Optimizing electrical field stimulation parameters reveals the maximum contractile function of human skeletal muscle microtissues.

IF 4.7 2区 生物学 Q2 CELL BIOLOGY American journal of physiology. Cell physiology Pub Date : 2025-04-01 Epub Date: 2025-02-28 DOI:10.1152/ajpcell.00308.2024
Yekaterina Tiper, Zhuoye Xie, Arne Hofemeier, Heta Lad, Mattias Luber, Roman Krawetz, Timo Betz, Wolfram-Hubertus Zimmermann, Aaron B Morton, Steven S Segal, Penney M Gilbert
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Abstract

Skeletal muscle microtissues are engineered to develop therapies for restoring muscle function in patients. However, optimal electrical field stimulation (EFS) parameters to evaluate the function of muscle microtissues remain unestablished. This study reports a protocol to optimize EFS parameters for eliciting contractile force of muscle microtissues cultured in micropost platforms. Muscle microtissues were produced across an opposing pair of microposts in polydimethylsiloxane and polymethyl methacrylate culture platforms using primary, immortalized, and induced pluripotent stem cell-derived myoblasts. In response to EFS between needle electrodes, contraction deflects microposts proportional to developed force. At 5 V, pulse durations used for native muscle (0.1-1 ms) failed to elicit contraction of microtissues; durations reported for engineered muscle (5-10 ms) failed to elicit peak force. Instead, pulse durations of 20-80 ms were required to elicit peak twitch force across microtissues derived from five myoblast lines. Similarly, although peak tetanic force occurs at 20-50 Hz for native human muscles, it varied across microtissues depending on the cell line type, ranging from 7 to 60 Hz. A new parameter, the dynamic oscillation of force, captured trends during rhythmic contractions, whereas quantifying the duration-at-peak force provides an extended kinetics parameter. Our findings indicate that muscle microtissues have cell line type-specific contractile properties, yet all contract and relax more slowly than native muscle, implicating underdeveloped excitation-contraction coupling. Failure to optimize EFS parameters can mask the functional potential of muscle microtissues by underestimating force production. Optimizing and reporting EFS parameters and metrics is necessary to leverage muscle microtissues for advancing skeletal muscle therapies.NEW & NOTEWORTHY Electrical field stimulation (EFS) parameters remain to be standardized for engineered skeletal muscle. Herein, we report a protocol for defining EFS parameters that elicit the maximal contractile force of muscle microtissues cultivated in micropost devices and highlight the value of developing appropriate metrics. The dynamic oscillation of force and duration-at-peak force are introduced as novel metrics of contraction kinetics.

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优化电场刺激参数揭示人体骨骼肌微组织的最大收缩功能。
骨骼肌微组织被设计用于开发恢复患者肌肉功能的疗法。然而,评估肌肉微组织功能的最佳电场刺激(EFS)参数仍未建立。本研究报告了一种方案,以优化在微帖子平台培养的肌肉微组织的激发收缩力的EFS参数。在聚二甲基硅氧烷和聚甲基丙烯酸甲酯培养平台上,使用原代、永生化和诱导的多能干细胞衍生的成肌细胞,在相对的微柱上产生肌肉微组织。在针电极之间的电场作用下,收缩使微柱的偏转与发展的力成正比。在5 V时,原生肌肉的脉冲持续时间(0.1-1 ms)未能引起显微组织的收缩;工程肌肉的持续时间(5-10毫秒)未能引起峰值力。相反,需要20-80毫秒的脉冲持续时间才能引起来自5种成肌细胞系的微组织的峰值抽搐力。同样,虽然天然人体肌肉的破伤风力峰值出现在20-50 Hz,但根据细胞系类型,它在不同的显微组织中各不相同,范围从7-60 Hz。一个新的参数,力的动态振荡,捕捉了节律性收缩的趋势,同时量化了峰值力的持续时间,提供了一个扩展的动力学参数。我们的研究结果表明,肌肉微组织具有细胞系类型特异性的收缩特性,但所有的收缩和放松都比天然肌肉慢,这意味着不发达的兴奋-收缩耦合。失败的优化EFS参数可以掩盖肌肉微组织的功能潜力,低估力生产。优化和报告EFS参数和指标对于利用肌肉微组织推进骨骼肌治疗是必要的。
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来源期刊
CiteScore
9.10
自引率
1.80%
发文量
252
审稿时长
1 months
期刊介绍: The American Journal of Physiology-Cell Physiology is dedicated to innovative approaches to the study of cell and molecular physiology. Contributions that use cellular and molecular approaches to shed light on mechanisms of physiological control at higher levels of organization also appear regularly. Manuscripts dealing with the structure and function of cell membranes, contractile systems, cellular organelles, and membrane channels, transporters, and pumps are encouraged. Studies dealing with integrated regulation of cellular function, including mechanisms of signal transduction, development, gene expression, cell-to-cell interactions, and the cell physiology of pathophysiological states, are also eagerly sought. Interdisciplinary studies that apply the approaches of biochemistry, biophysics, molecular biology, morphology, and immunology to the determination of new principles in cell physiology are especially welcome.
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