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Botulinum Toxin Treatment of Adult Muscle Stem Cells from Children with Cerebral Palsy and hiPSC-Derived Neuromuscular Junctions

Botulinum neurotoxin type-A (BoNT) injections are commonly used as spasticity treatment in cerebral palsy (CP). Despite improved clinical outcomes, concerns regarding harmful effects on muscle morphology have been raised, and the BoNT effect on muscle stem cells remains not well defined. This study...

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Autores principales: Costamagna, Domiziana, Bastianini, Valeria, Corvelyn, Marlies, Duelen, Robin, Deschrevel, Jorieke, De Beukelaer, Nathalie, De Houwer, Hannah, Sampaolesi, Maurilio, Gayan-Ramirez, Ghislaine, Campenhout, Anja Van, Desloovere, Kaat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10453788/
https://www.ncbi.nlm.nih.gov/pubmed/37626881
http://dx.doi.org/10.3390/cells12162072
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author Costamagna, Domiziana
Bastianini, Valeria
Corvelyn, Marlies
Duelen, Robin
Deschrevel, Jorieke
De Beukelaer, Nathalie
De Houwer, Hannah
Sampaolesi, Maurilio
Gayan-Ramirez, Ghislaine
Campenhout, Anja Van
Desloovere, Kaat
author_facet Costamagna, Domiziana
Bastianini, Valeria
Corvelyn, Marlies
Duelen, Robin
Deschrevel, Jorieke
De Beukelaer, Nathalie
De Houwer, Hannah
Sampaolesi, Maurilio
Gayan-Ramirez, Ghislaine
Campenhout, Anja Van
Desloovere, Kaat
author_sort Costamagna, Domiziana
collection PubMed
description Botulinum neurotoxin type-A (BoNT) injections are commonly used as spasticity treatment in cerebral palsy (CP). Despite improved clinical outcomes, concerns regarding harmful effects on muscle morphology have been raised, and the BoNT effect on muscle stem cells remains not well defined. This study aims at clarifying the impact of BoNT on growing muscles (1) by analyzing the in vitro effect of BoNT on satellite cell (SC)-derived myoblasts and fibroblasts obtained from medial gastrocnemius microbiopsies collected in young BoNT-naïve children (t0) compared to age ranged typically developing children; (2) by following the effect of in vivo BoNT administration on these cells obtained from the same children with CP at 3 (t1) and 6 (t2) months post BoNT; (3) by determining the direct effect of a single and repeated in vitro BoNT treatment on neuromuscular junctions (NMJs) differentiated from hiPSCs. In vitro BoNT did not affect myogenic differentiation or collagen production. The fusion index significantly decreased in CP at t2 compared to t0. In NMJ cocultures, BoNT treatment caused axonal swelling and fragmentation. Repeated treatments impaired the autophagic–lysosomal system. Further studies are warranted to understand the long-term and collateral effects of BoNT in the muscles of children with CP.
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spelling pubmed-104537882023-08-26 Botulinum Toxin Treatment of Adult Muscle Stem Cells from Children with Cerebral Palsy and hiPSC-Derived Neuromuscular Junctions Costamagna, Domiziana Bastianini, Valeria Corvelyn, Marlies Duelen, Robin Deschrevel, Jorieke De Beukelaer, Nathalie De Houwer, Hannah Sampaolesi, Maurilio Gayan-Ramirez, Ghislaine Campenhout, Anja Van Desloovere, Kaat Cells Article Botulinum neurotoxin type-A (BoNT) injections are commonly used as spasticity treatment in cerebral palsy (CP). Despite improved clinical outcomes, concerns regarding harmful effects on muscle morphology have been raised, and the BoNT effect on muscle stem cells remains not well defined. This study aims at clarifying the impact of BoNT on growing muscles (1) by analyzing the in vitro effect of BoNT on satellite cell (SC)-derived myoblasts and fibroblasts obtained from medial gastrocnemius microbiopsies collected in young BoNT-naïve children (t0) compared to age ranged typically developing children; (2) by following the effect of in vivo BoNT administration on these cells obtained from the same children with CP at 3 (t1) and 6 (t2) months post BoNT; (3) by determining the direct effect of a single and repeated in vitro BoNT treatment on neuromuscular junctions (NMJs) differentiated from hiPSCs. In vitro BoNT did not affect myogenic differentiation or collagen production. The fusion index significantly decreased in CP at t2 compared to t0. In NMJ cocultures, BoNT treatment caused axonal swelling and fragmentation. Repeated treatments impaired the autophagic–lysosomal system. Further studies are warranted to understand the long-term and collateral effects of BoNT in the muscles of children with CP. MDPI 2023-08-15 /pmc/articles/PMC10453788/ /pubmed/37626881 http://dx.doi.org/10.3390/cells12162072 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Costamagna, Domiziana
Bastianini, Valeria
Corvelyn, Marlies
Duelen, Robin
Deschrevel, Jorieke
De Beukelaer, Nathalie
De Houwer, Hannah
Sampaolesi, Maurilio
Gayan-Ramirez, Ghislaine
Campenhout, Anja Van
Desloovere, Kaat
Botulinum Toxin Treatment of Adult Muscle Stem Cells from Children with Cerebral Palsy and hiPSC-Derived Neuromuscular Junctions
title Botulinum Toxin Treatment of Adult Muscle Stem Cells from Children with Cerebral Palsy and hiPSC-Derived Neuromuscular Junctions
title_full Botulinum Toxin Treatment of Adult Muscle Stem Cells from Children with Cerebral Palsy and hiPSC-Derived Neuromuscular Junctions
title_fullStr Botulinum Toxin Treatment of Adult Muscle Stem Cells from Children with Cerebral Palsy and hiPSC-Derived Neuromuscular Junctions
title_full_unstemmed Botulinum Toxin Treatment of Adult Muscle Stem Cells from Children with Cerebral Palsy and hiPSC-Derived Neuromuscular Junctions
title_short Botulinum Toxin Treatment of Adult Muscle Stem Cells from Children with Cerebral Palsy and hiPSC-Derived Neuromuscular Junctions
title_sort botulinum toxin treatment of adult muscle stem cells from children with cerebral palsy and hipsc-derived neuromuscular junctions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10453788/
https://www.ncbi.nlm.nih.gov/pubmed/37626881
http://dx.doi.org/10.3390/cells12162072
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