高温高温相容β -内酰胺酶转录报告基因试验探讨热休克反应途径。

Michael K Hancock, Menghang Xia, Elizabeth S Frey, Srilatha Sakamuru, Kun Bi
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引用次数: 6

摘要

已知适度的环境和生理应激源可启动保护性热休克反应(HSR),导致细胞存活。热休克在很大程度上是由热休克因子(HSF)的激活介导的,导致热休克蛋白的表达增加。高铁信号的失调与多种疾病有关,包括癌症、炎症和神经退行性疾病。可以调节HSR的化合物已被用于治疗这些疾病。为了促进HSR调节剂的发现,我们开发了一种高通量可调节β -内酰胺酶转录报告基因检测方法来监测HSF的功能。在HSP70基因启动子中的HSF反应元件(HSE)的控制下,对HeLa细胞进行工程化,使其表达β -内酰胺酶报告基因。利用hsf特异性sirna和已知的小分子调节剂,验证了hsf - β -内酰胺酶(HSE-bla)报告基因测定。利用荧光共振能量转移(FRET)为基础的细胞可渗透的betalactamase底物,该实验可以小型化到1536孔格式。我们的结果表明,该分析是稳健的,可以应用于高通量筛选(HTS)的HSR调节剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

HTS-compatible beta-lactamase transcriptional reporter gene assay for interrogating the heat shock response pathway.

HTS-compatible beta-lactamase transcriptional reporter gene assay for interrogating the heat shock response pathway.

HTS-compatible beta-lactamase transcriptional reporter gene assay for interrogating the heat shock response pathway.

HTS-compatible beta-lactamase transcriptional reporter gene assay for interrogating the heat shock response pathway.

Moderate environmental and physiological stressors are known to initiate protective heat shock response (HSR) leading to cell survival. HSR is largely mediated by the activation of heat shock factor (HSF), resulting in increased heat shock protein expression. Dysregulation of the HSR signaling has been associated with various diseases including cancer, inflammation and neurodegenerative disorders. Compounds that can modulate HSR have been pursued for the treatment of these diseases. To facilitate the discovery of HSR modulators, we developed a high-throughput amenable betalactamase transcriptional reporter gene assay for monitoring the function of HSF. HeLa cells were engineered to express the beta-lactamase reporter under the control of HSF response elements (HSE) present in the HSP70 gene promoter. The HSE-beta lactamase (HSE-bla) reporter gene assay was validated by using HSF-specific siRNAs and known small molecule modulators. Taking the advantage of fluorescence resonance energy transfer (FRET)-based cell permeable betalactamase substrate, this assay can be miniaturized into 1536-well format. Our results demonstrate that the assay is robust and can be applied to high-throughput screening (HTS) for modulators of HSR.

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