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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 €

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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.

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

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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