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:张启良[1] 陈岚[1] 刘玮[1] 张健[1] 杨君蕊[1] 张建平[1]
机构地区:[1]上海第二医科大学病理生理学教研室
出 处:《上海第二医科大学学报》2000年第2期102-104,178,共4页Acta Universitatis Medicinalis Secondae Shanghai
基 金:国家自然科学基金!(39670327);上海市科技发展基金!(97ZB14018);胡应洲基金
摘 要:目的测定和比较不同正常细胞及人类肿瘤细胞膜上尿型纤溶酶原活化素受体(uPAR)的表达,了解肿瘤细胞表达uPAR的基本性质。方法建立并应用受体放射配基结合分析法(receptor- radio- ligand binding assay, RBA)测定细胞膜上的uPAR。结果 成纤维细胞经不同处理,U937细胞以PMA处理不同时间,测定uPAR的结果无论表达量或平衡解离常数(Kd)的变化均与文献一致。对正常细胞和肿瘤细胞株共10种测定膜上uPAR,结果肺癌、肝癌等5种人类肿瘤细胞比人成纤维细胞、牛内皮细胞等正常组织细胞的表达数明显多。结论 本研究进一步证明了uPAR表达增强是多种恶性肿瘤细胞的一种特点。Objective This study was designed to quantitatively determine and compare the expression of urokinase -- type plasminogen activator receptor (uPAR) in different normal cells and/with different cultured tumor cell lines. Methods The method of radioligand binding assay of receptor (RBA) for examination of uPAR on the cell membrane has been established with 125I -- DFP -- uPA, a radioligand agent prepared in our laboratory, and used to monitor the uPAR levels in all experiments. Results The number of uPAR expressed and the affinity for uPAR to combine with its specific lgand, uPA, were examined using RBA method in ten buds of cells, including five kinds of normal cells and five cultured tumor cell lines, such as myeloid leukemic cell lines of U937 and HL-- 60, lung cancer cell line A410, hepatic cancer cell line Bel 7402 and gastric carcinoma cell line N -- 45. The uPAR expression was not found in human red blood cells, and the uPAR expression of all examined malignant tumor cell lines was much stronger than that of the normal tissue cells. Conclusion it is further confirmed that high uPAR expression is characteristic for most of the malignant tumors' cells. The method can be used to study the role of uPAR and the influence factors for uPAR expression in laboratory experiments.
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:216.73.216.171