Decellularised skeletal muscles allow functional muscle regeneration by promoting host cell migration

Abstract Pathological conditions affecting skeletal muscle function may lead to irreversible volumetric muscle loss (VML). Therapeutic approaches involving acellular matrices represent an emerging and promising strategy to promote regeneration of skeletal muscle following injury. Here we investigate...

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Autores principales: Anna Urciuolo, Luca Urbani, Silvia Perin, Panagiotis Maghsoudlou, Federico Scottoni, Asllan Gjinovci, Henry Collins-Hooper, Stavros Loukogeorgakis, Athanasios Tyraskis, Silvia Torelli, Elena Germinario, Mario Enrique Alvarez Fallas, Carla Julia-Vilella, Simon Eaton, Bert Blaauw, Ketan Patel, Paolo De Coppi
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Publicado: Nature Portfolio 2018
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spelling oai:doaj.org-article:60c000f05b17423389276b399e8a20682021-12-02T15:08:29ZDecellularised skeletal muscles allow functional muscle regeneration by promoting host cell migration10.1038/s41598-018-26371-y2045-2322https://doaj.org/article/60c000f05b17423389276b399e8a20682018-05-01T00:00:00Zhttps://doi.org/10.1038/s41598-018-26371-yhttps://doaj.org/toc/2045-2322Abstract Pathological conditions affecting skeletal muscle function may lead to irreversible volumetric muscle loss (VML). Therapeutic approaches involving acellular matrices represent an emerging and promising strategy to promote regeneration of skeletal muscle following injury. Here we investigated the ability of three different decellularised skeletal muscle scaffolds to support muscle regeneration in a xenogeneic immune-competent model of VML, in which the EDL muscle was surgically resected. All implanted acellular matrices, used to replace the resected muscles, were able to generate functional artificial muscles by promoting host myogenic cell migration and differentiation, as well as nervous fibres, vascular networks, and satellite cell (SC) homing. However, acellular tissue mainly composed of extracellular matrix (ECM) allowed better myofibre three-dimensional (3D) organization and the restoration of SC pool, when compared to scaffolds which also preserved muscular cytoskeletal structures. Finally, we showed that fibroblasts are indispensable to promote efficient migration and myogenesis by muscle stem cells across the scaffolds in vitro. This data strongly support the use of xenogeneic acellular muscles as device to treat VML conditions in absence of donor cell implementation, as well as in vitro model for studying cell interplay during myogenesis.Anna UrciuoloLuca UrbaniSilvia PerinPanagiotis MaghsoudlouFederico ScottoniAsllan GjinovciHenry Collins-HooperStavros LoukogeorgakisAthanasios TyraskisSilvia TorelliElena GerminarioMario Enrique Alvarez FallasCarla Julia-VilellaSimon EatonBert BlaauwKetan PatelPaolo De CoppiNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 8, Iss 1, Pp 1-20 (2018)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Anna Urciuolo
Luca Urbani
Silvia Perin
Panagiotis Maghsoudlou
Federico Scottoni
Asllan Gjinovci
Henry Collins-Hooper
Stavros Loukogeorgakis
Athanasios Tyraskis
Silvia Torelli
Elena Germinario
Mario Enrique Alvarez Fallas
Carla Julia-Vilella
Simon Eaton
Bert Blaauw
Ketan Patel
Paolo De Coppi
Decellularised skeletal muscles allow functional muscle regeneration by promoting host cell migration
description Abstract Pathological conditions affecting skeletal muscle function may lead to irreversible volumetric muscle loss (VML). Therapeutic approaches involving acellular matrices represent an emerging and promising strategy to promote regeneration of skeletal muscle following injury. Here we investigated the ability of three different decellularised skeletal muscle scaffolds to support muscle regeneration in a xenogeneic immune-competent model of VML, in which the EDL muscle was surgically resected. All implanted acellular matrices, used to replace the resected muscles, were able to generate functional artificial muscles by promoting host myogenic cell migration and differentiation, as well as nervous fibres, vascular networks, and satellite cell (SC) homing. However, acellular tissue mainly composed of extracellular matrix (ECM) allowed better myofibre three-dimensional (3D) organization and the restoration of SC pool, when compared to scaffolds which also preserved muscular cytoskeletal structures. Finally, we showed that fibroblasts are indispensable to promote efficient migration and myogenesis by muscle stem cells across the scaffolds in vitro. This data strongly support the use of xenogeneic acellular muscles as device to treat VML conditions in absence of donor cell implementation, as well as in vitro model for studying cell interplay during myogenesis.
format article
author Anna Urciuolo
Luca Urbani
Silvia Perin
Panagiotis Maghsoudlou
Federico Scottoni
Asllan Gjinovci
Henry Collins-Hooper
Stavros Loukogeorgakis
Athanasios Tyraskis
Silvia Torelli
Elena Germinario
Mario Enrique Alvarez Fallas
Carla Julia-Vilella
Simon Eaton
Bert Blaauw
Ketan Patel
Paolo De Coppi
author_facet Anna Urciuolo
Luca Urbani
Silvia Perin
Panagiotis Maghsoudlou
Federico Scottoni
Asllan Gjinovci
Henry Collins-Hooper
Stavros Loukogeorgakis
Athanasios Tyraskis
Silvia Torelli
Elena Germinario
Mario Enrique Alvarez Fallas
Carla Julia-Vilella
Simon Eaton
Bert Blaauw
Ketan Patel
Paolo De Coppi
author_sort Anna Urciuolo
title Decellularised skeletal muscles allow functional muscle regeneration by promoting host cell migration
title_short Decellularised skeletal muscles allow functional muscle regeneration by promoting host cell migration
title_full Decellularised skeletal muscles allow functional muscle regeneration by promoting host cell migration
title_fullStr Decellularised skeletal muscles allow functional muscle regeneration by promoting host cell migration
title_full_unstemmed Decellularised skeletal muscles allow functional muscle regeneration by promoting host cell migration
title_sort decellularised skeletal muscles allow functional muscle regeneration by promoting host cell migration
publisher Nature Portfolio
publishDate 2018
url https://doaj.org/article/60c000f05b17423389276b399e8a2068
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