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Semaphorin signaling restricts neuronal regeneration in C. elegans

Extracellular signaling proteins serve as neuronal growth cone guidance molecules during development and are well positioned to be involved in neuronal regeneration and recovery from injury. Semaphorins and their receptors, the plexins, are a family of conserved proteins involved in development that...

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Autores principales: Harreguy, Maria B, Tanvir, Zainab, Shah, Esha, Simprevil, Blandine, Tran, Tracy S, Haspel, Gal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9618706/
https://www.ncbi.nlm.nih.gov/pubmed/36325362
http://dx.doi.org/10.3389/fcell.2022.814160
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author Harreguy, Maria B
Tanvir, Zainab
Shah, Esha
Simprevil, Blandine
Tran, Tracy S
Haspel, Gal
author_facet Harreguy, Maria B
Tanvir, Zainab
Shah, Esha
Simprevil, Blandine
Tran, Tracy S
Haspel, Gal
author_sort Harreguy, Maria B
collection PubMed
description Extracellular signaling proteins serve as neuronal growth cone guidance molecules during development and are well positioned to be involved in neuronal regeneration and recovery from injury. Semaphorins and their receptors, the plexins, are a family of conserved proteins involved in development that, in the nervous system, are axonal guidance cues mediating axon pathfinding and synapse formation. The Caenorhabditis elegans genome encodes for three semaphorins and two plexin receptors: the transmembrane semaphorins, SMP-1 and SMP-2, signal through their receptor, PLX-1, while the secreted semaphorin, MAB-20, signals through PLX-2. Here, we evaluate the locomotion behavior of knockout animals missing each of the semaphorins and plexins and the neuronal morphology of plexin knockout animals; we described the cellular expression pattern of the promoters of all plexins in the nervous system of C. elegans; and we evaluated their effect on the regrowth and reconnection of motoneuron neurites and the recovery of locomotion behavior following precise laser microsurgery. Regrowth and reconnection were more prevalent in the absence of each plexin, while recovery of locomotion surpassed regeneration in all genotypes.
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spelling pubmed-96187062022-11-01 Semaphorin signaling restricts neuronal regeneration in C. elegans Harreguy, Maria B Tanvir, Zainab Shah, Esha Simprevil, Blandine Tran, Tracy S Haspel, Gal Front Cell Dev Biol Cell and Developmental Biology Extracellular signaling proteins serve as neuronal growth cone guidance molecules during development and are well positioned to be involved in neuronal regeneration and recovery from injury. Semaphorins and their receptors, the plexins, are a family of conserved proteins involved in development that, in the nervous system, are axonal guidance cues mediating axon pathfinding and synapse formation. The Caenorhabditis elegans genome encodes for three semaphorins and two plexin receptors: the transmembrane semaphorins, SMP-1 and SMP-2, signal through their receptor, PLX-1, while the secreted semaphorin, MAB-20, signals through PLX-2. Here, we evaluate the locomotion behavior of knockout animals missing each of the semaphorins and plexins and the neuronal morphology of plexin knockout animals; we described the cellular expression pattern of the promoters of all plexins in the nervous system of C. elegans; and we evaluated their effect on the regrowth and reconnection of motoneuron neurites and the recovery of locomotion behavior following precise laser microsurgery. Regrowth and reconnection were more prevalent in the absence of each plexin, while recovery of locomotion surpassed regeneration in all genotypes. Frontiers Media S.A. 2022-10-17 /pmc/articles/PMC9618706/ /pubmed/36325362 http://dx.doi.org/10.3389/fcell.2022.814160 Text en Copyright © 2022 Harreguy, Tanvir, Shah, Simprevil, Tran and Haspel. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Harreguy, Maria B
Tanvir, Zainab
Shah, Esha
Simprevil, Blandine
Tran, Tracy S
Haspel, Gal
Semaphorin signaling restricts neuronal regeneration in C. elegans
title Semaphorin signaling restricts neuronal regeneration in C. elegans
title_full Semaphorin signaling restricts neuronal regeneration in C. elegans
title_fullStr Semaphorin signaling restricts neuronal regeneration in C. elegans
title_full_unstemmed Semaphorin signaling restricts neuronal regeneration in C. elegans
title_short Semaphorin signaling restricts neuronal regeneration in C. elegans
title_sort semaphorin signaling restricts neuronal regeneration in c. elegans
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9618706/
https://www.ncbi.nlm.nih.gov/pubmed/36325362
http://dx.doi.org/10.3389/fcell.2022.814160
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