FLRT IN NEUROBIOLOGY

Genetic analysis of a novel family of repulsive guidance cues acting through Unc5 receptors

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

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

contact info
Titolo: Ms.
Nome: Annette
Cognome: Starke
Email: send email
Telefono: +49 89 85783776

 Nazionalità Coordinatore Germany [DE]
 Totale costo 162˙742 €
 EC contributo 162˙742 €
 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-2010-IEF
 Funding Scheme MC-IEF
 Anno di inizio 2012
 Periodo (anno-mese-giorno) 2012-06-01   -   2014-05-31

 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: Ms.
Nome: Annette
Cognome: Starke
Email: send email
Telefono: +49 89 85783776

DE (MUENCHEN) coordinator 162˙742.40

Mappa


 Word cloud

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

dr    unc    guidance    cues    neurons    axon    connections    shed    functional    nerve    receptors    light    signaling    cell    mice    nervous    molecular    neurobiology    fellow    mouse    mutant    migration    flrts    correct    flrt    klein    proteins    assays   

 Obiettivo del progetto (Objective)

'One of the most challenging problems in neurobiology is to understand the mechanisms that mediate the formation of a functional neuronal network. Despite the identification of several molecules that regulate axon guidance and cell migration, it is unclear how these factors can specify a large number of connections in the nervous system. The present project aims to study the role and mechanism of action of the Fibronectin Leucine-Rich Transmembrane (FLRT) family protein in axon guidance and cell migration during mouse central nervous system (CNS) development. The proposed fellow intends to tackle this problem using a multidisciplinary approach including conditional mouse mutant mice lacking either specific FLRT or Unc5 proteins, cell based functional assays using neurons derived from mutant mice, and molecular and biochemical assays to identify signalling pathways activated by FLRTs. Recent unpublished results from the proposed host institution, the Department of Molecular Neurobiology (Dr. Klein) at Max Planck Institute of Neurobiology, indicate that shed ectodomains of FLRTs can function as long-range guidance cues for cortical neurons in vitro and in vivo. FLRTs exert their functions by binding to Unc5 receptors. Moreover, FLRTs may also act as cell autonomous signaling receptors. Thus, FLRT proteins have the potential to engage in bi-directional signaling (‘forward’ via Unc5 receptors and ‘reverse’ via their own intracellular domain), an original and innovative concept which Dr. Klein previously pioneered in the ephrin/Eph field. Should the hypothesis of the proposed research be correct, the findings will undoubtedly represent an advance in the state of art in the neurobiology area, and also may shed light on certain neural developmental disorders. The proposed fellow will highly benefit from the challenging research environment and supervision of a renowned scientist, which will offer him promising perspectives for his further research career in Europe.'

Introduzione (Teaser)

EU-funded research has investigated the genetic basis behind formation of precise and specific nerve cell connections during embryo development. Crucial for a fully functioning nervous system, the work has shed light on guidance cues that help to orchestrate billions of nerve cells into the correct positions.

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