Development of an in vitro platform for the analysis of contractile and calcium dynamics in single human myotubes†

IF 6.1 2区 工程技术 Q1 BIOCHEMICAL RESEARCH METHODS Lab on a Chip Pub Date : 2024-09-04 DOI:10.1039/D3LC00442B
Camila Vesga-Castro, Laura Mosqueira-Martín, Paul Ubiria-Urkola, Pablo Marco-Moreno, Klaudia González-Imaz, Jorge Rendon-Hinestroza, Ainara Vallejo-Illarramendi and Jacobo Paredes
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Abstract

In vitro myotube cultures are widely used as models for studying muscle pathophysiology, but their limited maturation and heterogeneity pose significant challenges for functional analyses. While they remain the gold standard for studying muscle function in vitro, myotube cultures do not fully recapitulate the complexity and native features of muscle fibers, which may compromise their ability to predict in vivo outcomes. To promote maturation and decrease heterogeneity, we have incorporated engineered structures into myotube cultures, based on a PDMS thin layer with micrometer-sized grooves (μGrooves) placed over a glass substrate. Different sizes and shapes of μGrooves were tested for their ability to promote alignment and fusion of myoblasts and enhance their differentiation into myotubes. A 24 hour electrical field stimulation protocol (4 V, 6 ms, 0.1 Hz) was used to further promote myotube maturation, after which several myotube features were assessed, including myotube alignment, width, fusion index, contractile function, and calcium handling. Our results indicate superior calcium and contractile performance in μGrooved myotubes, particularly with the 100 μm-width 700 μm-long geometry (7 : 1). This platform generated homogeneous and isolated myotubes that reproduced native muscle features, such as excitation–contraction coupling and force-frequency responses. Overall, our 2D muscle platform enables robust high-content assays of calcium dynamics and contractile readouts with increased sensitivity and reproducibility compared to traditional myotube cultures, making it particularly suitable for screening therapeutic candidates for different muscle pathologies.

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开发用于分析单个人类肌管收缩和钙动力学的体外平台
体外肌管培养物被广泛用作研究肌肉病理生理学的模型,但其有限的成熟度和异质性给功能分析带来了巨大挑战。虽然它们仍然是体外研究肌肉功能的黄金标准,但肌管培养物并不能完全再现肌肉纤维的复杂性和原生特征,这可能会影响它们预测体内结果的能力。为了促进成熟和减少异质性,我们在肌管培养物中加入了工程结构,该结构基于玻璃基底上带有微米级凹槽(μGrooves)的 PDMS 薄层。我们测试了不同大小和形状的微凹槽促进成肌细胞排列和融合以及促进它们分化成肌管的能力。我们采用了 24 小时电场刺激方案(4V、6 ms、0.1 Hz)来进一步促进肌管成熟,之后对肌管排列、肌管宽度、融合指数、收缩功能和钙处理进行了评估。我们的结果表明,µGrooved 肌管具有卓越的钙化和收缩性能,尤其是 100 微米宽 700 微米长的几何形状(7:1)。该平台生成的均匀分离的肌管再现了原生肌肉的特征,如兴奋-收缩耦合和力-频率响应。总之,与传统的肌管培养相比,我们的二维肌肉平台能对钙动力学和收缩读数进行稳健的高含量测定,并提高灵敏度和可重复性,因此特别适合筛选不同肌肉病症的候选疗法。
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来源期刊
Lab on a Chip
Lab on a Chip 工程技术-化学综合
CiteScore
11.10
自引率
8.20%
发文量
434
审稿时长
2.6 months
期刊介绍: Lab on a Chip is the premiere journal that publishes cutting-edge research in the field of miniaturization. By their very nature, microfluidic/nanofluidic/miniaturized systems are at the intersection of disciplines, spanning fundamental research to high-end application, which is reflected by the broad readership of the journal. Lab on a Chip publishes two types of papers on original research: full-length research papers and communications. Papers should demonstrate innovations, which can come from technical advancements or applications addressing pressing needs in globally important areas. The journal also publishes Comments, Reviews, and Perspectives.
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