In Vitro Model of Human Skeletal Muscle Tissues with Contractility Fabricated by Immortalized Human Myogenic Cells.
Takunori NagashimaStacy HadiwidjajaSaki OhsumiAkari MurataTakumi HisadaRyuji KatoYohei OkadaHiroyuki HondaKazunori ShimizuPublished in: Advanced biosystems (2020)
In the development process for drugs used to treat skeletal muscle, cell-based contractile force assays have been considered as a useful in vitro test. Immortalized human myogenic cells are promising as cell sources for reproducible and well-characterized in vitro models. In this study, it is investigated whether immortalized human myogenic cells, Hu5/KD3, have suitable contractile ability and the potential to be used as cell sources for contractile force assays. Muscle tissues are fabricated using Hu5/KD3 cells on the microfabricated devices used to measure contractile force. The tissues generate a tetanic force of ≈30 µN in response to the electrical pulse stimulation (EPS). Gene expression analysis of the myosin heavy chain (MYH) isoform indicates that the tissues mostly consisted of muscle fibers expressing MYH7 or/and MYH8. The addition of dexamethasone or lovastatin decreases the contractile force of the tissues, indicating that the tissues have the potential to evaluate drug candidates designed to treat muscle atrophy or statin-induced myopathy. It is also demonstrated that the contractile force of tissues increased when EPS is applied as an artificial exercise. These results indicate that the Hu5/KD3 tissues can be employed for contractile force assays and would be useful for in vitro human skeletal muscle models.
Keyphrases
- skeletal muscle
- gene expression
- endothelial cells
- insulin resistance
- induced apoptosis
- single molecule
- cell cycle arrest
- induced pluripotent stem cells
- pluripotent stem cells
- cardiovascular disease
- single cell
- high throughput
- metabolic syndrome
- stem cells
- high glucose
- dna methylation
- cell death
- oxidative stress
- heart failure
- bone marrow
- blood pressure
- emergency department
- mass spectrometry
- high dose
- signaling pathway
- cell proliferation
- coronary artery disease
- adipose tissue
- left ventricular
- risk assessment
- late onset
- adverse drug
- stress induced
- diabetic rats
- human health