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  GDNF acts as a chemoattractant to support ephrinA-induced repulsion of limb motor axons

Dudanova, I., Gatto, G., & Klein, R. (2010). GDNF acts as a chemoattractant to support ephrinA-induced repulsion of limb motor axons. Current Biology, 20(23), 2150-2156. doi:10.1016/j.cub.2010.11.021.

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Dudanova, I.1, Author           
Gatto, G.1, Author           
Klein, R.1, Author           
Affiliations:
1Department: Molecular Neurobiology / Klein, MPI of Neurobiology, Max Planck Society, ou_1113546              

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 Abstract: Despite the abundance of guidance cues in vertebrate nervous systems, little is known about cooperation between them [1-3]. Motor axons of the lateral motor column (LMCL) [4, 5] require two ligand/receptor systems, ephrinA/EphA4 and glial cell line-derived neurotrophic factor (GDNF)/Ret, to project to the dorsal limb [6-8]. Deletion of either EphA4 or Ref in mice leads to rerouting of a portion of LMCL axons to the ventral limb, a phenotype enhanced in EphA4;Ret double mutants [7, 8]. The guidance errors in EphA4 knockouts were attributed to the lack of repulsion from ephrinAs in the ventral mesenchyme [6, 7, 9]. However, it has remained unclear how GDNF, expressed dorsally next to the choice point [8], acts on motor axons and cooperates with ephrinAs. Here we show that GDNF induces attractive turning of LMCL axons. When presented in countergradients, GDNF and ephrinAs cooperate in axon turning, indicating that the receptors Ret and EphA4 invoke opposite effects within the same growth cone. GDNF also acts in a permissive manner by reducing ephrinA-induced collapse and keeping the axons in a growth-competent state. This is the first example of two opposing cues promoting the same trajectory choice at an intermediate target.

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Language(s): eng - English
 Dates: 2010-11-25
 Publication Status: Issued
 Pages: -
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 Table of Contents: -
 Rev. Type: Peer
 Identifiers: eDoc: 522621
ISI: 000285213500031
DOI: 10.1016/j.cub.2010.11.021
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Title: Current Biology
  Abbreviation : Curr. Biol.
Source Genre: Journal
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Publ. Info: London, UK : Cell Press
Pages: - Volume / Issue: 20 (23) Sequence Number: - Start / End Page: 2150 - 2156 Identifier: ISSN: 0960-9822
CoNE: https://pure.mpg.de/cone/journals/resource/954925579107