首页> 外文期刊>The Journal of toxicological sciences >Hand1-Luc Embryonic Stem Cell Test (Hand1-Luc EST): A novel rapid and highly reproducible in vitro test for embryotoxicity by measuring cytotoxicity and differentiation toxicity using engineered mouse ES cells
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Hand1-Luc Embryonic Stem Cell Test (Hand1-Luc EST): A novel rapid and highly reproducible in vitro test for embryotoxicity by measuring cytotoxicity and differentiation toxicity using engineered mouse ES cells

机译:Hand1-Luc胚胎干细胞测试(Hand1-Luc EST):一种新型的快速,高度可重复的体外胚胎毒性测试,方法是使用工程化的小鼠ES细胞通过测量细胞毒性和分化毒性

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The embryonic stem cell test (EST) is a promising alternative method for evaluating embryotoxicity of test chemicals by measuring cytotoxicity and differentiation toxicity using mouse ES cells. Differentiation toxicity is analyzed by microscopically counting the beating of embryonic bodies after 10 days of culture. However, improvements are necessary to reduce the laborious manipulations involved and the time required to obtain results. We have previously reported the successful stable transfection of ES cells (ES-D3) with the heart and neural crest derivatives expressed transcript 1 (Hand1) gene and the establishment of a 96-well multi-plate-based new EST with luciferase reporter assay 6 days after treatment with test chemicals. Now, we propose an even more rapid and easier EST, named Hand1-Luc EST. We established another cell line to monitor the Hand1 gene expression via a luciferase reporter gene. By mRNA analysis and luciferase assay, we examined in detail the luciferase activity during cell differentiation, which allowed us to reduce the time of measurement from day 6 to day 5 (120 hr). Furthermore, the protocol was improved, with, among others, the measurement of cytotoxicity and differentiation toxicity taking place in the same 96-well round bottom plate instead of two different plates. With the positive control, 5-fluorouracil (5-FU), and 9 test chemicals, data with high reproducibility and very low variation (CV
机译:胚胎干细胞测试(EST)是一种有前途的替代方法,可通过使用小鼠ES细胞测量细胞毒性和分化毒性来评估测试化学品的胚胎毒性。培养10天后,通过显微镜计数胚体的跳动来分析分化毒性。但是,必须进行改进以减少所涉及的繁琐操作和减少获得结果所需的时间。我们以前曾报道过用心脏和神经c衍生物表达的转录物1(Hand1)基因成功稳定转染ES细胞(ES-D3),并建立了基于96孔多板荧光素酶报道基因的新型EST。用测试化学品处理后的几天。现在,我们提出一个更快速,更轻松的EST,称为Hand1-Luc EST。我们建立了另一种细胞系,通过荧光素酶报告基因来监测Hand1基因的表达。通过mRNA分析和萤光素酶测定,我们详细检查了细胞分化过程中的萤光素酶活性,这使我们能够将测量时间从第6天减少到第5天(120小时)。此外,该方案得到了改进,其中包括在相同的96孔圆形底板中而不是在两个不同的板上进行细胞毒性和分化毒性的测量。使用阳性对照,5-氟尿嘧啶(5-FU)和9种测试化学品,数据具有高重现性和极低的变异性(CV

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