Jiang Jiong, Dong Lei, Qin Bin, Guo Xiaoyan, Li Hong, Shi Haitao, Liu Yaping
Department of Gastroenterology, Second Affiliated Hospital, Xi'an Jiaotong University College of Medicine, Xi'an 710004, China. E-mail:
Nan Fang Yi Ke Da Xue Xue Bao. 2014 Nov;34(11):1606-10.
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.
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.
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.
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.
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。
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。
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。
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。