3D human induced pluripotent stem cell–derived bioengineered skeletal muscles for tissue, disease and therapy modeling

诱导多能干细胞 干细胞 生物 细胞生物学 心肌细胞 祖细胞 组织工程 骨骼肌 细胞疗法 神经科学 电池类型 细胞 解剖 胚胎干细胞 遗传学 基因
作者
Luca Pinton,Moustafa Khedr,Valentina M. Lionello,Shilpita Sarcar,Sara M. Maffioletti,Sumitava Dastidar,Elisa Négroni,SungWoo Choi,Noreen Khokhar,Anne Bigot,John R. Counsell,Andreia S. Bernardo,Peter S. Zammit,Francesco Saverio Tedesco
出处
期刊:Nature Protocols [Nature Portfolio]
卷期号:18 (4): 1337-1376 被引量:45
标识
DOI:10.1038/s41596-022-00790-8
摘要

Skeletal muscle is a complex tissue composed of multinucleated myofibers responsible for force generation that are supported by multiple cell types. Many severe and lethal disorders affect skeletal muscle; therefore, engineering models to reproduce such cellular complexity and function are instrumental for investigating muscle pathophysiology and developing therapies. Here, we detail the modular 3D bioengineering of multilineage skeletal muscles from human induced pluripotent stem cells, which are first differentiated into myogenic, neural and vascular progenitor cells and then combined within 3D hydrogels under tension to generate an aligned myofiber scaffold containing vascular networks and motor neurons. 3D bioengineered muscles recapitulate morphological and functional features of human skeletal muscle, including establishment of a pool of cells expressing muscle stem cell markers. Importantly, bioengineered muscles provide a high-fidelity platform to study muscle pathology, such as emergence of dysmorphic nuclei in muscular dystrophies caused by mutant lamins. The protocol is easy to follow for operators with cell culture experience and takes between 9 and 30 d, depending on the number of cell lineages in the construct. We also provide examples of applications of this advanced platform for testing gene and cell therapies in vitro, as well as for in vivo studies, providing proof of principle of its potential as a tool to develop next-generation neuromuscular or musculoskeletal therapies.
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