| Literature DB >> 31419653 |
Jason Wang1, Alastair Khodabukus1, Lingjun Rao1, Keith Vandusen1, Nadia Abutaleb1, Nenad Bursac2.
Abstract
Skeletal muscle is the largest organ of human body with several important roles in everyday movement and metabolic homeostasis. The limited ability of small animal models of muscle disease to accurately predict drug efficacy and toxicity in humans has prompted the development in vitro models of human skeletal muscle that fatefully recapitulate cell and tissue level functions and drug responses. We first review methods for development of three-dimensional engineered muscle tissues and organ-on-a-chip microphysiological systems and discuss their potential utility in drug discovery research and development of new regenerative therapies. Furthermore, we describe strategies to increase the functional maturation of engineered muscle, and motivate the importance of incorporating multiple tissue types on the same chip to model organ cross-talk and generate more predictive drug development platforms. Finally, we review the ability of available in vitro systems to model diseases such as type II diabetes, Duchenne muscular dystrophy, Pompe disease, and dysferlinopathy.Entities:
Keywords: Human muscle; Induced pluripotent stem cells; Muscular dystrophy and disease modeling; Organ-on-a-chip; Regeneration; Tissue engineering
Mesh:
Year: 2019 PMID: 31419653 PMCID: PMC7041662 DOI: 10.1016/j.biomaterials.2019.119416
Source DB: PubMed Journal: Biomaterials ISSN: 0142-9612 Impact factor: 12.479