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Development of the excitation-contraction coupling machinery and its relation to myofibrillogenesis in human iPSC-derived skeletal myocytes

机译:激发-收缩偶联机制的发展及其与人iPSC衍生的骨骼肌细胞肌原纤维形成的关系

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摘要

BackgroundHuman induced pluripotent stem cells-derived myogenic progenitors develop functional and ultrastructural features typical of skeletal muscle when differentiated in culture. Besides disease-modeling, such a system can be used to clarify basic aspects of human skeletal muscle development. In the present study, we focus on the development of the excitation-contraction (E-C) coupling, a process that is essential both in muscle physiology and as a tool to differentiate between the skeletal and cardiac muscle. The occurrence and maturation of E-C coupling structures (Sarcoplasmic Reticulum-Transverse Tubule (SR-TT) junctions), key molecular components, and Ca2+ signaling were examined, along with myofibrillogenesis.
机译:背景人类诱导的多能干细胞来源的成肌祖细胞在培养中分化时会发展出典型的骨骼肌功能和超微结构特征。除了疾病建模之外,这种系统还可以用于阐明人类骨骼肌发育的基本方面。在本研究中,我们专注于兴奋收缩(E-C)耦合的开发,该过程在肌肉生理学中是必不可少的,并且是区分骨骼肌和心肌的工具。研究了E-C偶联结构(浆质网-横管(SR-TT)连接),关键分子成分和Ca 2 + 信号的发生和成熟,以及肌原纤维形成。

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