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人前列腺癌细胞系中纤溶酶原激活物活性的多样性与调节

Diversity and modulation of plasminogen activator activity in human prostate carcinoma cell lines.

作者信息

Lyon P B, See W A, Xu Y, Cohen M B

机构信息

Department of Urology, University of Iowa, Iowa City 52242-1089, USA.

出版信息

Prostate. 1995 Oct;27(4):179-86. doi: 10.1002/pros.2990270402.

Abstract

Baseline cellular plasminogen activator (PA) activity, and the cellular proteins responsible for variations in PA activity were evaluated in three human prostate carcinoma cell lines. Net PA activity in the cell lines PC-3, DU-145, and LNCaP was measured using a plasminogen-dependent fibrin lysis assay. These three cell lines were then analyzed to determine the specific protein(s) responsible for differences in PA activity. mRNA and protein levels of cellular urinary PA (uPA), tissue PA (tPA), PA inhibitor 1 (PAI1), PA inhibitor 2 (PAI2), and uPA receptor (uPAr) were measured using Northern analysis and ELISA assays. Net cellular PA activity in the three cell lines varied over a 3-fold range (PC3 > DU145 >> LNCaP). Net PA activity in the fibrinolysis assay demonstrated a direct correlation with mRNA transcript levels of uPA, tPA, PAI1, and uPAr (PC-3 > DU-145 > LNCaP). uPA protein was identified in both the PC-3 and the DU-145 lines. tPA, PAI1, and PAI2 proteins were identified only in PC-3 cells. In general, cellular protein levels correlated with mRNA levels. These findings demonstrate that prostate carcinoma cell lines vary in their net PA activity. This variability results from both qualitative and quantitative differences in the cellular expression of PA regulatory proteins.

摘要

在三种人前列腺癌细胞系中评估了基线细胞纤溶酶原激活剂(PA)活性以及负责PA活性变化的细胞蛋白。使用纤溶酶原依赖性纤维蛋白溶解测定法测量了PC-3、DU-145和LNCaP细胞系中的净PA活性。然后分析这三种细胞系,以确定导致PA活性差异的特定蛋白质。使用Northern分析和ELISA测定法测量细胞尿激酶型PA(uPA)、组织型PA(tPA)、PA抑制剂1(PAI1)、PA抑制剂2(PAI2)和uPA受体(uPAr)的mRNA和蛋白质水平。三种细胞系中的净细胞PA活性在3倍范围内变化(PC3>DU145>>LNCaP)。纤维蛋白溶解测定中的净PA活性与uPA、tPA、PAI1和uPAr的mRNA转录水平直接相关(PC-3>DU-145>LNCaP)。在PC-3和DU-145细胞系中均鉴定出uPA蛋白。仅在PC-3细胞中鉴定出tPA、PAI1和PAI2蛋白。一般来说,细胞蛋白水平与mRNA水平相关。这些发现表明,前列腺癌细胞系的净PA活性各不相同。这种变异性是由PA调节蛋白细胞表达的定性和定量差异导致的。

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