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中国科学院大学学报 ›› 2009, Vol. 26 ›› Issue (1): 83-90.DOI: 10.7523/j.issn.2095-6134.2009.1.012

• 论文 • 上一篇    下一篇

纳米氧化锌对人肺腺癌细胞A549的毒性

王琳 王莉娟 张芳 丁文军   

  1. 中国科学院研究生院生命科学学院,北京100049
  • 收稿日期:1900-01-01 修回日期:1900-01-01 发布日期:2009-01-15

Cytotoxicity of ZnO nanoparticles in human lung cancer cell lines A549

WANG Lin , WANG Li-juan , ZHANG Fang , DING Wen-jun   

  1. College of Life Sciences, Graduate University of the Chinese Academy of Sciences, Beijing 100049 , China
  • Received:1900-01-01 Revised:1900-01-01 Published:2009-01-15

摘要: 探讨纳米氧化锌(ZnO)对体外培养的人肺腺癌细胞A549的生物学效应。使用原子力显微镜(AFM)、透射电镜(TEM)和X射线衍射仪(XRD)研究纳米ZnO颗粒物的理化性质。然后,使用0mmol/L、0.1mmol/L、0.5mmol/L、1mmol/L、5mmol/L、10mmol/L的纳米ZnO处理体外培养的人肺腺癌A549细胞,MTT 法测定细胞生长活性。并且测定1mmol/L 纳米ZnO染毒24h后细胞培养液上清中,乳酸脱氢酶(LDH)和胞内的超氧化物歧化酶(SOD)、过氧化氢酶(CAT)的活性以及丙二醛(MDA)的含量。使用透射电镜和流式细胞仪检测细胞凋亡的情况。荧光染色检测细胞产生活性氧(ROS)的生成。实验所用的ZnO纳米颗粒为长75 nm、直径20nm的针状纤锌矿晶体。细胞实验结果表明,纳米ZnO颗粒对A549细胞的生长活性具有明显的抑制作用,存在剂量-效应关系。培养液上清中LDH活性显著升高(P < 0.05),胞内CAT活性显著下降、MDA含量显著升高(P < 0.01),但SOD活性下降不明显。荧光染色检测发现染毒后A549细胞出现细胞凋亡,而且细胞内ROS的生成与纳米ZnO存在剂量-效应关系。结论是纳米氧化锌诱导人肺腺癌A549细胞产生活性氧,引发细胞凋亡,并产生细胞毒性。

关键词: 纳米氧化锌, 人肺腺癌A549细胞, 细胞毒性

Abstract: The aim of the study was to investigate the toxic effects of nanosized ZnO in vitro. Characterization of ZnO nanoparticles was carried out by atomic force microscope (AFM), transmission electron microscope (TEM) and X-ray diffraction (XRD). In this study, lung cancer cell lines A549 were exposed to 0mmol/L, 0.1mmol/L, 0.5mmol/L, 1mmol/L, 5mmol/L, 10mmol/L of ZnO nanoparticles, respectively. MTT assay was performed to evaluate the viabilities of ZnO-treated cells after 12h, 24h, 36h and 48h exposure. The activities of lactate dehydrogenase (LDH), cellular superoxide dismutase (SOD), catalase (CAT), and malondialdehyde (MDA) were determined after exposure to 1mmol/L ZnO for 24 h. Moreover, apoptotic characteristics and reactive oxygen species (ROS) production in A549 cells were measured. ZnO nanoparticles were needlelike crystals (75 nm length; 20 nm diameter). The viability of A549 cells were reduced after exposure to ZnO nanoparticles in a dose-dependent manner. The activities of LDH and the levels of MDA were significantly increased (P < 0.05, P < 0.01), respectively. However, the activities of CAT were significantly decreased (P < 0.01). No significant difference in the activities of SOD was observed between the ZnO-treated cells and the controls. ZnO nanoparticles at 1mmol/L induced apoptosis in A549 cells. The levels of ROS in ZnO-treated cells were significantly higher than that in controls. These results suggested that ZnO nanoparticles could result in apoptosis in A549 cells through oxidative stress.

Key words: ZnO nanoparticles, human lung cancer cell lines A549, cytotoxicity