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.

Urciuolo, A., Serena, E., Ghua, R., Zatti, S., Giomo, M., Mattei, N., et al. (2020). Engineering a 3D in vitro model of human skeletal muscle at the single fiber scale. PLOS ONE, 15(5), 1-17 [10.1371/journal.pone.0232081].

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

Luni, Camilla;
2020

Abstract

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.
2020
Urciuolo, A., Serena, E., Ghua, R., Zatti, S., Giomo, M., Mattei, N., et al. (2020). Engineering a 3D in vitro model of human skeletal muscle at the single fiber scale. PLOS ONE, 15(5), 1-17 [10.1371/journal.pone.0232081].
Urciuolo, Anna; Serena, Elena; Ghua, Rusha; Zatti, Susi; Giomo, Monica; Mattei, Nicolò; Vetralla, Massimo; Selmin, Giulia; Luni, Camilla; Vitulo, Nico...espandi
File in questo prodotto:
File Dimensione Formato  
journal.pone.0232081.pdf

accesso aperto

Tipo: Versione (PDF) editoriale
Licenza: Creative commons
Dimensione 2.57 MB
Formato Adobe PDF
2.57 MB Adobe PDF Visualizza/Apri
02_27Urciuolo_muscolo3D 2020_FigS1.pdf

accesso aperto

Tipo: File Supplementare
Licenza: Creative commons
Dimensione 70.87 kB
Formato Adobe PDF
70.87 kB Adobe PDF Visualizza/Apri
02_27Urciuolo_muscolo3D 2020_FigS2.pdf

accesso aperto

Tipo: File Supplementare
Licenza: Creative commons
Dimensione 2.76 MB
Formato Adobe PDF
2.76 MB Adobe PDF Visualizza/Apri
02_27Urciuolo_muscolo3D 2020_FigS3.pdf

accesso aperto

Tipo: File Supplementare
Licenza: Creative commons
Dimensione 1.05 MB
Formato Adobe PDF
1.05 MB Adobe PDF Visualizza/Apri
02_27Urciuolo_muscolo3D 2020_FigS4.pdf

accesso aperto

Tipo: Versione (PDF) editoriale
Licenza: Creative commons
Dimensione 98.18 kB
Formato Adobe PDF
98.18 kB Adobe PDF Visualizza/Apri

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/776338
Citazioni
  • ???jsp.display-item.citation.pmc??? 11
  • Scopus 25
  • ???jsp.display-item.citation.isi??? 22
social impact