Netrin1-DCC-Mediated Attraction Guides Post-Crossing Commissural Axons in the Hindbrain

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Authors

Shoja-Taheri, Farnaz
DeMarco, Arielle
Mastick, Grant S.

Issue Date

2015

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Article

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Robo , Slit , commissural axon , Netrin , axon guidance , dcc , slit

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Abstract

Commissural axons grow along precise trajectories that are guided by several cues secreted from the ventral midline. After initial attraction to the floor plate using Netrin1 activation of its main attractive receptor, DCC (deleted in colorectal cancer), axons cross the ventral midline, and many turn to grow longitudinally on the contralateral side. After crossing the midline, axons are thought to lose their responsiveness to Netrin1 and become sensitive to midline Slit-Robo repulsion. We aimed to address the in vivo significance of Netrin1 in guiding post-crossing axon trajectories in mouse embryos. Surprisingly, in contrast to the spinal cord, Netrin1 and DCC mutants had abundant commissural axons crossing in the hindbrain. In Netrin1 and DCC mutants, many post-crossing axons made normal turns to grow longitudinally, but projected abnormally at angles away from the midline. In addition, exposure of cultured hindbrain explants to ectopic Netrin1 caused attractive deflection of post-crossing axons. Thus, Netrin1-DCC signaling is not required to attract pre-crossing axons toward the hindbrain floor plate, but is active in post-crossing guidance. Also in contrast with spinal cord, analysis of hindbrain post-crossing axons in Robo1/2 mutant embryos showed that Slit-Robo repulsive signaling was not required for post-crossing trajectories. Our findings show that Netrin1-DCC attractive signaling, but not Slit-Robo repulsive signaling, remains active in hindbrain post-crossing commissural axons to guide longitudinal trajectories, suggesting surprising regional diversity in commissural axon guidance mechanisms.

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Shoja-Taheri, F., DeMarco, A., & Mastick, G. S. (2015). Netrin1-DCC-Mediated Attraction Guides Post-Crossing Commissural Axons in the Hindbrain. The Journal of Neuroscience, 35(33), 11707�"11718. doi:10.1523/jneurosci.0613-15.2015

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Creative Commons Attribution 4.0 International

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0270-6474

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