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Improvement in Sensitivity of Live Cell-Based Sensor Cells by Co-Transfection of a Reporter Gene Driven by a Modified HSP70B' and HSF1Expression Vector

机译:通过转染修饰的HSP70B'和HSF1表达载体驱动的报告基因的共转染,提高基于活细胞的传感器细胞的敏感性。

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We previously reported that live cells transfected with a luciferase construct carrying the HSP70B' gene promoterincreases the luciferase activity in response to toxic reagents and can be used as an intelligent cytotoxicity sensordevice (i.e., sensor cells). In the present study, in order to improve the sensitivity of these cytotoxic sensor cells, we cotransfectedthe sensor cells with both the luciferase construct carrying the HSP70B' gene promoter (pMCREx3) and anHSF1 expression vector driven by a modified HSP70B’ promoter (pCRE/HSF). Cells co-transfected with pMCREx3 andpCRE/HSF showed 2.5 times higher sensitivity for CdCl2 cytotoxicity than cells transfected with pMCREx3 alone, indicatingthat sensor cells co-transfected in this way are useful and sensitive tools with which to detect a cytotoxic response.
机译:我们以前曾报道过,用携带HSP70B'基因启动子的萤光素酶构建体转染的活细胞可响应有毒试剂而提高萤光素酶的活性,并可用作智能细胞毒性传感器设备(即传感器细胞)。在本研究中,为了提高这些细胞毒性传感器细胞的敏感性,我们用携带HSP70B'基因启动子(pMCREx3)的萤光素酶构建体和由修饰的HSP70B'启动子驱动的anHSF1表达载体(pCRE / HSF)共转染了传感器细胞)。用pMCREx3和pCRE / HSF共转染的细胞对CdCl2细胞毒性的敏感性比仅用pMCREx3转染的细胞高2.5倍,这表明以这种方式共转染的传感器细胞是检测细胞毒性反应的有用且灵敏的工具。

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