摘要
目的:研究尿激酶型纤溶酶原(u P A) 激活系统中4 种主要成分u P A、 P A I1 、 P A I2 、u P A R 在非小细胞性肺癌细胞株中的表达及各因子之间的作用方式。方法:应用免疫组化、蛋白免疫印迹技术对培养细胞中4 种成分进行定位、定性及半定量分析;应用斑点杂交技术检测4 种细胞中u P A m R N A 和u P A Rm R N A 的表达。结果:4 种成分在4 株细胞的胞浆及胞膜均有表达。蛋白免疫印迹法检测u P A、 P A I1 、 P A I2 、u P A R,4 株细胞均在约140 ku 和约80 ku 处出现特异性条带,且两种腺癌细胞的表达水平显著高于其他两株细胞。斑点杂交结果示4 株细胞中均有u P A m R N A 和u P A R m R N A 的表达。结论:此4 株细胞中均能合成与分泌u P A 系统的4 种主要成分,各因子以二联及三联复合物(u P A/ P A I1 、u P A/ P A I2 、u P A/u P A R、u P A/ P A I1/u P A R、u P A/ P A I2/u P A R) 的形式存在;u P A 系统的表达与这4 种细胞的恶性程度并不一致。
Objective : To study the expression and the reaction patterns ofthe main components ofthe u P Asystem(u P A, P A I 1 , P A I 2 ,u P A R)in non small celllung cancer celllines . Methods :u P Asystem was detected and analyzedusing immunohistochemistry and Western Blot. Dot blot hybridization was used to detect the expression of u P A, u P A Rm R N A. Results : The four components of u P Asystem were expressed in the plasma and membrane ofthe four celllines . Using Western blotto detectthe expression of u P A, P A I 1 , P A I 2 ,u P A R,specific appeared special bands near 80 ku and140 ku were observed , and the expression level of the two adenocarcinoma cell lines was significantly higher than theother two cell lines. Both u P Aand u P A R m R N A were expressed by the four celllines . Conclusions : The four compo nents of u P Asystem could be synthesized and secreted by allthe four celllines ,existed in duplet ortriplet form (u P A/ P A I 1 ,u P A/ P A I 2 ,u P A/u P A R,u P A/ P A I 1/u P A Rand u P A/ P A I 2/u P A R) . The expression of u P Asystem were notinconcomitance with the malignance ofthe celllines .
出处
《中山医科大学学报》
CSCD
1999年第3期174-177,共4页
Academic Journal of Sun Yat-sen University of Medical Sciences
基金
国家自然科学基金
关键词
肺癌
非小细胞肺癌
尿激酶
细胞培养
Subject headings urokinase
carcinoma ,non small cell lung
cells,cultured