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Engineering a 3D in vitro model of human skeletal muscle at the single fiber scale

The reproduction of reliable in vitro models of human skeletal muscle is made harder by the intrinsic 3D structural complexity of this tissue. Here we coupled engineered hydrogel with 3D structural cues and specific mechanical properties to derive human 3D muscle constructs (“myobundles”) at the sca...

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Autores principales: Urciuolo, Anna, Serena, Elena, Ghua, Rusha, Zatti, Susi, Giomo, Monica, Mattei, Nicolò, Vetralla, Massimo, Selmin, Giulia, Luni, Camilla, Vitulo, Nicola, Valle, Giorgio, Vitiello, Libero, Elvassore, Nicola
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7202609/
https://www.ncbi.nlm.nih.gov/pubmed/32374763
http://dx.doi.org/10.1371/journal.pone.0232081
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author Urciuolo, Anna
Serena, Elena
Ghua, Rusha
Zatti, Susi
Giomo, Monica
Mattei, Nicolò
Vetralla, Massimo
Selmin, Giulia
Luni, Camilla
Vitulo, Nicola
Valle, Giorgio
Vitiello, Libero
Elvassore, Nicola
author_facet Urciuolo, Anna
Serena, Elena
Ghua, Rusha
Zatti, Susi
Giomo, Monica
Mattei, Nicolò
Vetralla, Massimo
Selmin, Giulia
Luni, Camilla
Vitulo, Nicola
Valle, Giorgio
Vitiello, Libero
Elvassore, Nicola
author_sort Urciuolo, Anna
collection PubMed
description The reproduction of reliable in vitro models of human skeletal muscle is made harder by the intrinsic 3D structural complexity of this tissue. Here we coupled engineered hydrogel with 3D structural cues and specific mechanical properties to derive human 3D muscle constructs (“myobundles”) at the scale of single fibers, by using primary myoblasts or myoblasts derived from embryonic stem cells. To this aim, cell culture was performed in confined, laminin-coated micrometric channels obtained inside a 3D hydrogel characterized by the optimal stiffness for skeletal muscle myogenesis. Primary myoblasts cultured in our 3D culture system were able to undergo myotube differentiation and maturation, as demonstrated by the proper expression and localization of key components of the sarcomere and sarcolemma. Such approach allowed the generation of human myobundles of ~10 mm in length and ~120 μm in diameter, showing spontaneous contraction 7 days after cell seeding. Transcriptome analyses showed higher similarity between 3D myobundles and skeletal signature, compared to that found between 2D myotubes and skeletal muscle, mainly resulting from expression in 3D myobundles of categories of genes involved in skeletal muscle maturation, including extracellular matrix organization. Moreover, imaging analyses confirmed that structured 3D culture system was conducive to differentiation/maturation also when using myoblasts derived from embryonic stem cells. In conclusion, our structured 3D model is a promising tool for modelling human skeletal muscle in healthy and diseases conditions.
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spelling pubmed-72026092020-05-12 Engineering a 3D in vitro model of human skeletal muscle at the single fiber scale Urciuolo, Anna Serena, Elena Ghua, Rusha Zatti, Susi Giomo, Monica Mattei, Nicolò Vetralla, Massimo Selmin, Giulia Luni, Camilla Vitulo, Nicola Valle, Giorgio Vitiello, Libero Elvassore, Nicola PLoS One Research Article The reproduction of reliable in vitro models of human skeletal muscle is made harder by the intrinsic 3D structural complexity of this tissue. Here we coupled engineered hydrogel with 3D structural cues and specific mechanical properties to derive human 3D muscle constructs (“myobundles”) at the scale of single fibers, by using primary myoblasts or myoblasts derived from embryonic stem cells. To this aim, cell culture was performed in confined, laminin-coated micrometric channels obtained inside a 3D hydrogel characterized by the optimal stiffness for skeletal muscle myogenesis. Primary myoblasts cultured in our 3D culture system were able to undergo myotube differentiation and maturation, as demonstrated by the proper expression and localization of key components of the sarcomere and sarcolemma. Such approach allowed the generation of human myobundles of ~10 mm in length and ~120 μm in diameter, showing spontaneous contraction 7 days after cell seeding. Transcriptome analyses showed higher similarity between 3D myobundles and skeletal signature, compared to that found between 2D myotubes and skeletal muscle, mainly resulting from expression in 3D myobundles of categories of genes involved in skeletal muscle maturation, including extracellular matrix organization. Moreover, imaging analyses confirmed that structured 3D culture system was conducive to differentiation/maturation also when using myoblasts derived from embryonic stem cells. In conclusion, our structured 3D model is a promising tool for modelling human skeletal muscle in healthy and diseases conditions. Public Library of Science 2020-05-06 /pmc/articles/PMC7202609/ /pubmed/32374763 http://dx.doi.org/10.1371/journal.pone.0232081 Text en © 2020 Urciuolo et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Urciuolo, Anna
Serena, Elena
Ghua, Rusha
Zatti, Susi
Giomo, Monica
Mattei, Nicolò
Vetralla, Massimo
Selmin, Giulia
Luni, Camilla
Vitulo, Nicola
Valle, Giorgio
Vitiello, Libero
Elvassore, Nicola
Engineering a 3D in vitro model of human skeletal muscle at the single fiber scale
title Engineering a 3D in vitro model of human skeletal muscle at the single fiber scale
title_full Engineering a 3D in vitro model of human skeletal muscle at the single fiber scale
title_fullStr Engineering a 3D in vitro model of human skeletal muscle at the single fiber scale
title_full_unstemmed Engineering a 3D in vitro model of human skeletal muscle at the single fiber scale
title_short Engineering a 3D in vitro model of human skeletal muscle at the single fiber scale
title_sort engineering a 3d in vitro model of human skeletal muscle at the single fiber scale
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7202609/
https://www.ncbi.nlm.nih.gov/pubmed/32374763
http://dx.doi.org/10.1371/journal.pone.0232081
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