癌变·畸变·突变 ›› 2022, Vol. 34 ›› Issue (2): 93-97.doi: 10.3969/j.issn.1004-616x.2022.02.003

• 论著 • 上一篇    

N-乙酰半胱氨酸对纳米二氧化钛诱发细胞遗传损伤的保护作用

王晗1,2, 周滔1,2, 徐云东1, 郭锡汉1,2, 倪娟1,2, 汪旭1,2   

  1. 1. 云南师范大学生命科学学院, 云南 昆明 650500;
    2. 云南师范大学生物能源持续开发与利用教育部工程研究中心, 云南 昆明 650500
  • 收稿日期:2021-08-23 修回日期:2021-12-02 发布日期:2022-04-07
  • 通讯作者: 汪旭,E-mail:wangxu@fudan.edu.cn E-mail:wangxu@fudan.edu.cn
  • 作者简介:王晗,E-mail:wanghan9215@163.com。
  • 基金资助:
    国家自然科学基金(31860301,31900410);云南省教育厅科研基金项目(2020J0089);云南师范大学博士启动基金项目

Protective effects of N-acetylcysteine on genotoxicity induced by titanium dioxide nanoparticles in vitro

WANG Han1,2, ZHOU Tao1,2, XU Yundong1, GUO Xihan1,2, NI Juan1,2, WANG Xu1,2   

  1. 1. School of Life Sciences, Yunnan Normal University, Kunming 650500;
    2. Engineering Research Center of Sustainable Development and Utilization of Biomass Energy, Ministry of Education, Yunnan Normal University, Kunming 650500, Yunnan, China
  • Received:2021-08-23 Revised:2021-12-02 Published:2022-04-07

摘要: 目的:探讨抗氧化剂N-乙酰半胱氨酸(NAC)对纳米二氧化钛(TiO2-NPs)诱发人正常肝细胞L-02和肺细胞HBE遗传损伤的保护作用。方法:分别将对数生长期的L-02和HBE细胞分为3组,即正常培养的对照组、TiO2-NPs(80μg/mL)暴露组、TiO2-NPs(80μg/mL)与NAC(20μmol/L)联合暴露组;各组细胞处理72h后,采用H2O2试剂盒检测细胞内H2O2浓度;实时荧光定量(qPCR)法检测L-02、HBE细胞端粒长度(TL)的改变;胞质分裂阻断微核细胞组试验(CBMN-Cyt)评估受试细胞的染色体不稳定性(CIN)及细胞死亡率。结果:与对照组相比,TiO2-NPs暴露72h后,可诱导L-02和HBE细胞内H2O2浓度显著升高(P<0.05),致使L-02和HBE细胞TL缩短、CIN增加、细胞死亡率增加(P<0.05);当TiO2-NPs与NAC联合暴露72h后时,两种受试细胞的H2O2水平和CIN仍较对照组显著升高(P<0.05),而TL和细胞死亡率与对照组间的差异均无统计学意义(P>0.05);与单独暴露TiO2-NPs组相比,联合暴露时两种受试细胞的TL显著增加(P<0.05),且CIN及细胞死亡率显著降低(P<0.05)。结论:抗氧化剂NAC可抑制TiO2-NPs诱发的人肝细胞L-02和肺细胞HBE的TL缩短和细胞死亡,维护染色体稳定,对细胞有一定保护作用。

关键词: N-乙酰半胱氨酸, 纳米二氧化钛, 端粒, 遗传损伤, 保护作用

Abstract: OBJECTIVE: To investigate protective effects of N-acetylcysteine (NAC) on genotocicity induced by titanium dioxide nanoparticles (TiO2-NPs) in human normal hepatocytes L- 02 and human normal lung epithelial cells HBE. METHODS:L-02 and HBE cells grown in log phase were divided into 3 groups: control group (normal culture),TiO2-NPs exposed group (80 μg/mL),and TiO2-NPs (80 μg/mL) and NAC (20 μmol/L) co-exposed group. After the cells in each group were exposed for 72 h,H2O2 kit was used to detect the intracellular H2O2 level; telomere length (TL) of L-02 and HBE cells in each group was measured by realtime quantitative PCR; chromosomal instability (CIN) and cell death indexes were evaluated by cytokinesisblock micronucleus cytome assay (CBMN-Cyt). RESULTS: Compared with the control group, TiO2-NPs exposed for 72 h significantly increased intracellular H2O2 levels in L-02 and HBE cells (P<0.05),resulting in shortened TL,increased CIN and cell death (P<0.05). When co-exposed with TiO2-NPs and NAC for 72 h, the H2O2 levels and CIN among the two types cells were significantly higher than those of the control group (P< 0.05),while TL and cell death had no significant differences compared with the control group (P>0.05). When compared with the TiO2-NPs group,increased TL (P<0.05),decreased CIN,and decreased cell death rates were found in TiO2-NPs and NAC co-exposed group (both P<0.05). CONCLUSION: The antioxidant NAC strongly reduced the telomere shortening and cell death induced by TiO2-NPs in L- 02 and HBE cells, showing the effects of protecting cells under the stress of TiO2-NPs.

Key words: N-acetylcysteine, titanium dioxide nanoparticles, telomere, genetic damage, protective effect

中图分类号: