REGENERATION

The role of neuronal progenitor cells in axolotl spinal cord regeneration

 Coordinatore MAX PLANCK GESELLSCHAFT ZUR FOERDERUNG DER WISSENSCHAFTEN E.V. 

 Organization address address: Hofgartenstrasse 8
city: MUENCHEN
postcode: 80539

contact info
Titolo: Dr.
Nome: Birgit
Cognome: Knepper-Nicolai
Email: send email
Telefono: -2103074
Fax: -2101391

 Nazionalità Coordinatore Germany [DE]
 Totale costo 168˙116 €
 EC contributo 168˙116 €
 Programma FP7-PEOPLE
Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call FP7-PEOPLE-2007-4-2-IIF
 Funding Scheme MC-IIF
 Anno di inizio 2008
 Periodo (anno-mese-giorno) 2008-07-01   -   2010-06-30

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    MAX PLANCK GESELLSCHAFT ZUR FOERDERUNG DER WISSENSCHAFTEN E.V.

 Organization address address: Hofgartenstrasse 8
city: MUENCHEN
postcode: 80539

contact info
Titolo: Dr.
Nome: Birgit
Cognome: Knepper-Nicolai
Email: send email
Telefono: -2103074
Fax: -2101391

DE (MUENCHEN) coordinator 0.00

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 Word cloud

Esplora la "nuvola delle parole (Word Cloud) per avere un'idea di massima del progetto.

progenitor    mature    determine    me    spinal    expression    helix    tissue    fate    regeneration    population    committed    cells    regenerate    neurons    bhlh    proteins    neuronal    axolotl    cord    expressing    progenitors    derive    experiments   

 Obiettivo del progetto (Objective)

'During spinal cord regeneration in the axolotl, it has been shown that all of the neurons in the regenerate derive from cells near the site of amputation. It is unknown whether the new neurons derive from a population of multipotent progenitor cells in the mature tissue, or whether committed neuronal progenitors also contribute. Focusing on committed neuronal progenitors expressing the basic helix-loop-helix (bHLH) family of proneural transcription factors, I will identify the expression patterns of these proteins in the developing, mature, and regenerating spinal cord and determine whether a population of committed neural progenitors persists in the adult axolotl tissue. Using a Cre/loxP reporter system to permanently label bHLH-expressing cells, I will track the fates of these cells during normal development and regeneration. This technique will also allow me to determine whether spinal cord regeneration involves de-differentiation of committed neuronal progenitors to a more embryonic-like state. Transplantation of labeled cells will allow me to determine whether positional cues direct the fate of a committed progenitor, or whether expression of specific bHLH proteins is itself enough to determine the fate of the cell. These experiments will provide a foundation for future experiments to identify the signaling molecules that induce progenitor cells to proliferate and regenerate the spinal cord after injury.'

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