Amilon Karin R, Cortes-Araya Yennifer, Moore Benjamin, Lee Seungmee, Lillico Simon, Breton Amandine, Esteves Cristina L, Donadeu F Xavier
1 The Roslin Institute and R(D)SVS, University of Edinburgh , Edinburgh, United Kingdom .
2 The Euan Macdonald Centre for Motor Neurone Disease Research, University of Edinburgh , Edinburgh, United Kingdom .
Cell Reprogram. 2018 Oct;20(5):275-281. doi: 10.1089/cell.2018.0023. Epub 2018 Sep 12.
Induced pluripotent stem cells (iPSCs) have revolutionized human biomedicine through their use in disease modeling and therapy. In comparison, little progress has been made toward the application of iPSCs in veterinary species. In that regard, skeletal myocytes from iPSCs would have great potential for understanding muscle function and disease in the equine athlete. In this study, we generated skeletal myotubes by transducing equine iPSC-derived mesenchymal derivatives with an inducible lentiviral vector coding for the human sequence of the myogenic factor, MyoD. Myosin heavy chain-positive myotubes generated from two different iPSC lines were compared to myotubes from adult equine skeletal muscle progenitor cells (MPCs). iPSC myotubes had a smaller mean area than MPC myotubes (≤2-fold). In addition, quantitative polymerase chain reaction analyses showed that iPSC myotubes expressed MYH2 and MYH3 isoforms (at similar or lower levels than MPC myotubes), but they did not express the mature muscle isoform, MYH1. Compared to MPC myotubes, iPSC myotubes expressed reduced levels of the myogenic factors, MYOD1 and MYF6, but did not express MYF5. Finally, iPSC myotubes responded to KCl-induced membrane depolarization by releasing calcium and did so in a manner similar to MPC myotubes. In conclusion, this is the first study to report the generation of functional myocytes from equine iPSCs.
诱导多能干细胞(iPSC)通过用于疾病建模和治疗,给人类生物医学带来了变革。相比之下,iPSC在兽医物种中的应用进展甚微。在这方面,iPSC来源的骨骼肌细胞对于理解马运动员的肌肉功能和疾病具有巨大潜力。在本研究中,我们通过用编码生肌因子MyoD人类序列的可诱导慢病毒载体转导马iPSC来源的间充质衍生物,生成了骨骼肌管。将来自两个不同iPSC系的肌球蛋白重链阳性肌管与成年马骨骼肌祖细胞(MPC)的肌管进行了比较。iPSC肌管的平均面积小于MPC肌管(≤2倍)。此外,定量聚合酶链反应分析表明,iPSC肌管表达MYH2和MYH3亚型(水平与MPC肌管相似或更低),但不表达成熟肌肉亚型MYH1。与MPC肌管相比,iPSC肌管表达的生肌因子MYOD1和MYF6水平降低,但不表达MYF5。最后,iPSC肌管对KCl诱导的膜去极化有反应,通过释放钙,且方式与MPC肌管相似。总之,这是第一项报道从马iPSC生成功能性心肌细胞的研究。