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A transformed fish cell line expressing a green fluorescent protein-luciferase fusion gene responding to cellular stress

机译:表达绿色荧光蛋白-荧光素酶融合基因的转化鱼细胞系响应细胞应激

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摘要

We obtained a stable transformed fish (EPC) cell line containing a reporter gene under the control of the tilapia HSP70 promoter. Expression of the reporter gene, coding for a green fluorescent protein (GFP)-luciferase fusion protein, was assessed by measuring the luciferase enzymatic activity by luminometry and the GFP expression by fluorescence microscopy and flow cytometry. The clone was characterized for its capacity to respond to heat shock treatment. The results show high induction after 1 h at 37 degrees C of treatment, up to 500-fold. In addition, its convenience to detect a large range of cellular stressors was evaluated. We observed high induction when Cd2+, Zn2+, Hg2+ or Cu2+ was added, but not Pb2+. In addition, activation of the reporter gene was observed in the presence of other compounds such as acetyl chloride, tetrachlorophenol, chloroacetamide and sodium arsenite. In conclusion, this cell line can be used as a rapid, cheap and easy biological test to determine cellular stress induced by environmental pollutants, alone or in conjunction with other, more specific assays.
机译:我们获得了一个稳定的转化鱼(EPC)细胞系,该细胞系包含在罗非鱼HSP70启动子控制下的报告基因。编码绿色荧光蛋白(GFP)-荧光素酶融合蛋白的报告基因的表达通过光度法测量荧光素酶的酶活性以及通过荧光显微镜和流式细胞术评估GFP的表达来评估。该克隆的特征在于其对热激处理的响应能力。结果显示,在37摄氏度的温度下处理1 h后,诱导强度最高,达到500倍。另外,评估了其检测大范围细胞应激源的便利性。当添加Cd2 +,Zn2 +,Hg2 +或Cu2 +而不添加Pb2 +时,我们观察到高诱导。另外,在其他化合物例如乙酰氯,四氯苯酚,氯乙酰胺和亚砷酸钠的存在下观察到报告基因的活化。总之,该细胞系可单独或与其他更具体的测定法一起用作测定环境污染物诱导的细胞应激的快速,廉价和简便的生物学测试。

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