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Neural cell integration into 3D bioprinted skeletal muscle constructs accelerates restoration of muscle function

Medicine and Health

Neural cell integration into 3D bioprinted skeletal muscle constructs accelerates restoration of muscle function

J. H. Kim, I. Kim, et al.

Discover how the integration of neural cells into bioprinted skeletal muscle constructs, researched by Ji Hyun Kim and colleagues, can significantly enhance muscle regeneration. This innovative approach not only promotes myofiber formation and NMJ development but also restores muscle weight and function in vivo, paving the way for advanced therapies for muscle injuries.

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~3 min • Beginner • English
Abstract
A bioengineered skeletal muscle construct that mimics structural and functional characteristics of native skeletal muscle is a promising therapeutic option to treat extensive muscle defect injuries. We previously showed that bioprinted human skeletal muscle constructs were able to form multi-layered bundles with aligned myofibers. In this study, we investigate the effects of neural cell integration into the bioprinted skeletal muscle construct to accelerate functional muscle regeneration in vivo. Neural input into this bioprinted skeletal muscle construct shows the improvement of myofiber formation, long-term survival, and neuromuscular junction formation in vitro. More importantly, the bioprinted constructs with neural cell integration facilitate rapid innervation and mature into organized muscle tissue that restores normal muscle weight and function in a rodent model of muscle defect injury. These results suggest that the 3D bioprinted human neural-skeletal muscle constructs can be rapidly integrated with the host neural network, resulting in accelerated muscle function restoration.
Publisher
Nature Communications
Published On
Feb 24, 2020
Authors
Ji Hyun Kim, Ickhee Kim, Young-Joon Seol, In Kap Ko, James J. Yoo, Anthony Atala, Sang Jin Lee
Tags
bioengineered skeletal muscle
neural cell integration
3D bioprinted constructs
muscle regeneration
neuromuscular junction
innervation
rodent model
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