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作 者:李艳博[1] 张海霞[2] 郭彩霞[1] 金明华[3] 于永波[1] 黄沛力[1] 孙志伟[1,3]
机构地区:[1]首都医科大学公共卫生与家庭医学学院,北京100069 [2]北京市朝阳区疾病预防控制中心,北京100021 [3]吉林大学公共卫生学院卫生毒理学教研室,吉林长春130021
出 处:《吉林大学学报(医学版)》2012年第3期495-500,I0002,共7页Journal of Jilin University:Medicine Edition
基 金:北京市教育委员会创新团队项目资助课题(PHR201107116);北京市属高等学校人才强教深化计划项目资助课题(PHR201006110)
摘 要:目的:研究巯基乙酸(TGA)包覆的碲化镉(CdTe)量子点(QDs)对人正常肝HL-7702细胞的毒性和DNA损伤的作用,为QDs毒理学研究和安全性评价提供实验依据。方法:实验设立对照组和不同浓度CdTeQDs作用组(浓度分别为6.25、12.50、25.00和50.00mg.L-1)。CdTe QDs作用于HL-7702细胞后,分别采用MTT法检测细胞增殖变化,单细胞凝胶电泳法(SCGE)检测细胞DNA损伤情况,PI单染流式细胞术(FCM)检测细胞周期变化,AO/EB双荧光染色法和AnnexinⅤ-FITC/PI双染FCM检测细胞凋亡情况。结果:MTT法,CdTe QDs可抑制HL-7702细胞增殖,并存在剂量-效应和时间-效应关系;SCGE和PI单染FCM法,CdTeQDs作用于HL-7702细胞24h后,随着剂量的增加,DNA损伤率逐渐增高,G0/G1期细胞百分率显著下降,S期和G2/M期细胞百分率明显上升(P<0.05);AO/EB检测,CdTe QDs作用后细胞出现凋亡形态学改变;AnnexinⅤ-FITC/PI双荧光标记FCM法,CdTe QDs染毒可促进细胞凋亡,各剂量组细胞凋亡率与对照组比较差异有统计学意义(P<0.05)。结论:CdTe QDs可影响细胞存活,引起DNA损伤、细胞周期阻滞,并诱导细胞凋亡。Objective To investigate the hepatotoxicity and DNA damage induced by thioglycolic acid(TGA)-capped cadmium telluride(CdTe) quantum dots(QDs) in human hepatic cells HL-7702,and to provide experimental evidence for the toxicological research and safety evaluation.Methods The HL-7702 cells were divided into control group and CdTe QDs-treated groups with different concentrations of CdTe QDs(0,6.25,12.50,25.00 and 50.00 mg·L-1,respectively).After treated with CdTe QDs,the cell proliferation was measured by MTT assay,the DNA damage by single cell gel electrophoresis(SCGE),the cell cycle process by propidium iodide(PI)-flow cytometry(FCM) and the apoptosis by acridine orange/ethidium bromide(AO/EB) assay and Annexin Ⅴ-fluorescein isothiocyanate(FITC)/PI-FCM.Results The MTT results showed that CdTe QDs inhibited the proliferation of HL-7702 cells in a dose-dependent and time-dependent manner.The results acquired by SCGE and FCM with PI staining showed that after CdTe QDs exposure for 24 h,as exposure dose increased,the degree of DNA damage raised,and the percentage of HL-7702 cells in G0/G1 phase was decreased while they were significantly increased in S and G2/M phases(P〈0.05).In AO/EB assay,the apoptotic cells were observed under fluorescence microscope;In Annexin Ⅴ-FITC/PI-FCM,the apoptotic rates in CdTe QDs groups were significantly increased compared with control group(P〈0.05).Conclusion CdTe QDs could influence the cell viability,and induce DNA damage,S and G2/M phases arrest and apoptosis in HL-7702 cells.
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