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Contralateral migration of oculomotor neurons is regulated by Slit/Robo signaling

BACKGROUND: Oculomotor neurons develop initially like typical motor neurons, projecting axons out of the ventral midbrain to their ipsilateral targets, the extraocular muscles. However, in all vertebrates, after the oculomotor nerve (nIII) has reached the extraocular muscle primordia, the cell bodie...

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Autores principales: Bjorke, Brielle, Shoja-Taheri, Farnaz, Kim, Minkyung, Robinson, G. Eric, Fontelonga, Tatiana, Kim, Kyung-Tai, Song, Mi-Ryoung, Mastick, Grant S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5075191/
https://www.ncbi.nlm.nih.gov/pubmed/27770832
http://dx.doi.org/10.1186/s13064-016-0073-y
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author Bjorke, Brielle
Shoja-Taheri, Farnaz
Kim, Minkyung
Robinson, G. Eric
Fontelonga, Tatiana
Kim, Kyung-Tai
Song, Mi-Ryoung
Mastick, Grant S.
author_facet Bjorke, Brielle
Shoja-Taheri, Farnaz
Kim, Minkyung
Robinson, G. Eric
Fontelonga, Tatiana
Kim, Kyung-Tai
Song, Mi-Ryoung
Mastick, Grant S.
author_sort Bjorke, Brielle
collection PubMed
description BACKGROUND: Oculomotor neurons develop initially like typical motor neurons, projecting axons out of the ventral midbrain to their ipsilateral targets, the extraocular muscles. However, in all vertebrates, after the oculomotor nerve (nIII) has reached the extraocular muscle primordia, the cell bodies that innervate the superior rectus migrate to join the contralateral nucleus. This motor neuron migration represents a unique strategy to form a contralateral motor projection. Whether migration is guided by diffusible cues remains unknown. METHODS: We examined the role of Slit chemorepellent signals in contralateral oculomotor migration by analyzing mutant mouse embryos. RESULTS: We found that the ventral midbrain expresses high levels of both Slit1 and 2, and that oculomotor neurons express the repellent Slit receptors Robo1 and Robo2. Therefore, Slit signals are in a position to influence the migration of oculomotor neurons. In Slit 1/2 or Robo1/2 double mutant embryos, motor neuron cell bodies migrated into the ventral midbrain on E10.5, three days prior to normal migration. These early migrating neurons had leading projections into and across the floor plate. In contrast to the double mutants, embryos which were mutant for single Slit or Robo genes did not have premature migration or outgrowth on E10.5, demonstrating a cooperative requirement of Slit1 and 2, as well as Robo1 and 2. To test how Slit/Robo midline repulsion is modulated, we found that the normal migration did not require the receptors Robo3 and CXCR4, or the chemoattractant, Netrin 1. The signal to initiate contralateral migration is likely autonomous to the midbrain because oculomotor neurons migrate in embryos that lack either nerve outgrowth or extraocular muscles, or in cultured midbrains that lacked peripheral tissue. CONCLUSION: Overall, our results demonstrate that a migratory subset of motor neurons respond to floor plate-derived Slit repulsion to properly control the timing of contralateral migration.
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spelling pubmed-50751912016-10-27 Contralateral migration of oculomotor neurons is regulated by Slit/Robo signaling Bjorke, Brielle Shoja-Taheri, Farnaz Kim, Minkyung Robinson, G. Eric Fontelonga, Tatiana Kim, Kyung-Tai Song, Mi-Ryoung Mastick, Grant S. Neural Dev Research Article BACKGROUND: Oculomotor neurons develop initially like typical motor neurons, projecting axons out of the ventral midbrain to their ipsilateral targets, the extraocular muscles. However, in all vertebrates, after the oculomotor nerve (nIII) has reached the extraocular muscle primordia, the cell bodies that innervate the superior rectus migrate to join the contralateral nucleus. This motor neuron migration represents a unique strategy to form a contralateral motor projection. Whether migration is guided by diffusible cues remains unknown. METHODS: We examined the role of Slit chemorepellent signals in contralateral oculomotor migration by analyzing mutant mouse embryos. RESULTS: We found that the ventral midbrain expresses high levels of both Slit1 and 2, and that oculomotor neurons express the repellent Slit receptors Robo1 and Robo2. Therefore, Slit signals are in a position to influence the migration of oculomotor neurons. In Slit 1/2 or Robo1/2 double mutant embryos, motor neuron cell bodies migrated into the ventral midbrain on E10.5, three days prior to normal migration. These early migrating neurons had leading projections into and across the floor plate. In contrast to the double mutants, embryos which were mutant for single Slit or Robo genes did not have premature migration or outgrowth on E10.5, demonstrating a cooperative requirement of Slit1 and 2, as well as Robo1 and 2. To test how Slit/Robo midline repulsion is modulated, we found that the normal migration did not require the receptors Robo3 and CXCR4, or the chemoattractant, Netrin 1. The signal to initiate contralateral migration is likely autonomous to the midbrain because oculomotor neurons migrate in embryos that lack either nerve outgrowth or extraocular muscles, or in cultured midbrains that lacked peripheral tissue. CONCLUSION: Overall, our results demonstrate that a migratory subset of motor neurons respond to floor plate-derived Slit repulsion to properly control the timing of contralateral migration. BioMed Central 2016-10-22 /pmc/articles/PMC5075191/ /pubmed/27770832 http://dx.doi.org/10.1186/s13064-016-0073-y Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Bjorke, Brielle
Shoja-Taheri, Farnaz
Kim, Minkyung
Robinson, G. Eric
Fontelonga, Tatiana
Kim, Kyung-Tai
Song, Mi-Ryoung
Mastick, Grant S.
Contralateral migration of oculomotor neurons is regulated by Slit/Robo signaling
title Contralateral migration of oculomotor neurons is regulated by Slit/Robo signaling
title_full Contralateral migration of oculomotor neurons is regulated by Slit/Robo signaling
title_fullStr Contralateral migration of oculomotor neurons is regulated by Slit/Robo signaling
title_full_unstemmed Contralateral migration of oculomotor neurons is regulated by Slit/Robo signaling
title_short Contralateral migration of oculomotor neurons is regulated by Slit/Robo signaling
title_sort contralateral migration of oculomotor neurons is regulated by slit/robo signaling
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5075191/
https://www.ncbi.nlm.nih.gov/pubmed/27770832
http://dx.doi.org/10.1186/s13064-016-0073-y
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