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药用植物来源的热休克蛋白化学诱导物与细胞保护基因反应。

Chemical inducers of heat shock proteins derived from medicinal plants and cytoprotective genes response.

机构信息

Division of Gastrointestinal Pathophysiology, Institute of Natural Medicine, University of Toyama, Toyama, Japan.

出版信息

Int J Hyperthermia. 2012;28(1):1-8. doi: 10.3109/02656736.2011.627408.

DOI:10.3109/02656736.2011.627408
PMID:22235779
Abstract

Environmental stress induces damage that activates an adaptive response in any organism. The cellular stress response is based on the induction of cytoprotective proteins, the so-called stress or heat shock proteins (HSPs). HSPs are known to function as molecular chaperones which are involved in the therapeutic approach of many diseases. Therefore in the current study we searched nontoxic chaperone inducers in chemical compounds isolated from medicinal plants. Screening of 80 compounds for their Hsp70-inducing activity in human lymphoma U937 cells was performed by western blotting. Five compounds showed significant Hsp70 up-regulation among them shikonin was most potent. Shikonin was able to induce Hsp70 at 0.1 µM after 3 h without activation of heat shock transcription factor 1 (HSF-1). It also induces significant reactive oxygen species generation. The expression level of genes responsive to shikonin was studied using global-scale microarrays and computational gene expression analysis tools. Significant increase in the nuclear factor erythroid 2-related factor 2 (Nrf2, NFEL2L2) -mediated oxidative stress response was observed that leads to the activation of HSP. The results of gene chip analysis were further confirmed by real-time qPCR assay. In short, the detailed mechanisms of Hsp70 induction by shikonin is not fully understood, Nrf2 and its target genes might be involved in the Hsp70 up-regulation in U937 cells.

摘要

环境压力会导致损伤,从而激活任何生物体的适应性反应。细胞应激反应基于诱导细胞保护蛋白,即所谓的应激或热休克蛋白(HSPs)。众所周知,HSPs 作为分子伴侣发挥作用,参与许多疾病的治疗方法。因此,在目前的研究中,我们从药用植物中分离的化学化合物中寻找非毒性伴侣诱导剂。通过蛋白质印迹法,筛选 80 种化合物对人淋巴瘤 U937 细胞中 Hsp70 诱导活性的影响。其中 5 种化合物显示出显著的 Hsp70 上调,其中紫草素最为有效。紫草素在 3 小时内以 0.1μM 的浓度诱导 Hsp70,而不激活热休克转录因子 1 (HSF-1)。它还诱导显著的活性氧生成。使用全基因组微阵列和计算基因表达分析工具研究了对紫草素响应的基因的表达水平。观察到核因子红细胞 2 相关因子 2 (Nrf2,NFEL2L2) 介导的氧化应激反应显著增加,导致 HSP 激活。基因芯片分析的结果进一步通过实时 qPCR 检测得到证实。简而言之,紫草素诱导 Hsp70 的详细机制尚不完全清楚,Nrf2 及其靶基因可能参与 U937 细胞中 Hsp70 的上调。

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