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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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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. |
format | Online Article Text |
id | pubmed-9618706 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
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
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title_full | Semaphorin signaling restricts neuronal regeneration in C. elegans
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title_fullStr | Semaphorin signaling restricts neuronal regeneration in C. elegans
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title_full_unstemmed | Semaphorin signaling restricts neuronal regeneration in C. elegans
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title_short | Semaphorin signaling restricts neuronal regeneration in C. elegans
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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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