期刊文献+

RhoA和肌球蛋白轻链在肝纤维化大鼠肝组织中的表达 被引量:6

Expressions of RhoA and phosphorylated myosin light chain in rat liver tissue undergoing hepatic fibrogenesis
暂未订购
导出
摘要 目的观察Rho/Rho激酶信号转导通路关键信号分子RhoA和磷酸化肌球蛋白轻链[p-MLC(Thr18/Ser19)]在大鼠肝纤维化组织中的表达规律。方法HE及Masson三色染色观察肝病理组织学变化;用Western blot检测RhoA、p-MLC(Thr18/Ser19)蛋白的表达;RT-PCR方法检测RhoAmRNA的表达。结果随着肝纤维化的进展,RhoA、p-MLC(Thr18/Ser19)蛋白表达明显增加,RhoAmRNA基因表达也逐渐加强。RhoA和p-MLC(Thr18/Ser19)分别与α-平滑肌肌动蛋白(α-SMA)呈显著正相关。结论Rho/Rho激酶信号转导通路在肝纤维化形成过程中发生变化。 Objective To observe the expressive changes of RhoA and phosphorylated myosin light chain in rat liver tissue undergoing hepatic fibrogenesis. Methods The liver histopathological changes were evaluated by hematoxylin and eosin staining and Masson' s trichrome method. Western blot was used to determine the expressions of RhoA and p-MLC(Thr18/Ser19), and reverse transcription-polymerase chain reaction (RT-PCR) to determine the expression of RhoA mRNA. Results With the development of hepatic fibrogenesis, the protein expressions of RhoA and p-MLC (Thr18/Ser19) and the mRNA expression of RhoA were significantly increased. RhoA and p-MLC (Thr18/Ser19) correlated with α-SMA positively, respectively. Conclusion Rho/ROCK signaling pathways are nesis.
出处 《基础医学与临床》 CSCD 北大核心 2007年第3期275-278,共4页 Basic and Clinical Medicine
基金 河北省科学技术厅资助项目(06276102D-117)
关键词 RHOA p-MLC(Thr18/Ser19) 肝纤维化 信号通路 RhoA p-MLC ( Thr18/Ser19) hepatic fibrosis signaling pathway
  • 相关文献

参考文献9

二级参考文献47

  • 1Taylor JM, Mack CP, Nolan K, et al. Selective expression of an endogenous inhibitor of FAK regulates proliferation and migration of vascular smooth muscle cells[J]. Mol Cell Biol,2001,21(5):1565-1572.
  • 2Almeida EA, Ilic D, Han Q, et al. Matrix survival signaling: from fibronectin via focal adhesion kinase to c-Jun NH(2)-terminal kinase[J]. J Cell Biol,2000,149(3):741-754.
  • 3Benyon RC,Arthur MJ. Extracellular matrix degradation and the role of hepatic stellate cells[J]. Semin Liver Dis,2001,21(3):373-384.
  • 4Cassiman D,Libbrecht L,Desmet V,et al. T. Hepatic stellate cell/myofibroblast subpopulations in fibrotic human and rat livers[J]. J Hepatol,2002,36:200-209.
  • 5Ramm GA,Carr SC,Bridle KR,et al. Morphology of liver repair following cholestatic liver injury:resolution of ductal hyperplasia,matrix deposition and regression of myofibroblasts[J]. Liver,2000,20:387-396.
  • 6Guan JL. Role of focal adhesion kinase in integrin signaling[J]. Int J Biochem Cell Biol,1997,29 (8-9):1085-1096.
  • 7Schaller MD. Biochemical signals and biological responses elicited by the focal adhesion kinase[J]. Biochim Biophys Acta,2001,1540(1):1-21.
  • 8Hungerford JE,Compton MT,Matter ML,et al. Inhibition of pp125FAK in cultured fibroblasts results in apoptosis[J]. J Cell Biol 1996,135(5):1383-1390.
  • 9Boudreau NJ, Jones PL.Extracellular matrix and integrin signalling: the shape of things to come[J]. Biochem J,1999,339 ( Pt 3):481-488.
  • 10Carloni V,Pinzani M,Giusti S,et al. Tyrosine phosphorylation of focal adhesion kinase by PDGF is dependent on ras in human hepatic stellate cells[J]. Hepatology,2000,31(1):131-140.

共引文献48

同被引文献45

引证文献6

二级引证文献20

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部