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Development of a human skeletal micro muscle platform with pacing capabilities

机译:具有起搏能力的人骨骼微肌平台的开发

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Three dimensional engineered culture systems are powerful tools to rapidly expand our knowledge of human biology and identify novel therapeutic targets for disease. Bioengineered skeletal muscle has been recently shown to recapitulate many features of native muscle biology. However, current skeletal muscle bioengineering approaches require large numbers of cells, reagents and labour, limiting their potential for high-throughput studies. Herein, we use a miniaturized 96-well micro-muscle platform to facilitate semi-automated tissue formation, culture and analysis of human skeletal micro muscles (h mu Ms). Utilising an iterative screening approach we define a serum-free differentiation protocol that drives rapid, directed differentiation of human myoblast to skeletal myofibres. The resulting h mu Ms comprised organised bundles of striated and functional myofibres, which respond appropriately to electrical stimulation. Additionally, we developed an optogenetic approach to chronically stimulate h mu M to recapitulate known features of exercise training including myofibre hypertrophy and increased expression of metabolic proteins. Taken together, our miniaturized approach provides a new platform to enable high-throughput studies of human skeletal muscle biology and exercise physiology.
机译:三维工程培养系统是强大的工具,以迅速扩大我们对人类生物学的知识,并识别新的疾病治疗靶标。最近已显示生物工程骨骼肌,以重新承载原生肌肉生物学的许多特征。然而,目前的骨骼肌生物工程方法需要大量的细胞,试剂和劳动力,限制了它们对高通量研究的潜力。在此,我们使用小型化的96孔微肌平平台,以促进半自动组织形成,培养和分析人骨骼微肌(Hmμs)。利用迭代筛选方法,我们定义了一种无血清分化协议,该协议将人肌细胞的人肌细胞的快速,定向分化为骨骼肌纤维。得到的Hmμsms包括有组织的条纹和功能性Myofibres,其适当地响应电刺激。此外,我们开发了一种致灭绝的方法来长期刺激H mu m,以重新携带的锻炼训练的已知特征,包括Myofibre肥大和代谢蛋白的表达增加。我们的小型化方法携带,提供了一种新的平台,以实现人类骨骼肌生物学和运动生理学的高通量研究。

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