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

Author:

Costamagna Domiziana12ORCID,Bastianini Valeria1ORCID,Corvelyn Marlies2,Duelen Robin23ORCID,Deschrevel Jorieke4ORCID,De Beukelaer Nathalie15ORCID,De Houwer Hannah6,Sampaolesi Maurilio2ORCID,Gayan-Ramirez Ghislaine4ORCID,Campenhout Anja Van67ORCID,Desloovere Kaat1

Affiliation:

1. Neurorehabilitation Group, Department of Rehabilitation Sciences, KU Leuven, 3000 Leuven, Belgium

2. Stem Cell and Developmental Biology Unit, Department of Development and Regeneration, KU Leuven, 3000 Leuven, Belgium

3. Cardiology, Department of Cardiovascular Sciences, KU Leuven, 3000 Leuven, Belgium

4. Laboratory of Respiratory Diseases and Thoracic Surgery, Department of Chronic Diseases and Metabolism, KU Leuven, 3000 Leuven, Belgium

5. Willy Taillard Laboratory of Kinesiology, Geneva University Hospitals and University of Geneva, 1211 Geneva, Switzerland

6. Department of Orthopedic Surgery, University Hospitals Leuven, 3000 Leuven, Belgium

7. Department of Development and Regeneration, KU Leuven, 3000 Leuven, Belgium

Abstract

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.

Funder

KU Leuven grant

Scientific Research Flanders

KU Leuven Biomedical Science group: Fund for Translational Biomedical Research 2019

Erasmus Placement 2021 from University of Turin

postdoctoral mandate (PDM) type 1 of KU Leuven

Publisher

MDPI AG

Subject

General Medicine

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