Cheng Chun-ying, Sun Yong, Wen Zhi-bin, He Xiao-fan, Wang Gu-feng, Lin Guo-qiang, Jiang Hai-he, Tian Xian-ming, He Shi-lin
Xiangya Medical School, Central South University, Changsha 410078, China.
Nan Fang Yi Ke Da Xue Xue Bao. 2009 Aug;29(8):1743-7.
To observe the effects of tetramethylpyrazine (TMP) on tissue factor (TF) expression induced by thrombin in human umbilical vein endothelium derived cell line ECV304.
The changes in the total cellular procoagulant activity (PCA) of ECV304 cells exposed to thrombin were observed with one-stage clotting assay. TF mRNA expression in the exposed cells was examined using semi-quantitative reverse transcription-polymerase chain reaction (RT-PCR).
ECV304 cells stimulated with increasing concentrations of thrombin (1.25-20 U/ml) showed a gradual increase of PCA (r=0.9602, P<0.01). The application of FVII-deficient plasma and the monoclonal antibody of TF confirmed that the PCA of the cells mediated by TF activity. TMP at 125-1000 microg/ml alone did not affect TF expression in ECV304 cells (P>0.20), TMP administered 30 min prior to thrombin exposure showed a significant concentration-dependent inhibitory effect on the increments of PCA (r=-0.9644, P<0.01) and TF mRNA expression (r=-0.9576, P<0.05) in ECV304 cells, and 1000 microg/ml TMP produced the strongest effect. In ECV304 cells stimulated with thrombin for 4, 6, 8, 10 and 12 h, TMP administration significantly inhibited the thrombin-induced PCA, and the effect was especially obvious at 8 h following thrombin exposure (P<0.05).
Thrombin induces TF expression in vascular endothelial cells, and this effect can be inhibited by TMP at the mRNA level.
观察川芎嗪(TMP)对凝血酶诱导人脐静脉内皮细胞系ECV304组织因子(TF)表达的影响。
采用一期凝固法观察凝血酶作用下ECV304细胞总细胞促凝活性(PCA)的变化。用半定量逆转录聚合酶链反应(RT-PCR)检测受刺激细胞中TF mRNA的表达。
用不同浓度(1.25 - 20 U/ml)凝血酶刺激ECV304细胞,PCA呈逐渐升高趋势(r = 0.9602,P < 0.01)。应用缺乏FVII的血浆和TF单克隆抗体证实细胞的PCA由TF活性介导。单独使用125 - 1000 μg/ml的TMP对ECV304细胞TF表达无影响(P > 0.20),在凝血酶暴露前30分钟给予TMP对ECV304细胞PCA的升高(r = -0.9644,P < 0.01)和TF mRNA表达(r = -0.9576,P < 0.05)有显著的浓度依赖性抑制作用,1000 μg/ml TMP作用最强。在凝血酶刺激4、6、8、10和12小时的ECV304细胞中,给予TMP可显著抑制凝血酶诱导的PCA,在凝血酶暴露后8小时作用尤为明显(P < 0.05)。
凝血酶可诱导血管内皮细胞表达TF,TMP在mRNA水平可抑制这一作用。