Draxin from neocortical neurons controls the guidance of thalamocortical projections into the neocortex

The thalamocortical tract carries sensory information to the neocortex. It has long been recognized that the neocortical pioneer axons of subplate neurons are essential for thalamocortical development. Herein we report that an axon guidance cue, draxin, is expressed in early-born neocortical neurons...

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Veröffentlicht in:Nature communications 2015-12, Vol.6 (1), p.10232-10232, Article 10232
Hauptverfasser: Shinmyo, Yohei, Asrafuzzaman Riyadh, M., Ahmed, Giasuddin, Bin Naser, Iftekhar, Hossain, Mahmud, Takebayashi, Hirohide, Kawasaki, Hiroshi, Ohta, Kunimasa, Tanaka, Hideaki
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Sprache:eng
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Zusammenfassung:The thalamocortical tract carries sensory information to the neocortex. It has long been recognized that the neocortical pioneer axons of subplate neurons are essential for thalamocortical development. Herein we report that an axon guidance cue, draxin, is expressed in early-born neocortical neurons, including subplate neurons, and is necessary for thalamocortical development. In draxin −/− mice, thalamocortical axons do not enter the neocortex. This phenotype is sufficiently rescued by the transgenic expression of draxin in neocortical neurons. Genetic interaction data suggest that draxin acts through Deleted in colorectal cancer (DCC) and Neogenin (Neo1), to regulate thalamocortical projections in vivo . Draxin promotes the outgrowth of thalamic axons in vitro and this effect is abolished in thalamic neurons from Dcc and Neo1 double mutants. These results suggest that draxin from neocortical neurons controls thalamocortical projections into the neocortex, and that this effect is mediated through the DCC and Neo1 receptors. During neural development thalamocortical axons follow corticofugal projections into the neocortex. Here, using a combination of knock down and rescue experiments, the authors show that Draxin expression in neocortical cells promotes thalamic axon projections from the internal capsule.
ISSN:2041-1723
2041-1723
DOI:10.1038/ncomms10232