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Comparative study of directional differentiation of human and mouse embryonic stem cells into cardiomyocytes

机译:人和小鼠胚胎干细胞定向分化为心肌细胞的比较研究

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This comparative study investigates the method, efficiency, and anti-hypoxic ability of cardiomyocytes, directionally induced from human (h) and mouse (m) embryonic stem cells (ESCs). hESCs were induced into cardiomyocytes by suspension culture, without inducers, or adherent culture using the inducers activin A and BMP4. mESCs were induced into cardiomyocytes by hanging-drop method, without inducers or induced with vitamin C. All four methods successfully induced ESCs to differentiate into cardiomyocytes. There was a significant difference between groups with and without inducers. A significant difference was found between mESC and hESC groups with inducers. The average beating frequency of cardiomyocytes differentiated from hESC was lower than cardiomyocytes differentiated from mESC, while the average beating frequency of cardiomyocytes differentiated from the same cell line, despite different culture methods, did not differ. Beating cardiomyocytes of each group were positive for cTnT staining. Spontaneous action potentials of beating cardiomyocytes were detected by patch-clamp experiments in each group. Different apoptotic ratios were detected in beating cardiomyocytes in each group and the difference between cardiomyocytes induced from mESCs and hESCs was statistically significant. The differentiation efficiencies in the groups without inducers were significantly higher than those without inducers. The induction of mESCs was more simple and efficient compared with hESCs. Without the presence of other protective factors, the anti-hypoxic ability of cardiomyocytes induced from hESCs was stronger and the beating times were longer in vitro compared with mESCs.
机译:这项比较研究调查了从人类(h)和小鼠(m)胚胎干细胞(ESC)定向诱导的心肌细胞的方法,效率和抗缺氧能力。通过不使用诱导剂的悬浮培养或使用诱导剂激活素A和BMP4的贴壁培养将hESC诱导为心肌细胞。通过悬滴法将mESCs诱导为心肌细胞,无诱导剂或维生素C诱导。所有四种方法均成功诱导ESCs分化为心肌细胞。有和没有诱导剂的组之间存在显着差异。在具有诱导物的mESC和hESC组之间发现了显着差异。从hESC分化出的心肌细胞的平均跳动频率低于从mESC分化出的心肌细胞,而从同一细胞系分化出的心肌细胞的平均跳动频率,尽管培养方法不同,但没有差异。每组跳动的心肌细胞的cTnT染色均为阳性。通过膜片钳实验在每组中检测跳动的心肌细胞的自发动作电位。在每组跳动的心肌细胞中检测到不同的凋亡率,并且mESCs和hESCs诱导的心肌细胞之间的差异具有统计学意义。没有诱导剂的组的分化效率显着高于没有诱导剂的组。与hESC相比,mESC的诱导更加简单有效。在没有其他保护因子的情况下,与mESCs相比,hESCs诱导的心肌细胞的抗缺氧能力更强,跳动时间更长。

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