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[胃癌细胞系中Toll样受体7的表达及TLR7激动剂对SGC-7901细胞体外增殖和凋亡的影响]

[Expression of Toll-like receptor 7 in gastric cancer cell lines and effects of TLR7 agonist on proliferation and apoptosis of SGC-7901 cells in vitro].

作者信息

Jiang Jiong, Dong Lei, Qin Bin, Guo Xiaoyan, Li Hong, Shi Haitao, Liu Yaping

机构信息

Department of Gastroenterology, Second Affiliated Hospital, Xi'an Jiaotong University College of Medicine, Xi'an 710004, China. E-mail:

出版信息

Nan Fang Yi Ke Da Xue Xue Bao. 2014 Nov;34(11):1606-10.

Abstract

OBJECTIVE

To investigate the expression of Toll-like receptor 7 (TLR7) in gastric cancer cell lines and the effect of imiquimod, a TLR7 agonist, on the proliferation and apoptosis of SGC-7901 cells.

METHODS

The protein expression levels of TLR7 were detected with Western blotting in 3 human gastric cancer cell lines (SGC-7901, HGC-27 and MKN-28). The cell line expressing the highest TLR7 level was exposed to different doses of imiquimod for 12-72 h and the cell viability was assessed with MTT assay. The cell apoptosis rate after 100 µg/ml imiquimod treatment for 12 or 24 h was quantified by flow cytometry, and the ultrastructual changes of the cells were observed under electron microscope. The expression of apoptosis-related genes Bcl-2 and Bax were analyzed with real-time PCR.

RESULTS

All the 3 cell lines expressed TLR7, among which SGC-7901 cells showed the highest expression level. TLR7 agonist imiquimod dose- and time-dependently reduced the viability of SGC-7901 cells. Exposure to 100 µg/ml imiquimod for 24 h resulted in SGC-7901 cell apoptosis as shown by an increased ratio of early apoptotic cells and significant ultrastructural changes of the cells. Real-time PCR demonstrated that imiquimod treatment for 24 h caused a dose-dependent reduction of Bcl-2 mRNA expression and increment of Bax mRNA expression.

CONCLUSIONS

TLR7 protein is expressed in all the 3 gastric cancer lines and its agonist imiquimod can inhibit cell proliferation and induce apoptosis in SGC-7901 cells.

摘要

目的

研究Toll样受体7(TLR7)在胃癌细胞系中的表达情况,以及TLR7激动剂咪喹莫特对SGC-7901细胞增殖和凋亡的影响。

方法

采用蛋白质免疫印迹法检测3种人胃癌细胞系(SGC-7901、HGC-27和MKN-28)中TLR7的蛋白表达水平。将TLR7表达水平最高的细胞系暴露于不同剂量的咪喹莫特中12 - 72小时,并用MTT法评估细胞活力。采用流式细胞术定量检测100μg/ml咪喹莫特处理12或24小时后的细胞凋亡率,并在电子显微镜下观察细胞的超微结构变化。通过实时聚合酶链反应分析凋亡相关基因Bcl-2和Bax的表达。

结果

3种细胞系均表达TLR7,其中SGC-7901细胞的表达水平最高。TLR7激动剂咪喹莫特可剂量和时间依赖性地降低SGC-7901细胞的活力。暴露于100μg/ml咪喹莫特24小时导致SGC-7901细胞凋亡,表现为早期凋亡细胞比例增加和细胞超微结构显著变化。实时聚合酶链反应表明,咪喹莫特处理24小时导致Bcl-2 mRNA表达剂量依赖性降低和Bax mRNA表达增加。

结论

TLR7蛋白在所有3种胃癌细胞系中均有表达,其激动剂咪喹莫特可抑制SGC-7901细胞的增殖并诱导其凋亡。

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