Tang Jian-qiang, Wan Yuan-lian, Liu Yu-cun, Rong Long, Wang Xin, Wu Tao, Pan Yi-sheng, Zhu Jing
Department of General Surgery, Peking University First Hospital, Beijing 100034, China.
Beijing Da Xue Xue Bao Yi Xue Ban. 2007 Oct 18;39(5):453-7.
To assess the expression of Promatrilysin in LoVo colon cancer cell by FVIIa stimulation,and to investigate the effect of MAPKs signal transduction pathway on up-regulation of Promatrilysin.
(1) The expression of ProMMP-7 was detected by Western blot at different time points (0,2,4,6,9,12 and 24 h) and with different doses of (0,0.1,1,5,10,25 and 100 nmol/L) FVIIa stimulation. The change of ProMMP-7 expression was observed with 5 mg/L tissue factor (TF) antibody prior to 100 nmol/L FVIIa. (2) The activation of MAPKs (ERK, p38, JNK) signaling pathways were assessed at different time points after being stimulated with 100 nmol/L FVIIa and the changes of ProMMP-7 expression were detected after the special signal pathway inhibitors (PD98059,SB203580,SP600125) were applied,respectively.
(1) The expression of ProMMP-7 in LoVo cells was up-regulated by FVII a in a time-effect dependent and dose-effect dependent manner,and markedly reached the peak level at h12, 5.5 folds that of the control group (P=0.006).The up-regulation of ProMMP-7 was completely inhibited by blockade with TF antibody. (2) A time-dependent phosphorylation of ERK1/2 and P38 in LoVo cells was induced with FVIIa incubation,reached the peak at min10,2.2 folds and 3.9 folds those of the control groups respectively, but not JNK. (3) The upregulation effect of ProMMP-7 was partially blocked after incubation of ERK1/2 inhibitors PD98059 and P38 inhibitors SB203580 prior to FVIIa, The expression of ProMMP-7 decreased by 32%+/-5% and 61%+/-10% respectively (P<0.05).whereas JNK inhibitors SP600125 did not have the effect.
FVIIa induces tissue factor-dependent up-regulation of ProMMP-7 in LoVo cells. ERK1/2 and p38 signal pathways are not only involved in TF/FVIIa mediated signaling,but also related to the upregulation of MMP-7 in LoVo cells.
通过FVIIa刺激评估基质溶素在LoVo结肠癌细胞中的表达,并研究丝裂原活化蛋白激酶(MAPKs)信号转导通路对基质溶素上调的影响。
(1)采用蛋白质免疫印迹法检测不同时间点(0、2、4、6、9、12和24小时)及不同剂量(0、0.1、1、5、10、25和100 nmol/L)FVIIa刺激下基质金属蛋白酶-7(ProMMP-7)的表达。在100 nmol/L FVIIa刺激前,用5 mg/L组织因子(TF)抗体观察ProMMP-7表达的变化。(2)用100 nmol/L FVIIa刺激后,在不同时间点评估MAPKs(细胞外调节蛋白激酶ERK、p38丝裂原活化蛋白激酶、应激活化蛋白激酶JNK)信号通路的激活情况,并分别应用特异性信号通路抑制剂(PD98059、SB203580、SP600125)后检测ProMMP-7表达的变化。
(1)FVIIa以时间和剂量依赖的方式上调LoVo细胞中ProMMP-7的表达,在12小时时显著达到峰值水平,是对照组的5.5倍(P = 0.006)。TF抗体阻断可完全抑制ProMMP-7的上调。(2)FVIIa孵育诱导LoVo细胞中ERK1/2和P38的时间依赖性磷酸化,分别在10分钟时达到峰值,是对照组的2.2倍和3.9倍,但JNK未出现此现象。(3)在FVIIa刺激前孵育ERK1/2抑制剂PD98059和P38抑制剂SB203580后,ProMMP-7的上调作用部分被阻断,ProMMP-7的表达分别下降了32%±5%和61%±10%(P < 0.05)。而JNK抑制剂SP600125无此作用。
FVIIa诱导LoVo细胞中组织因子依赖性的ProMMP-7上调。ERK1/2和p38信号通路不仅参与TF/FVIIa介导的信号传导,还与LoVo细胞中MMP-7的上调有关。