检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:巩凡[1] 张帮勇 黄艳梅[1] 张婷[1] 薛玉英[1] 唐萌[1]
机构地区:[1]东南大学公共卫生学院环境医学工程教育部重点实验室江苏省生物材料与器件重点实验室,江苏南京210009
出 处:《环境与健康杂志》2014年第10期893-896,共4页Journal of Environment and Health
基 金:国家重大科学研究计划项目(2011CB933404);国家自然科学基金(81172697;81473003);江苏省自然科学基金(BK2011606)
摘 要:目的探讨纳米银在人肝癌(Hep G2)细胞株及人正常肝(L02)细胞株内的生物分布及引起凋亡作用差异的可能机制。方法将HepG2细胞、L02细胞分别暴露于终浓度为0(对照)、20、40、80、160μg/ml含纳米银的细胞培养液中24、48 h。采用透射电镜(TEM)观察细胞超微结构及颗粒分布;采用流式细胞术检测细胞线粒体膜电位下降细胞比例和活性氧(ROS)水平的变化。结果染毒24 h时,HepG2和L02细胞的细胞膜受损,在膜周围可见黑色颗粒;染毒48 h时,在HepG2细胞的线粒体及L02细胞的溶酶体和内吞小泡中发现黑色颗粒。与对照组相比,20-160μg/ml纳米银暴露Hep G2细胞24、48 h以及40、80、160μg/ml纳米银暴露L02细胞24 h及80、160μg/ml纳米银暴露L02细胞48 h时的线粒体膜电位下降细胞比例均较高,差异有统计学意义(P〈0.05,P〈0.01);且随着纳米银暴露浓度的升高暴露时间的延长,HepG2细胞和L02细胞的线粒体膜电位下降细胞比例均呈上升趋势。与对照组相比,20-160μg/ml纳米银暴露HepG2细胞24、48 h的ROS水平上升明显,差异有统计学意义(P〈0.01);且随着纳米银暴露浓度的升高暴露时间的延长,HepG2细胞ROS水平呈上升趋势;各剂量纳米银暴露L02细胞中ROS水平无明显变化。结论纳米银在HepG2和L02细胞中的生物分布不同对这两种细胞的凋亡造成了不同的影响。Objective To investigate the bio-distribution of silver nanoparticles in human hepatoma cell line(HepG2) cells and human normal liver cell line(L02) cells in vitro and the possible mechanism of apoptosis induced by silver nanoparticles.Methods The HepG2 cells and the L02 cells were used. The two cell lines were treated with silver nanoparticles at the level of 20-160 μg/ml for 24 h and 48 h in vitro. The cell morphology and particle distribution in cells were observed by transmission electron microscopy(TEM). The changes of mitochondrial membrane potential and the production of reactive oxygen species(ROS) were determined by flow cytometry assay. Results After 24 h of treatment,impaired cell membranes and black particles around the membrane were found in both HepG2 cells and L02 cells. After 48 h of treatment,black particles could be detected in the mitochondria of HepG2 cells,while in the lysosome and endocytic vesicle of L02 cells. Compared with the control group,HepgG2 cells treated with 20-160 μg/ml silver nanoparticles for 24 h and 48 h groups,L02 cells treated with40,80,160 μg/ml silver nanoparticles for 24 h groups and 80,160 μg/ml silver nanoparticles for 48 h groups showed a higher ratio of the cells whose mitochondrial membrane potential reducing(P〈0.05,P〈0.01). With the increased exposure concentration and the extended exposure time,the ratio showed an upward trend. Compared with the control group,HepgG2 cells treated with20-160 μg/ml silver nanoparticles for 24 h and 48 h groups showed a higher ROS level(P〈0.05,P〈0.01). With the increased exposure concentration and the extended exposure time,the ROS level showed an upward trend. Conclusion The different bio-distribution of silver nanoparticles may cause the different effects of apoptosis in HepG2 cells and L02 cells.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.229