High-throughput, real-time monitoring of engineered skeletal muscle function using magnetic sensing.
Alec Simon Tulloch SmithShawn M LuttrellJean-Baptiste DupontKevin GrayDaniel LihJacob W FlemingNathan J CunninghamSofia JepsonJennifer HessonJulie MathieuLisa MavesBonnie J BerryElliot C FisherNathan J SniadeckiNicholas A GeisseDavid L MackPublished in: Journal of tissue engineering (2022)
Engineered muscle tissues represent powerful tools for examining tissue level contractile properties of skeletal muscle. However, limitations in the throughput associated with standard analysis methods limit their utility for longitudinal study, high throughput drug screens, and disease modeling. Here we present a method for integrating 3D engineered skeletal muscles with a magnetic sensing system to facilitate non-invasive, longitudinal analysis of developing contraction kinetics. Using this platform, we show that engineered skeletal muscle tissues derived from both induced pluripotent stem cell and primary sources undergo improvements in contractile output over time in culture. We demonstrate how magnetic sensing of contractility can be employed for simultaneous assessment of multiple tissues subjected to different doses of known skeletal muscle inotropes as well as the stratification of healthy versus diseased functional profiles in normal and dystrophic muscle cells. Based on these data, this combined culture system and magnet-based contractility platform greatly broadens the potential for 3D engineered skeletal muscle tissues to impact the translation of novel therapies from the lab to the clinic.
Keyphrases
- skeletal muscle
- high throughput
- insulin resistance
- gene expression
- stem cells
- molecularly imprinted
- single cell
- smooth muscle
- induced apoptosis
- primary care
- emergency department
- type diabetes
- dna methylation
- machine learning
- electronic health record
- drug induced
- cell death
- risk assessment
- genome wide
- diabetic rats
- adipose tissue
- mesenchymal stem cells
- high resolution
- bone marrow
- endothelial cells
- endoplasmic reticulum stress
- signaling pathway
- human health
- solid phase extraction
- mass spectrometry
- clinical evaluation
- adverse drug
- data analysis