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Comparison of 10 Control hPSC Lines for Drug Screening in an Engineered Heart Tissue Format

机译:一种控制HPSC线路在工程心脏组织形式中的药物筛选中的比较

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Human-induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CM) are commercially available, and cardiac differentiation established routine. Systematic evaluation of several control hiPSC-CM is lacking. We investigated 10 different control hiPSC-CM lines and analyzed function and suitability for drug screening. Five commercial and 5 academic hPSC-CM lines were casted in engineered heart tissue (EHT) format. Spontaneous and stimulated EHT contractions were analyzed, and 7 inotropic indicator compounds investigated on 8 cell lines. Baseline contractile force, kinetics, and rate varied widely among the different lines (e.g., relaxation time range: 118-471?ms). In contrast, the qualitative correctness of responses to BayK-8644, nifedipine, EMD-57033, isoprenaline, and digoxin in terms of force and kinetics varied only between 80% and 93%. Large baseline differences between control cell lines support the request for isogenic controls in disease modeling. Variability appears less relevant for drug screening but needs to be considered, arguing for studies with more than one line.
机译:人诱导的多能干细胞衍生的心肌细胞(HIPSC-CM)是可商购的,并且心脏分化成熟的常规。缺乏对几种控制髋关节CM的系统评估。我们调查了10种不同的控制HIPSC-CM系列,分析了药物筛选的功能和适用性。五种商业和5个学术HPSC-CM系列被铸造在工程心脏组织(EHT)格式。分析了自发性和刺激的EHT收缩,并在8个细胞系上研究了7种官能指示剂化合物。基线收缩力,动力学和速率在不同的线条之间广泛变化(例如,放松时间范围:118-471?MS)。相比之下,对Bayk-8644,NifeDipine,EMD-57033,异丙肾上腺素和高辛的反应的定性正确性在力和动力学方面不同于80%至93%。对照细胞系之间的大基线差异支持疾病建模中的同质对照的要求。可变异性对药物筛查似乎不如需要考虑,但争论以以上的线路进行研究。

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