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100mT SMF 对热休克/荧光素酶报告基因系统中 hsp70 启动子激活的影响。

The effect of 100 mT SMF on activation of the hsp70 promoter in a heat shock/luciferase reporter system.

机构信息

Imaging Program, Lawson Health Research Institute, London, Ontario, Canada.

出版信息

J Cell Biochem. 2009 Nov 1;108(4):956-62. doi: 10.1002/jcb.22327.

DOI:10.1002/jcb.22327
PMID:19725048
Abstract

Human exposure to magnetic fields, increased through use of new technologies like magnetic resonance imaging (MRI), has prompted investigations into possible effects of static magnetic fields (SMFs) on cellular processes. However, controversy still remains between many studies, which likely results from a lack of uniformity across experimental parameters, including the length of magnetic field exposure, the strength of the magnetic field, and the cell type or organism under investigation. The purpose of this research was to monitor effects of SMF exposure using real-time luminescence photometry. The study investigated the potential interaction of a 100 mT SMF on a heat shock protein (hsp70)/luciferase reporter construct in stably transfected NIH3T3 cells. Changes in heat shock promoter activation following 100 mT SMF exposure were analyzed and detected as bioluminescence in real-time. Two heat parameters were considered in combination with sham- and 100 mT-exposed experiments: no heat or 1,800 s heat. As expected, there was a significant increase in bioluminescence in response to 1,800 s of heat alone. However, no significant difference in average hsp70 promoter activation between sham and 100 mT experiments was observed for no heat or 1,800 s heat experiments. Therefore, a 100 mT SMF was shown to have no effect on the activation of the heat shock protein promoter during SMF exposure or when SMF exposure was combined with a heat insult.

摘要

人类接触磁场的机会因磁共振成像(MRI)等新技术的应用而增加,这促使人们研究静磁场(SMF)对细胞过程可能产生的影响。然而,许多研究之间仍然存在争议,这可能是由于实验参数缺乏一致性造成的,包括磁场暴露的时间长度、磁场的强度以及正在研究的细胞类型或生物体。本研究旨在使用实时发光光度法监测 SMF 暴露的影响。该研究调查了 100 mT SMF 对稳定转染的 NIH3T3 细胞中热休克蛋白(hsp70)/荧光素酶报告基因构建体的潜在相互作用。分析了 100 mT SMF 暴露后热休克启动子激活的变化,并实时检测生物发光。在假暴露和 100 mT 暴露实验中,结合两个热参数进行了分析:无热或 1800 s 热。正如预期的那样,单独 1800 s 的热刺激会显著增加生物发光。然而,在无热或 1800 s 热刺激实验中,未观察到 sham 和 100 mT 实验之间 hsp70 启动子激活的平均差异。因此,100 mT SMF 显示在 SMF 暴露期间或 SMF 暴露与热损伤结合时,对热休克蛋白启动子的激活没有影响。

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