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Shift in the function of netrin-1 from axon outgrowth to axon branching in developing cerebral cortical neurons

BACKGROUND: Netrin-1, a multifunctional axon guidance cue, elicits axon outgrowth via one of its receptors deleted in colorectal cancer (DCC) in several types of neurons, including cerebral cortical neurons of embryonic mice. However, we and others have observed de novo formation of axon branches wi...

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Autores principales: Matsumoto, Hideko, Nagashima, Masabumi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5645936/
https://www.ncbi.nlm.nih.gov/pubmed/29041904
http://dx.doi.org/10.1186/s12868-017-0392-x
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author Matsumoto, Hideko
Nagashima, Masabumi
author_facet Matsumoto, Hideko
Nagashima, Masabumi
author_sort Matsumoto, Hideko
collection PubMed
description BACKGROUND: Netrin-1, a multifunctional axon guidance cue, elicits axon outgrowth via one of its receptors deleted in colorectal cancer (DCC) in several types of neurons, including cerebral cortical neurons of embryonic mice. However, we and others have observed de novo formation of axon branches without axon outgrowth induced by netrin-1 in cortical culture of neonatal hamsters. These previous reports suggested the possibility that netrin-1 function might alter during development, which we here investigated using dissociated culture prepared from cerebral cortices of embryonic mice. RESULTS: Imaging analysis revealed netrin-1-induced outgrowth in embryonic day (E) 14 axons and netrin-1-induced branching in E16 axons. Netrin-1-evoked filopodial protrusions, which sprouted on the shafts of E16 axons preceding branch formation, were visualized by a novel method called atmospheric scanning electron microscopy. Treatment with an anti-DCC function-blocking antibody affected both axon outgrowth and branching. CONCLUSIONS: Morphological analyses suggested a possibility of a shift in the function of netrin-1 in cortical axons during development, from promotion of outgrowth to promotion of branch formation starting with filopodial protrusion. Function-blocking experiments suggested that DCC may contribute not only to axon outgrowth but branching.
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spelling pubmed-56459362017-10-26 Shift in the function of netrin-1 from axon outgrowth to axon branching in developing cerebral cortical neurons Matsumoto, Hideko Nagashima, Masabumi BMC Neurosci Research Article BACKGROUND: Netrin-1, a multifunctional axon guidance cue, elicits axon outgrowth via one of its receptors deleted in colorectal cancer (DCC) in several types of neurons, including cerebral cortical neurons of embryonic mice. However, we and others have observed de novo formation of axon branches without axon outgrowth induced by netrin-1 in cortical culture of neonatal hamsters. These previous reports suggested the possibility that netrin-1 function might alter during development, which we here investigated using dissociated culture prepared from cerebral cortices of embryonic mice. RESULTS: Imaging analysis revealed netrin-1-induced outgrowth in embryonic day (E) 14 axons and netrin-1-induced branching in E16 axons. Netrin-1-evoked filopodial protrusions, which sprouted on the shafts of E16 axons preceding branch formation, were visualized by a novel method called atmospheric scanning electron microscopy. Treatment with an anti-DCC function-blocking antibody affected both axon outgrowth and branching. CONCLUSIONS: Morphological analyses suggested a possibility of a shift in the function of netrin-1 in cortical axons during development, from promotion of outgrowth to promotion of branch formation starting with filopodial protrusion. Function-blocking experiments suggested that DCC may contribute not only to axon outgrowth but branching. BioMed Central 2017-10-17 /pmc/articles/PMC5645936/ /pubmed/29041904 http://dx.doi.org/10.1186/s12868-017-0392-x Text en © The Author(s) 2017 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
Matsumoto, Hideko
Nagashima, Masabumi
Shift in the function of netrin-1 from axon outgrowth to axon branching in developing cerebral cortical neurons
title Shift in the function of netrin-1 from axon outgrowth to axon branching in developing cerebral cortical neurons
title_full Shift in the function of netrin-1 from axon outgrowth to axon branching in developing cerebral cortical neurons
title_fullStr Shift in the function of netrin-1 from axon outgrowth to axon branching in developing cerebral cortical neurons
title_full_unstemmed Shift in the function of netrin-1 from axon outgrowth to axon branching in developing cerebral cortical neurons
title_short Shift in the function of netrin-1 from axon outgrowth to axon branching in developing cerebral cortical neurons
title_sort shift in the function of netrin-1 from axon outgrowth to axon branching in developing cerebral cortical neurons
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5645936/
https://www.ncbi.nlm.nih.gov/pubmed/29041904
http://dx.doi.org/10.1186/s12868-017-0392-x
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