Three-Dimensional Human iPSC-Derived Artificial Skeletal Muscles Model Muscular Dystrophies and Enable Multilineage Tissue Engineering

Sara M. Maffioletti(University College London), Shilpita Sarcar(University College London), A. Henderson(University College London), Ingra Mannhardt(Universität Hamburg), Luca Pinton(King's College London), Louise A. Moyle(University College London), Heather B. Steele-Stallard(King's College London), Ornella Cappellari(Royal Veterinary College), Kim E. Wells(Royal Veterinary College), Giuliana Ferrari(University College London), Jamie S. Mitchell(The Francis Crick Institute), Giulia E. Tyzack(The Francis Crick Institute), Vassilios N. Kotiadis(University College London), Moustafa Khedr(University College London), Martina Ragazzi(University College London), Weixin Wang(University College London), Michael R. Duchen(University College London), Rickie Patani(The Francis Crick Institute), Peter S. Zammit(King's College London), Dominic J. Wells(Royal Veterinary College), Thomas Eschenhagen(Universität Hamburg), Francesco Saverio Tedesco(MRC Laboratory for Molecular Cell Biology)
Cell Reports
April 1, 2018
Cited by 322Open Access
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Abstract

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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