癌变·畸变·突变 ›› 2021, Vol. 33 ›› Issue (1): 6-11.doi: 10.3969/j.issn.1004-616x.2021.01.002

• 论著 • 上一篇    下一篇

PM2.5对HK-2肾细胞部分癌基因和凋亡基因表达的影响

李柏茹1,2, 秦双建1,2, 李闰冰2,3, 蔡颖2,3, 郑凯2,3, 王冰玉2,3, 曾明1, 肖芳1, 徐新云2   

  1. 1. 中南大学湘雅公共卫生学院, 湖南 长沙 410078;
    2. 深圳市疾病预防控制中心, 广东 深圳 518055;
    3. 南华大学公共卫生学院, 湖南 衡阳 421001
  • 收稿日期:2020-06-22 修回日期:2020-09-02 出版日期:2021-01-30 发布日期:2021-02-06
  • 通讯作者: 肖芳,E-mail:fangxiao@csu.edu.cn;徐新云,E-mail:xyxu2008@163.com E-mail:fangxiao@csu.edu.cn;xyxu2008@163.com
  • 作者简介:李柏茹,E-mail:15733295728@163.com。
  • 基金资助:
    深圳市科技研发项目(JCYJ20170413101713324,JCYJ20190807102205480)

Effects of PM2.5 exposure on expression of oncogenes and apoptosis genes in human renal epithelial cells

LI Boru1,2, QIN Shuangjian1,2, LI Runbing2,3, CAI Ying2,3, ZHENG Kai2,3, WANG Bingyu2,3, ZENG Ming1, XIAO Fang1, XU Xinyun2   

  1. 1. Xiangya School of Public Health, Central South University, Changsha 410078, Hunan;
    2. Shenzhen Center for Disease Control and Prevention, Shenzhen 518055, Guangdong;
    3. School of Public Health, University of South China, Hengyang 421001, Hunan, China
  • Received:2020-06-22 Revised:2020-09-02 Online:2021-01-30 Published:2021-02-06

摘要: 目的: 探讨PM2.5对人肾上皮细胞(HK-2)部分癌基因和凋亡基因表达的影响。方法: 利用CCK-8试剂盒测定PM2.5混悬液对HK-2细胞的半数抑制浓度(IC50);实验设阴性对照组、PM2.5混悬液低剂量(10 μg/mL)、高剂量(50 μg/mL)染毒组和阳性对照组(Cr6+ 10 μmol/L),分别对HK-2细胞处理24 h后利用实时荧光定量PCR (qPCR)和Western blot检测癌基因(c-mycc-fosp53)和凋亡基因(Caspase-8Caspase-9Bcl-2) mRNA和蛋白的表达水平。结果: PM2.5混悬液对HK-2细胞的IC50为95.98 μg/mL;经PM2.5混悬液染毒24 h,qPCR结果显示,与阴性对照组比较,PM2.5混悬液高剂量组和阳性对照组c-myc、c-fos、Caspase-8、Caspase-9 mRNA表达均升高,差异均有统计学意义(P < 0.01);p53和Bcl-2 mRNA表达降低,差异均有统计学意义(P < 0.01)。Western blot结果显示,与阴性对照组比较,PM2.5混悬液高剂量组和阳性对照组c-myc、c-fos、Caspase-8、Caspase-9蛋白表达均升高,差异均有统计学意义(P < 0.01);p53和Bcl-2蛋白表达均降低,差异均具有统计学意义(P < 0.05)。结论: PM2.5可引起HK-2细胞中部分癌基因表达上升、抑癌基因表达下降、促凋亡基因表达上升和抑凋亡基因表达下降,提示PM2.5对HK-2肾细胞部分癌基因和凋亡基因具有一定的促进与激活作用。

关键词: 大气细颗粒物, HK-2细胞, 癌基因, 凋亡基因

Abstract: OBJECTIVE: To investigate the effect of PM2.5 exposure on expression of oncogenes and apoptosis genes in human renal epithelial cells (HK-2). METHODS: The CCK8 assay was used to obtain the half maximal inhibitory concentration (IC50) of Taiyuan PM2.5 on human renal epithelial (HK-2) cells. HK-2 cells were treated with PM2.5 for 24 h. Four groups were set up:negative control group, low-dose PM2.5 group (10 μg/mL PM2.5), high-dose PM2.5 group (50 μg/mL PM2.5) and positive control group (Cr6+10 μmol/l). qPCR and Western blot were used to detect mRNA and proteins levels of apoptosis genes and oncogenes (c-myc, c-fos, p53, Caspase-8, Caspase-9 and Bcl-2). RESULTS: The IC50 value of Taiyuan PM2.5 on HK-2 cells was 95.98 μg/mL. After 24 hours of PM2.5 exposure, qPCR results show that, compared with the control group, expressions of c-myc, c-fos, Caspase-8, Caspase-9 mRNAs were significantly increased in the high-dose and positive control groups (P < 0.01). However, expressions of p53 and Bcl-2 mRNAs were significantly decreased in these two groups (P < 0.01). Western blot data show that, compared with the control group, expressions of c-myc, c-fos, Caspase-8, Caspase-9 proteins were significantly increased in the high-dose and positive control groups (P < 0.01). However, expressions of p53 and Bcl-2 proteins were significantly decreased in these two groups (P < 0.05). CONCLUSION: PM2.5 exposure to HK-2 cells increased the expression of oncogenes and apoptosis genes but decreased the expression of tumor suppressor and anti-apoptosis genes. Our results suggest that PM2.5 exposure can promote oncogenesis.

Key words: PM2.5, HK-2 cells, oncogenes, apoptosis genes

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