REGENERATEACROSS

A Cross Species Approach to Understand the Mechanism and Evolution of Limb Regeneration Capacity

 Coordinatore TECHNISCHE UNIVERSITAET DRESDEN 

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 Nazionalità Coordinatore Germany [DE]
 Totale costo 2˙447˙600 €
 EC contributo 2˙447˙600 €
 Programma FP7-IDEAS-ERC
Specific programme: "Ideas" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call ERC-2011-ADG_20110310
 Funding Scheme ERC-AG
 Anno di inizio 2012
 Periodo (anno-mese-giorno) 2012-06-01   -   2017-05-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    TECHNISCHE UNIVERSITAET DRESDEN

 Organization address address: HELMHOLTZSTRASSE 10
city: DRESDEN
postcode: 1069

contact info
Titolo: Ms.
Nome: Friederieke
Cognome: Noack
Email: send email
Telefono: +49 351 463 42191
Fax: +49 351 463 39742

DE (DRESDEN) hostInstitution 2˙447˙600.00
2    TECHNISCHE UNIVERSITAET DRESDEN

 Organization address address: HELMHOLTZSTRASSE 10
city: DRESDEN
postcode: 1069

contact info
Titolo: Prof.
Nome: Elly Margaret
Cognome: Tanaka
Email: send email
Telefono: +49 351 458 82000
Fax: +49 351 458 82009

DE (DRESDEN) hostInstitution 2˙447˙600.00

Mappa


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perform    cues    regeneration    extracellular    connective    healing    regenerative    progenitors    tip    mouse    salamander    versus    intrinsic    tissue    cell    profiling    patterned    molecular    cells    frog    expression    limb    wound    lineage    determine    finger    differences    cellular    fibroblast   

 Obiettivo del progetto (Objective)

'Limb regeneration capacity varies among vertebrates, ranging from full regeneration in salamanders, to stage-restricted premetamorphic regeneration in frogs, to finger-tip regeneration in newborn mice and humans. The molecular and cellular basis for these differences in regeneration ability is not known and it is still unclear if these different regenerative events are tied by some common mechanisms with progressive restriction due to extracellular signals or cell intrinsic changes. Connective tissue fibroblasts or their progenitors play a key role in regenerating the patterned salamander limb. They harbor critical positional information and can reconstitute not only the connective tissue but also a complete, patterned skeleton. In contrast, such cells typically contribute to scar tissue during mammalian wound healing. Their role in mouse finger tip regeneration is unknown. I seek to determine the differences in fibroblast biology that account for the differences in regeneration between salamander, frog and mouse. To define the differences in composition of the connective tissue population, I will perform parallel lineage tracing of different fibroblast populations and their progenitors during wound healing and regeneration in salamander, frog and mouse. To determine differences in cell intrinsic potential versus extracellular cues required for regeneration I will perform cross-species transplantation of lineage-labeled cells between salamander and frog coupled with expression profiling to identify molecular changes that occur in cells in a regenerative versus non-regenerative context. Finally I will use this expression profiling and our molecular knowledge of limb regeneration factors to test whether frog and mouse cells can acquire regenerative traits at the cellular level by the forced exposure to intracellular and extracellular regeneration cues or by the downregulation of putative inhibitory factors.'

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