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:杨晓姗[1] 林雅军[2] 魏洁[2] 胡刚[2] 徐蓉[1] 许晓东[3] 马桂蕾[1] 孙洪范[1]
机构地区:[1]北京协和医学院中国医学科学院生物医学工程研究所,天津市生物医学材料重点实验室,天津300192 [2]卫生部北京医院:卫生部北京老年医学研究所,卫生部老年医学重点实验室,北京100730 [3]卫生部北京医院血液科,北京100730
出 处:《第三军医大学学报》2014年第19期1991-1995,共5页Journal of Third Military Medical University
基 金:国家自然科学基金(81001439)~~
摘 要:目的探讨重组人p66Shc腺病毒(AdenoⅩ-p66Shc)对宫颈癌HeLa细胞增殖的抑制作用及机制。方法MTT法检测细胞活力,DCFH-DA荧光探针检测活性氧(ROS)生成;ELISA检测8-羟基脱氧鸟苷(8-OHdG)含量;AnnexinⅤ-FITC/PI荧光染色检测细胞凋亡率;Western blot检测相关蛋白表达;免疫共沉淀检测p66Shc与p53之间相互作用。结果重组人p66Shc腺病毒呈剂量依赖性地抑制HeLa细胞增殖(P<0.05),而N-乙酰半胱氨酸能够阻断重组人p66Shc腺病毒的作用。p66Shc能引起细胞ROS水平显著上升(P<0.05),同时伴随8-OHdG含量的升高(P<0.05);p66Shc能引起p53蛋白和CyclinB1蛋白表达及p53磷酸化修饰(p-p53)显著升高(P<0.05),但免疫共沉淀实验结果显示p66Shc与p53并非直接结合,提示p66Shc通过其他信号分子间接调控p53的表达及活性。结论重组人p66Shc腺病毒通过使HeLa细胞ROS水平上升,引起DNA氧化损伤,从而诱导p53表达及其磷酸化修饰升高抑制HeLa细胞增殖。Objective To determine the inhibitory effect of a recombinant adenovirus of human p66Shc (Adeno X-p66She ) on the proliferation of human eervieal eaneer HeLa cells and investigate the possible underlying mechanism. Methods The Hela cells were infected with Adeno X-LacZ and Adeno X-p66She respectively. The eells without infeetion served as blank control. Cell viability was analyzed by MTT assay. Reactive oxygen species (ROS) was measured by DCFH-DA fluorescent probes and flow cytometry. The levels of 8-OHdG were detected by ELISA assay. Cell apoptosis was detected by Annexin V-FITC/PI staining. Western blotting was used to observe the expression of associated proteins. Co-immunopreeipitation (Co-IP) was used to investigate the possible interaction between p66She and p53. Results MTT assay showed that the proliferation of HeLa cells was significantly suppressed ( P 〈 0.05 ) by Adeno X-p66She in a dose-dependent manner, and its inhibition eould be blocked by N-aeetyl-L-eysteine. Meanwhile, the levels of ROS and 8-OHdG were significantly increased after Adeno X-p66Shc infection ( P 〈 0.05 ). The expression of p53, Cyelin B1 and p-p53 was up-regulated with the over-expression of p66She, but the result of Co-IP demonstrated that p66Shc and p53 were not direetly eombined, suggesting the expression and activity of p53 was regulated by other molecular aetivated by p66She. Conclusion Adeno X-p66She induces ROS generation and DNA oxidative damage, and up-regulates the expression of p53 and p-p53, and thereby inhibits the proliferation of HeLa eells.
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:18.116.165.143