Three-Dimensional Human iPSC-Derived Artificial Skeletal Muscles Model Muscular Dystrophies and Enable Multilineage Tissue Engineering
Author(s) -
Sara M. Maffioletti,
Shilpita Sarcar,
A. Henderson,
Ingra Mannhardt,
Luca Pinton,
Louise A. Moyle,
Heather Steele-Stallard,
Ornella Cappellari,
Kim E. Wells,
Giuliana Ferrari,
Jamie S. Mitchell,
Giulia E. Tyzack,
Vassilios N. Kotiadis,
Moustafa Khedr,
Martina Ragazzi,
Weixin Wang,
Michael R. Duchen,
Rickie Patani,
Peter S. Zammit,
Dominic J. Wells,
Thomas Eschenhagen,
Francesco Saverio Tedesco
Publication year - 2018
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2018.03.091
Subject(s) - induced pluripotent stem cell , skeletal muscle , myocyte , regenerative medicine , muscular dystrophy , biology , duchenne muscular dystrophy , myogenesis , microbiology and biotechnology , stem cell , anatomy , embryonic stem cell , genetics , gene
Generating human skeletal muscle models is instrumental for investigating muscle pathology and therapy. Here, we report the generation of three-dimensional (3D) artificial skeletal muscle tissue from human pluripotent stem cells, including induced pluripotent stem cells (iPSCs) from patients with Duchenne, limb-girdle, and congenital muscular dystrophies. 3D skeletal myogenic differentiation of pluripotent cells was induced within hydrogels under tension to provide myofiber alignment. Artificial muscles recapitulated characteristics of human skeletal muscle tissue and could be implanted into immunodeficient mice. Pathological cellular hallmarks of incurable forms of severe muscular dystrophy could be modeled with high fidelity using this 3D platform. Finally, we show generation of fully human iPSC-derived, complex, multilineage muscle models containing key isogenic cellular constituents of skeletal muscle, including vascular endothelial cells, pericytes, and motor neurons. These results lay the foundation for a human skeletal muscle organoid-like platform for disease modeling, regenerative medicine, and therapy development.
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