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Engineered skeletal muscles for disease modeling and drug discovery
- Source :
- Biomaterials
- Publication Year :
- 2019
- Publisher :
- Elsevier BV, 2019.
-
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.
- Subjects :
- Dysferlinopathy
Duchenne muscular dystrophy
Induced Pluripotent Stem Cells
Biophysics
Bioengineering
02 engineering and technology
Disease
Organ-on-a-chip
Muscular Dystrophies
Article
Biomaterials
03 medical and health sciences
Drug Discovery
Humans
Medicine
Muscle, Skeletal
030304 developmental biology
0303 health sciences
Tissue Engineering
business.industry
Drug discovery
Regeneration (biology)
Skeletal muscle
021001 nanoscience & nanotechnology
medicine.disease
medicine.anatomical_structure
Drug development
Mechanics of Materials
Ceramics and Composites
0210 nano-technology
business
Neuroscience
Subjects
Details
- ISSN :
- 01429612
- Volume :
- 221
- Database :
- OpenAIRE
- Journal :
- Biomaterials
- Accession number :
- edsair.doi.dedup.....c55a5692a6d7fcc46019a5f27e55e840
- Full Text :
- https://doi.org/10.1016/j.biomaterials.2019.119416