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丝裂原活化蛋白激酶(MAPK)级联途径和P53途径对肝移植的影响。

Impact of MAPK cascade pathway and P53 pathway upon liver transplant.

作者信息

Gong Nianqiao, Li Guoxun, Xiao Jiansheng, Guo Hui, Ye Qifa

机构信息

Institute of Organ Transplantation, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.

出版信息

J Huazhong Univ Sci Technolog Med Sci. 2005;25(5):555-7. doi: 10.1007/BF02896016.

DOI:10.1007/BF02896016
PMID:16463673
Abstract

The change and the role of MAPK cascade pathway and P53 pathway after liver transplantation were explored. Thirty-four punctured donor liver specimens and 10 normal liver specimens were classified as group A (no rejection, n = 10), group B (mild/moderate acute rejection, n = 10), group C (serious acute rejection, n = 8), group D (chronic rejection/fibrosis, n = 6) and group E (control, n = 10). By using immunohistochemistry, the expression levels of mitogen activated protein kinase (MAPK), Ras and P53 proteins, and by in situ hybridization, MAPK and ras mRNA expression levels were detected. The results showed that the expression levels of MAPK and Ras proteins were increased by turns in groups A, B and C, and decreased by turns in groups D and E. The protein expression of P53 was higher in the treated groups. The expression of Ras, HSP70 mRNA was identical as that of protein. It is suggested that the MAPK cascade pathway and P53 pathway can protect the hepatocytes by different mechanisms after liver transplantation. MAPKs cascade pathway repairs hepatocyte injury or accelerates hepatocytes into proliferation or differentiation. P53 pathway blocks cell cycle within G1 phase to make hepatocyte repair or apoptosis to reduce disorder differentiation.

摘要

探讨肝移植后丝裂原活化蛋白激酶(MAPK)级联通路和P53通路的变化及作用。将34例穿刺获取的供肝标本和10例正常肝标本分为A组(无排斥反应,n = 10)、B组(轻度/中度急性排斥反应,n = 10)、C组(重度急性排斥反应,n = 8)、D组(慢性排斥反应/纤维化,n = 6)和E组(对照组,n = 10)。采用免疫组织化学法检测丝裂原活化蛋白激酶(MAPK)、Ras和P53蛋白的表达水平,采用原位杂交法检测MAPK和ras mRNA表达水平。结果显示,MAPK和Ras蛋白表达水平在A、B、C组依次升高,在D、E组依次降低。P53蛋白在各处理组表达较高。Ras、HSP70 mRNA的表达与蛋白表达一致。提示肝移植后MAPK级联通路和P53通路可通过不同机制保护肝细胞。MAPK级联通路修复肝细胞损伤或加速肝细胞增殖或分化。P53通路在G1期阻断细胞周期,使肝细胞修复或凋亡以减少分化紊乱。

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Impact of MAPK cascade pathway and P53 pathway upon liver transplant.丝裂原活化蛋白激酶(MAPK)级联途径和P53途径对肝移植的影响。
J Huazhong Univ Sci Technolog Med Sci. 2005;25(5):555-7. doi: 10.1007/BF02896016.
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本文引用的文献

1
Ki67, E-cadherin, and p53 as prognostic indicators of long-term outcome after liver transplantation for metastatic neuroendocrine tumors.Ki67、E-钙黏蛋白和p53作为转移性神经内分泌肿瘤肝移植术后长期预后的指标
Transplantation. 2002 Feb 15;73(3):386-94. doi: 10.1097/00007890-200202150-00012.
2
Effects of a p38 mitogen-activated protein kinase inhibitor as an additive to university of wisconsin solution on reperfusion injury in liver transplantation.p38丝裂原活化蛋白激酶抑制剂作为威斯康星大学保存液添加剂对肝移植再灌注损伤的影响
Transplantation. 2001 Jul 15;72(1):22-7. doi: 10.1097/00007890-200107150-00007.
3
JNK and p38MAPK are activated during graft reperfusion and not during cold storage in rat liver transplantation.
Transplant Proc. 2001 Feb-Mar;33(1-2):931-2. doi: 10.1016/s0041-1345(00)02273-9.
4
Intragraft expression of p38 in rat small bowel transplantation.p38在大鼠小肠移植中的移植物内表达
Transplant Proc. 2000 Sep;32(6):1281-2. doi: 10.1016/s0041-1345(00)01226-4.
5
Role of p21Waf1/Cip1/Sdi1 in cell death and DNA repair as studied using a tetracycline-inducible system in p53-deficient cells.利用四环素诱导系统在p53缺陷细胞中研究p21Waf1/Cip1/Sdi1在细胞死亡和DNA修复中的作用。
Oncogene. 1997 Apr 17;14(15):1875-82. doi: 10.1038/sj.onc.1201004.
6
Opposing effects of ERK and JNK-p38 MAP kinases on apoptosis.细胞外信号调节激酶(ERK)与应激活化蛋白激酶(JNK)-p38丝裂原活化蛋白激酶(MAPK)对细胞凋亡的相反作用。
Science. 1995 Nov 24;270(5240):1326-31. doi: 10.1126/science.270.5240.1326.