Abstract

Skeletal muscle possesses remarkable plasticity that permits functional adaptations to a wide range of signals such as motor input, exercise, and disease. Small animal models have been pivotal in elucidating the molecular mechanisms regulating skeletal muscle adaptation and plasticity. However, these small animal models fail to accurately model human muscle disease resulting in poor clinical success of therapies. Here, we review the potential of in vitro three-dimensional tissue-engineered skeletal muscle models to study muscle function, plasticity, and disease. First, we discuss the generation and function of in vitro skeletal muscle models. We then discuss the genetic, neural, and hormonal factors regulating skeletal muscle fiber-type in vivo and the ability of current in vitro models to study muscle fiber-type regulation. We also evaluate the potential of these systems to be utilized in a patient-specific manner to accurately model and gain novel insights into diseases such as Duchenne muscular dystrophy (DMD) and volumetric muscle loss. We conclude with a discussion on future developments required for tissue-engineered skeletal muscle models to become more mature, biomimetic, and widely utilized for studying muscle physiology, disease, and clinical use.

Highlights

  • Skeletal muscle is the largest organ in the body by mass and is essential for respiration, locomotion, posture, and whole-body energy homeostasis

  • The recent advances and progress made in tissue engineering more biomimetic muscle tissues has provided researchers a novel model to complement traditional 2D cell culture and animal models

  • We have discussed the utility of these engineered tissues to study muscle physiology, regeneration, exercise, and disease

Read more

Summary

Introduction

Skeletal muscle is the largest organ in the body by mass and is essential for respiration, locomotion, posture, and whole-body energy homeostasis. Slow contractile and calcium-handling isoforms result in slower contractile kinetics and importantly permit more energy efficient contraction by utilizing less ATP to generate equivalent contractile forces than fast muscle fibers (Bottinelli et al, 1994; Stienen et al, 1996).

Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call