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

Author:

Ducuing Hugo1ORCID,Gardette Thibault1,Pignata Aurora1,Kindbeiter Karine1,Bozon Muriel1,Thoumine Olivier2ORCID,Delloye-Bourgeois Céline1,Tauszig-Delamasure Servane1ORCID,Castellani Valerie1ORCID

Affiliation:

1. Institut NeuroMyoGène - CNRS UMR 5310 - INSERM U1217 de Lyon- UCBL Lyon 1, Faculté de Médecine et de Pharmacie, Lyon, France

2. Interdisciplinary Institute for Neuroscience, UMR CNRS 5297 - University of Bordeaux, Bordeaux, France

Abstract

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 PlexinA1Y1815F 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.

Funder

Agence Nationale de la Recherche

Fondation pour la Recherche Médicale

Fondation Bettencourt Schueller

AFM-Téléthon

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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