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SlitC-PlexinA1 mediates iterative inhibition for orderly passage of spinal commissural axons through the floor plate

Spinal commissural axon navigation across the midline in the floor plate requires repulsive forces from local Slit repellents. The long-held view is that Slits push growth cones forward and prevent them from turning back once they became sensitized to these cues after midline crossing. We analyzed w...

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Autores principales: Ducuing, Hugo, Gardette, Thibault, Pignata, Aurora, Kindbeiter, Karine, Bozon, Muriel, Thoumine, Olivier, Delloye-Bourgeois, Céline, Tauszig-Delamasure, Servane, Castellani, Valerie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7775108/
https://www.ncbi.nlm.nih.gov/pubmed/33345773
http://dx.doi.org/10.7554/eLife.63205
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author Ducuing, Hugo
Gardette, Thibault
Pignata, Aurora
Kindbeiter, Karine
Bozon, Muriel
Thoumine, Olivier
Delloye-Bourgeois, Céline
Tauszig-Delamasure, Servane
Castellani, Valerie
author_facet Ducuing, Hugo
Gardette, Thibault
Pignata, Aurora
Kindbeiter, Karine
Bozon, Muriel
Thoumine, Olivier
Delloye-Bourgeois, Céline
Tauszig-Delamasure, Servane
Castellani, Valerie
author_sort Ducuing, Hugo
collection PubMed
description Spinal commissural axon navigation across the midline in the floor plate requires repulsive forces from local Slit repellents. The long-held view is that Slits push growth cones forward and prevent them from turning back once they became sensitized to these cues after midline crossing. We analyzed with fluorescent reporters Slits distribution and FP glia morphology. We observed clusters of Slit-N and Slit-C fragments decorating a complex architecture of glial basal process ramifications. We found that PC2 proprotein convertase activity contributes to this pattern of ligands. Next, we studied Slit-C acting via PlexinA1 receptor shared with another FP repellent, the Semaphorin3B, through generation of a mouse model baring PlexinA1(Y1815F) mutation abrogating SlitC but not Sema3B responsiveness, manipulations in the chicken embryo, and ex vivo live imaging. This revealed a guidance mechanism by which SlitC constantly limits growth cone exploration, imposing ordered and forward-directed progression through aligned corridors formed by FP basal ramifications.
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spelling pubmed-77751082021-01-04 SlitC-PlexinA1 mediates iterative inhibition for orderly passage of spinal commissural axons through the floor plate Ducuing, Hugo Gardette, Thibault Pignata, Aurora Kindbeiter, Karine Bozon, Muriel Thoumine, Olivier Delloye-Bourgeois, Céline Tauszig-Delamasure, Servane Castellani, Valerie eLife Developmental Biology Spinal commissural axon navigation across the midline in the floor plate requires repulsive forces from local Slit repellents. The long-held view is that Slits push growth cones forward and prevent them from turning back once they became sensitized to these cues after midline crossing. We analyzed with fluorescent reporters Slits distribution and FP glia morphology. We observed clusters of Slit-N and Slit-C fragments decorating a complex architecture of glial basal process ramifications. We found that PC2 proprotein convertase activity contributes to this pattern of ligands. Next, we studied Slit-C acting via PlexinA1 receptor shared with another FP repellent, the Semaphorin3B, through generation of a mouse model baring PlexinA1(Y1815F) mutation abrogating SlitC but not Sema3B responsiveness, manipulations in the chicken embryo, and ex vivo live imaging. This revealed a guidance mechanism by which SlitC constantly limits growth cone exploration, imposing ordered and forward-directed progression through aligned corridors formed by FP basal ramifications. eLife Sciences Publications, Ltd 2020-12-21 /pmc/articles/PMC7775108/ /pubmed/33345773 http://dx.doi.org/10.7554/eLife.63205 Text en © 2020, Ducuing et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Developmental Biology
Ducuing, Hugo
Gardette, Thibault
Pignata, Aurora
Kindbeiter, Karine
Bozon, Muriel
Thoumine, Olivier
Delloye-Bourgeois, Céline
Tauszig-Delamasure, Servane
Castellani, Valerie
SlitC-PlexinA1 mediates iterative inhibition for orderly passage of spinal commissural axons through the floor plate
title SlitC-PlexinA1 mediates iterative inhibition for orderly passage of spinal commissural axons through the floor plate
title_full SlitC-PlexinA1 mediates iterative inhibition for orderly passage of spinal commissural axons through the floor plate
title_fullStr SlitC-PlexinA1 mediates iterative inhibition for orderly passage of spinal commissural axons through the floor plate
title_full_unstemmed SlitC-PlexinA1 mediates iterative inhibition for orderly passage of spinal commissural axons through the floor plate
title_short SlitC-PlexinA1 mediates iterative inhibition for orderly passage of spinal commissural axons through the floor plate
title_sort slitc-plexina1 mediates iterative inhibition for orderly passage of spinal commissural axons through the floor plate
topic Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7775108/
https://www.ncbi.nlm.nih.gov/pubmed/33345773
http://dx.doi.org/10.7554/eLife.63205
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