多效蛋白
天狼星红
四氯化碳
肝小叶
肝星状细胞
病理
免疫组织化学
四氯化碳
血管生成
肝纤维化
生物
纤维化
肝细胞学
化学
癌症研究
内分泌学
生长因子
医学
受体
生物化学
有机化学
肝脏代谢
作者
T Kohashi,Yuko Tateaki,Chise Tateno,Toshimasa Asahara,M Obara,Katsutoshi Yoshizato
标识
DOI:10.1080/08977190290023913
摘要
AbstractPleiotrophin (PTN) is a heparin-binding protein, which induces growth, angiogenesis, differentiation, and transformation of cells. The aim of this study was to examine the role of PTN in liver fibrogenesis. Rats were treated with carbon tetrachloride (CCl 4 ) for 3-9 weeks to induce liver fibrosis. The sirius-red staining of these liver tissue sections clearly showed the development of fibrosis and glutathione S-transferase placental type-positive preneoplastic nodules emerged at 7 weeks of the treatment. PTN expression was investigated in fibrotic liver tissues at the mRNA level using a real-time reverse transcription polymerase chain reaction and at the protein level by immunohistochemistry. Quantity of PTN mRNA increased 5-fold in fibrotic liver tissues at 7 weeks of CCl 4 -treatment over the control values. Immunohistochemistry localized PTN protein on hepatic nonparenchymal cells, mostly stellate cells and some of Kupffer cells, and the preneoplastic nodules in fibrotic liver tissues. PTN mRNA expression is significantly upregulated in the CCl 4 -induced chronic rat fibrotic liver tissues. We suggest that PTN might be involved in fibrogenesis and preneoplastic changes of liver.KeywordsFibrogenesisPleiotrophinPreneoplastic NodulesHepatic Stellate CellsReal-time Reverse Transcription Polymerase Chain ReactionCollagenGlutathione S-transferase Placental Type
科研通智能强力驱动
Strongly Powered by AbleSci AI