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张瑜, 肖纯凌, 杨丹, 石威. PM2.5暴露对肺组织和H1299细胞Twist1、Zeb1表达影响[J]. 中国公共卫生, 2020, 36(7): 1010-1013. DOI: 10.11847/zgggws1120346
引用本文: 张瑜, 肖纯凌, 杨丹, 石威. PM2.5暴露对肺组织和H1299细胞Twist1、Zeb1表达影响[J]. 中国公共卫生, 2020, 36(7): 1010-1013. DOI: 10.11847/zgggws1120346
Yu ZHANG, Chun-ling XIAO, Dan YANG, . Inhibited proliferation and abnormal expression of Twist1, Zeb1 in rat lung tissues and H1299 cells induced by PM2.5 exposure[J]. Chinese Journal of Public Health, 2020, 36(7): 1010-1013. DOI: 10.11847/zgggws1120346
Citation: Yu ZHANG, Chun-ling XIAO, Dan YANG, . Inhibited proliferation and abnormal expression of Twist1, Zeb1 in rat lung tissues and H1299 cells induced by PM2.5 exposure[J]. Chinese Journal of Public Health, 2020, 36(7): 1010-1013. DOI: 10.11847/zgggws1120346

PM2.5暴露对肺组织和H1299细胞Twist1、Zeb1表达影响

Inhibited proliferation and abnormal expression of Twist1, Zeb1 in rat lung tissues and H1299 cells induced by PM2.5 exposure

  • 摘要:
      目的  探讨细颗粒物(PM2.5)暴露对大鼠肺组织及H1299细胞中Zeb1、Twist1的表达和细胞增殖影响。
      方法  体内实验:40只大鼠分别给予PM2.5混悬液和生理盐水,于暴露后2和4周收集肺组织;体外实验:分别用0、50、100、200 μg/mL PM2.5混悬液培养H1299细胞48 h,收集细胞;采用免疫印迹法法检测小鼠肺组织和H1299细胞中Zeb1、Twist1蛋白表达,采用噻唑蓝(MTT)法检测H1299细胞增殖率。
      结果  体内实验:与对照组(0.68 ± 0.19)、(0.99 ± 0.11)比较,PM2.5暴露大鼠4周后肺组织中Zeb1、Twist1蛋白表达量分别为(0.27 ± 0.18)(0.44 ± 0.15)明显下调(P < 0.05)。体外实验:与对照组(1.34 ± 0.38)、(1.05 ± 0.11)比较,200 μg/mL PM2.5染毒组H1299细胞中Zeb1、Twist1蛋白表达量分别为(0.17 ± 0.08)、(0.20 ± 0.05)明显下调(P < 0.05);200 μg/mL PM2.5处理H1299细胞72 h,H1299细胞生存率为(25.26 ± 1.84)%,明显低于对照组(P < 0.05)。
      结论  PM2.5暴露后,小鼠肺组织及人肺腺癌细胞H1299中Zeb1、Twist1表达明显降低,并且肺癌细胞(H1299)呈现增殖抑制现象。

     

    Abstract:
      Objective  To investigate the effect of exposure to particulate matter ≤ 2.5 μm in aerodynamic diameter (PM2.5) on the expression of zinc finger E-box binding homeobox 1 (Zeb1) and Twist1 and cell proliferation in rat lung and H1299 cells.
      Methods  Totally 40 Wistar rats were treated with PM2.5 suspension and normal saline 6 hours per day and 6 days per week for 2 and 4 weeks; then lung tissues of the rats were collected. The H1299 cells were cultured in suspension mixed with PM2.5 at the dosages of 0, 50, 100, 200 μg/mL for 48 hours. The expression of Zeb1 and Twist1 protein in the rats' lung tissues and H1299 cells were detected with immunoblotting. The proliferation rate of H1299 cells was detected with methyl thiazolyl tetrazolium (MTT) assay.
      Results  The Zeb1 and Twist1 protein (0.27 ± 0.18 and 0.44 ± 0.15) in lung tissues of the rats exposed to PM2.5 for 4 weeks were significantly down-regulated compared to those in control rats (0.68 ± 0.19 and 0.99 ± 0.11) (both P < 0.05). Significantly down-regulated expression of Zeb1 and Twist1 protein (0.17 ± 0.08 and 0.20 ± 0.05) were also observed in H1299 cells cultured with 200 μg/mL PM2.5 suspension in comparison with those (1.34 ± 0.38 and 1.05 ± 0.11) in control cells (both P < 0.05); in addition, the survival rate (25.26 ± 1.84%) of H1299 cells cultured with 200 μg/mL PM2.5 suspension for 72 hours was significantly lower than that of the control cells (P < 0.05).
      Conclusion  PM2.5 exposure could decrease the expression of Zeb1 and Twist1 in rats' lung tissues and human lung adenocarcinoma H1299 cells and inhibit the proliferation of the H1299 cells.

     

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