期刊
BIOMATERIALS
卷 293, 期 -, 页码 -出版社
ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2022.121935
关键词
Skeletal muscle microtissues; Microfabrication; Bioengineering; Tissue on-chip; Muscular dystrophy; Disease modeling
We have developed a miniaturized 3D myotube culture chip that can monitor contraction at the single cell level. This technology requires significantly fewer starting materials than current systems and is crucial for evaluating the outcomes of therapeutic procedures for neuromuscular disorders.
Quantification of skeletal muscle functional contraction is essential to assess the outcomes of therapeutic pro-cedures for neuromuscular disorders. Muscle three-dimensional Organ-on-chip models usually require a sub-stantial amount of biological material, which rarely can be obtained from patient biopsies. Here, we developed a miniaturized 3D myotube culture chip with contraction monitoring capacity at the single cell level. Optimized micropatterned substrate design enabled to obtain high culture yields in tightly controlled microenvironments, with myotubes derived from primary human myoblasts displaying spontaneous contractions. Analysis of nuclear morphology confirmed similar myonuclei structure between obtained myotubes and in vivo myofibers, as compared to 2D monolayers. LMNA-related Congenital Muscular Dystrophy (L-CMD) was modeled with suc-cessful development of diseased 3D myotubes displaying reduced contraction. The miniaturized myotube tech-nology can thus be used to study contraction characteristics and evaluate how diseases affect muscle organization and force generation. Importantly, it requires significantly fewer starting materials than current systems, which should substantially improve drug screening capability.
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