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Semaphorin-6A controls guidance of corticospinal tract axons at multiple choice points

BACKGROUND: The trajectory of corticospinal tract (CST) axons from cortex to spinal cord involves a succession of choice points, each of which is controlled by multiple guidance molecules. To assess the involvement of transmembrane semaphorins and their plexin receptors in the guidance of CST axons,...

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Autores principales: Rünker, Annette E, Little, Graham E, Suto, Fumikazu, Fujisawa, Hajime, Mitchell, Kevin J
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2647909/
https://www.ncbi.nlm.nih.gov/pubmed/19063725
http://dx.doi.org/10.1186/1749-8104-3-34
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author Rünker, Annette E
Little, Graham E
Suto, Fumikazu
Fujisawa, Hajime
Mitchell, Kevin J
author_facet Rünker, Annette E
Little, Graham E
Suto, Fumikazu
Fujisawa, Hajime
Mitchell, Kevin J
author_sort Rünker, Annette E
collection PubMed
description BACKGROUND: The trajectory of corticospinal tract (CST) axons from cortex to spinal cord involves a succession of choice points, each of which is controlled by multiple guidance molecules. To assess the involvement of transmembrane semaphorins and their plexin receptors in the guidance of CST axons, we have examined this tract in mutants of Semaphorin-6A (Sema6A), Plexin-A2 (PlxnA2) and Plexin-A4 (PlxnA4). RESULTS: We describe defects in CST guidance in Sema6A mutants at choice points at the mid-hindbrain boundary (MHB) and in navigation through the pons that dramatically affect how many axons arrive to the hindbrain and spinal cord and result in hypoplasia of the CST. We also observe defects in guidance within the hindbrain where a proportion of axons aberrantly adopt a ventrolateral position and fail to decussate. This function in the hindbrain seems to be mediated by the known Sema6A receptor PlxnA4, which is expressed by CST axons. Guidance at the MHB, however, appears independent of this and of the other known receptor, PlxnA2, and may depend instead on Sema6A expression on CST axons themselves at embryonic stages. CONCLUSION: These data identify Sema6A as a major contributor to the guidance of CST axons at multiple choice points. They highlight the active control of guidance at the MHB and also implicate the inferior olive as an important structure in the guidance of CST axons within the hindbrain. They also suggest that Sema6A, which is strongly expressed by oligodendrocytes, may affect CST regeneration in adults.
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spelling pubmed-26479092009-02-26 Semaphorin-6A controls guidance of corticospinal tract axons at multiple choice points Rünker, Annette E Little, Graham E Suto, Fumikazu Fujisawa, Hajime Mitchell, Kevin J Neural Dev Research Article BACKGROUND: The trajectory of corticospinal tract (CST) axons from cortex to spinal cord involves a succession of choice points, each of which is controlled by multiple guidance molecules. To assess the involvement of transmembrane semaphorins and their plexin receptors in the guidance of CST axons, we have examined this tract in mutants of Semaphorin-6A (Sema6A), Plexin-A2 (PlxnA2) and Plexin-A4 (PlxnA4). RESULTS: We describe defects in CST guidance in Sema6A mutants at choice points at the mid-hindbrain boundary (MHB) and in navigation through the pons that dramatically affect how many axons arrive to the hindbrain and spinal cord and result in hypoplasia of the CST. We also observe defects in guidance within the hindbrain where a proportion of axons aberrantly adopt a ventrolateral position and fail to decussate. This function in the hindbrain seems to be mediated by the known Sema6A receptor PlxnA4, which is expressed by CST axons. Guidance at the MHB, however, appears independent of this and of the other known receptor, PlxnA2, and may depend instead on Sema6A expression on CST axons themselves at embryonic stages. CONCLUSION: These data identify Sema6A as a major contributor to the guidance of CST axons at multiple choice points. They highlight the active control of guidance at the MHB and also implicate the inferior olive as an important structure in the guidance of CST axons within the hindbrain. They also suggest that Sema6A, which is strongly expressed by oligodendrocytes, may affect CST regeneration in adults. BioMed Central 2008-12-08 /pmc/articles/PMC2647909/ /pubmed/19063725 http://dx.doi.org/10.1186/1749-8104-3-34 Text en Copyright © 2008 Rünker et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Rünker, Annette E
Little, Graham E
Suto, Fumikazu
Fujisawa, Hajime
Mitchell, Kevin J
Semaphorin-6A controls guidance of corticospinal tract axons at multiple choice points
title Semaphorin-6A controls guidance of corticospinal tract axons at multiple choice points
title_full Semaphorin-6A controls guidance of corticospinal tract axons at multiple choice points
title_fullStr Semaphorin-6A controls guidance of corticospinal tract axons at multiple choice points
title_full_unstemmed Semaphorin-6A controls guidance of corticospinal tract axons at multiple choice points
title_short Semaphorin-6A controls guidance of corticospinal tract axons at multiple choice points
title_sort semaphorin-6a controls guidance of corticospinal tract axons at multiple choice points
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2647909/
https://www.ncbi.nlm.nih.gov/pubmed/19063725
http://dx.doi.org/10.1186/1749-8104-3-34
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