Celsr3 is required in motor neurons to steer their axons in the hindlimb

In this study, the authors show that Celsr3 and Fzd3 interact in motor neurons to cooperatively direct axon guidance to target muscles in the periphery. In addition, they find that loss of Celsr3 or Fzd3 function also impairs axonal responses to ephrinA reverse, attractive signaling, suggesting a fu...

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Veröffentlicht in:Nature neuroscience 2014-09, Vol.17 (9), p.1171-1179
Hauptverfasser: Chai, Guoliang, Zhou, Libing, Manto, Mario, Helmbacher, Françoise, Clotman, Frédéric, Goffinet, André M, Tissir, Fadel
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Sprache:eng
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Zusammenfassung:In this study, the authors show that Celsr3 and Fzd3 interact in motor neurons to cooperatively direct axon guidance to target muscles in the periphery. In addition, they find that loss of Celsr3 or Fzd3 function also impairs axonal responses to ephrinA reverse, attractive signaling, suggesting a functional interaction between these guidance pathways. The cadherin Celsr3 regulates the directional growth and targeting of axons in the CNS, but whether it acts in collaboration with or in parallel to other guidance cues is unknown. Furthermore, the function of Celsr3 in the peripheral nervous system is still largely unexplored. Here we show that Celsr3 mediates pathfinding of motor axons innervating the hindlimb. In mice, Celsr3-deficient axons of the peroneal nerve segregate from those of the tibial nerve but fail to extend dorsally, and they stall near the branch point. Mutant axons respond to repulsive ephrinA-EphA forward signaling and glial cell–derived neurotrophic factor (GDNF). However, they are insensitive to attractive EphA-ephrinA reverse signaling. In transfected cells, Celsr3 immunoprecipitates with ephrinA2, ephrinA5, Ret, GDNF family receptor α1 (GFRα1) and Frizzled3 (Fzd3). The function of Celsr3 is Fzd3 dependent but Vangl2 independent. Our results provide evidence that the Celsr3-Fzd3 pathway interacts with EphA-ephrinA reverse signaling to guide motor axons in the hindlimb.
ISSN:1097-6256
1546-1726
DOI:10.1038/nn.3784