Mutation Mapping and Identification in Caenorhabditis elegans
published pages: 451-474, ISSN: 0016-6731, DOI: 10.1534/genetics.115.186197
Genetics 204/2 2019-11-14
2017 Magdalena Götz, Sophie Jarriault
Programming and reprogramming the brain: a meeting of minds in neural fate
published pages: 2714-2718, ISSN: 0950-1991, DOI: 10.1242/dev.150466
Development 144/15 2019-11-14
2016 Sarah F. Becker, Sophie Jarriault
Natural and induced direct reprogramming: mechanisms, concepts and general principles — from the worm to vertebrates
published pages: 154-163, ISSN: 0959-437X, DOI: 10.1016/j.gde.2016.06.014
Current Opinion in Genetics and Development 40 2019-11-14
2018 Laura Vibert, Anne Daulny, Sophie Jarriault
Wound healing, cellular regeneration and plasticity: the elegans way
published pages: 491-505, ISSN: 0214-6282, DOI: 10.1387/ijdb.180123sj
The International Journal of Developmental Biology 62/6-7-8 2019-11-14

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