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  Met signaling is required for recruitment of motor neurons to PEA3-positive motor pools

Helmbacher, F., Dessaud, E., Arber, S., deLapeyriere, O., Henderson, C., Klein, R., et al. (2003). Met signaling is required for recruitment of motor neurons to PEA3-positive motor pools. Neuron, 39(5), 767-777. doi:10.1016/S0896-6273(03)00493-8.

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Helmbacher, Francoise1, Author           
Dessaud, Eric2, Author
Arber, Silvia2, Author
deLapeyriere, Odile2, Author
Henderson, Christopher2, Author
Klein, Rüdiger1, Author           
Maina, Flavio2, Author
Affiliations:
1Department: Molecular Neurobiology / Klein, MPI of Neurobiology, Max Planck Society, ou_1113546              
2Division of Cell Biology, Biozentrum, University of Basel, Klingelbergstrasse 50/70, CH-4056 Basel, Switzerland INSERM U382 IBDM, Université de la Méditerranée - Faculté des Sciences de Luminy, Marseille, France, ou_persistent22              

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 Abstract: Motor neurons in the spinal cord are grouped into motor pools, each of which innervates a single muscle. The ETS transcription factor PEA3 is a marker of a few such motor pools. Here, we show that pea3 is first induced by GDNF in a caudal subset of the motor neurons that will constitute the pea3+ population. Expansion of the pea3 domain subsequently occurs by recruitment of neurons from more anterior segments. Signaling by Met, the HGF receptor, is required for the rostral expansion of the pea3 domain, while the onset of pea3 expression is independent of met function. met expression is observed in pioneer neurons but does not precede that of pea3 in recruited neurons. We provide genetic evidence for a non-cell-autonomous function of met during the recruitment process. We propose the presence of a relay mechanism allowing cells induced by peripheral signals to recruit more anterior neurons to adopt the same motor pool-related phenotype.

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 Dates: 2003-08-28
 Publication Status: Issued
 Pages: -
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 Rev. Type: Peer
 Identifiers: eDoc: 126248
DOI: 10.1016/S0896-6273(03)00493-8
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Title: Neuron
Source Genre: Journal
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Publ. Info: Cambridge, Mass. : Cell Press
Pages: - Volume / Issue: 39 (5) Sequence Number: - Start / End Page: 767 - 777 Identifier: ISSN: 0896-6273
CoNE: https://pure.mpg.de/cone/journals/resource/954925560565