Li Guo-xun, Gong Nian-qiao, Ye Qi-fa, Guo Hui
Institut of Organ transplantation, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
Zhonghua Gan Zang Bing Za Zhi. 2003 Dec;11(12):742-4.
To explorer the change of several signal pathway and their signal after liver transplantation.
Classified 34 punctured donor liver samples and 10 normal liver samples as A (no rejection) groups, B (mild/moderate acute rejection) groups, C (serious acute rejection) groups, D (chronic rejection/fibrosis) groups and E (control) groups, MAPK, Ras and p53 were performed immunohistochemistry analysis and image analysis. MAPK and Ras were performed in situ hybridizition. Then image analysis was performed.
The protein expression of MAPK, Ras, increase by turns of A, B and C groups (1.42+/-0.28, 3.88+/-0.87, 6.68+/-0.57 in MAPK; 1.27+/-0.12, 2.80+/-0.30, 3.93+/-0.20 in Ras; corresponding), and decrease by turns of D and E groups (1.49+/-0.37, 0.88+/-0.20 in MAPK; 1.47+/-0.21, 1.01+/-0.12 in Ras; corresponding, F=178.39 in MAPK and 320.59 in Ras, groups B, C vs groups A, D, E, P<0.001 in MAPK and Ras), The protein expression of p53 is higher in treated groups (The results of groups A to E are 2.09+/-0.13, 2.39+/-0.11, 2.03+/-0.19, 2.26+/-0.18 and 0.35+/-0.08, corresponding, F=360.08, groups E vs groups A, B, C, D, P<0.001). Expression of MAPK, Ras mRNA is as same as that of protein.
The MAPKs pathway has role in rejection response after liver transplantation. And it seemed that the MAPKs and p53 are one regulation mechanism for protecting the hepatocyte from damage after liver transplantation.
探讨肝移植后几种信号通路及其信号的变化。
将34份穿刺获取的供肝样本和10份正常肝样本分为A(无排斥反应)组、B(轻度/中度急性排斥反应)组、C(重度急性排斥反应)组、D(慢性排斥反应/纤维化)组和E(对照)组,对丝裂原活化蛋白激酶(MAPK)、Ras和p53进行免疫组织化学分析及图像分析。对MAPK和Ras进行原位杂交,然后进行图像分析。
MAPK、Ras的蛋白表达随A、B、C组依次升高(MAPK分别为1.42±0.28、3.88±0.87、6.68±0.57;Ras分别为1.27±0.12、2.80±0.30、3.93±0.20),随D、E组依次降低(MAPK分别为1.49±0.37、0.88±0.20;Ras分别为1.47±0.21、1.01±0.12,MAPK中F=178.39,Ras中F=320.59,B、C组与A、D、E组比较,MAPK和Ras中P<0.001),p53的蛋白表达在各处理组中较高(A至E组结果分别为2.09±0.13、2.39±0.11、2.03±0.19、2.26±0.18和0.35±0.08,F=360.08,E组与A、B、C、D组比较,P<0.001)。MAPK、Ras mRNA的表达与蛋白表达情况相同。
MAPKs通路在肝移植后的排斥反应中起作用。似乎MAPKs和p53是肝移植后保护肝细胞免受损伤的一种调节机制。