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Semaphorin 6B acts as a receptor in post-crossing commissural axon guidance

Andermatt, Irwin; Wilson, Nicole H; Bergmann, Timothy; Mauti, Olivier; Gesemann, Matthias; Sockanathan, Shanthini; Stoeckli, Esther T (2014). Semaphorin 6B acts as a receptor in post-crossing commissural axon guidance. Development, 141(19):3709-3720.

Abstract

Semaphorins are a large family of axon guidance molecules that are known primarily as ligands for plexins and neuropilins. Although class-6 semaphorins are transmembrane proteins, they have been implicated as ligands in different aspects of neural development, including neural crest cell migration, axon guidance and cerebellar development. However, the specific spatial and temporal expression of semaphorin 6B (Sema6B) in chick commissural neurons suggested a receptor role in axon guidance at the spinal cord midline. Indeed, in the absence of Sema6B, post-crossing commissural axons lacked an instructive signal directing them rostrally along the contralateral floorplate border, resulting in stalling at the exit site or even caudal turns. Truncated Sema6B lacking the intracellular domain was unable to rescue the loss-of-function phenotype, confirming a receptor function of Sema6B. In support of this, we demonstrate that Sema6B binds to floorplate-derived plexin A2 (PlxnA2) for navigation at the midline, whereas a cis-interaction between PlxnA2 and Sema6B on pre-crossing commissural axons may regulate the responsiveness of axons to floorplate-derived cues.

Additional indexing

Item Type:Journal Article, refereed, original work
Communities & Collections:07 Faculty of Science > Institute of Molecular Life Sciences
Dewey Decimal Classification:570 Life sciences; biology
Scopus Subject Areas:Life Sciences > Molecular Biology
Life Sciences > Developmental Biology
Uncontrolled Keywords:pinal cord development, In ovo RNAi, Cis-interaction,, , PlexinA2, Chick
Language:English
Date:2014
Deposited On:19 Nov 2014 11:30
Last Modified:12 Sep 2024 01:35
Publisher:Company of Biologists
ISSN:0950-1991
OA Status:Hybrid
Free access at:PubMed ID. An embargo period may apply.
Publisher DOI:https://doi.org/10.1242/dev.112185
PubMed ID:25209245
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