• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

[四氯化碳诱导肝纤维化急性和慢性期的病理形态学:免疫组织化学和原位杂交研究]

[Pathomorphology of acute and chronic stages of CCl4-induced liver fibrosis: immunohistochemical and in situ hybridization studies].

作者信息

Herbst H, Milani S, Heinrichs O, Schuppan D

机构信息

Institut für Pathologie, Klinikum Steglitz, Freie Universität Berlin, BRD.

出版信息

Z Gastroenterol. 1992 Mar;30 Suppl 1:21-8.

PMID:1449012
Abstract

The cellular localization of expression of various genes activated during the course of liver fibrosis and regeneration was studied by immunohistology and in situ hybridization in rat and human liver tissues. Mesenchymal cells proved to be the principal sources of extracellular matrix proteins and of fibrogenic growth factors, whereas the collagenase-activating protease transin/stromelysin gene was transcribed in parenchymal cells as well. Fibrogenesis by the mesenchymal compartment appears to be balanced by fibrolysis controlled by parenchymal cell functions. Continuous parenchymal damage may thus disrupt this balance between fibrogenesis and fibrolysis, resulting in fibrosis.

摘要

通过免疫组织学和原位杂交技术,对大鼠和人类肝脏组织中肝纤维化和再生过程中激活的各种基因的表达细胞定位进行了研究。间充质细胞被证明是细胞外基质蛋白和促纤维化生长因子的主要来源,而胶原酶激活蛋白酶转胶酶/基质溶解素基因也在实质细胞中被转录。间充质部分的纤维化似乎由实质细胞功能控制的纤维溶解所平衡。因此持续的实质损伤可能会破坏纤维化和纤维溶解之间的这种平衡,导致纤维化。

相似文献

1
[Pathomorphology of acute and chronic stages of CCl4-induced liver fibrosis: immunohistochemical and in situ hybridization studies].[四氯化碳诱导肝纤维化急性和慢性期的病理形态学:免疫组织化学和原位杂交研究]
Z Gastroenterol. 1992 Mar;30 Suppl 1:21-8.
2
[Fibrogenesis and fibrolysis in the liver].[肝脏中的纤维生成与纤维溶解]
Verh Dtsch Ges Pathol. 1995;79:15-27.
3
Cellular distribution of transforming growth factor-beta 1 and procollagen types I, III, and IV transcripts in carbon tetrachloride-induced rat liver fibrosis.四氯化碳诱导的大鼠肝纤维化中转化生长因子-β1及I、III、IV型前胶原转录本的细胞分布
J Clin Invest. 1990 Jun;85(6):1833-43. doi: 10.1172/JCI114643.
4
Transforming growth factor-beta 1 and type I procollagen transcripts during regeneration and early fibrosis of rat liver.大鼠肝脏再生和早期纤维化过程中转化生长因子-β1及I型前胶原转录本
Lab Invest. 1990 Aug;63(2):171-80.
5
Spatial and temporal patterns of gene expression for the proteoglycans biglycan and decorin and for transforming growth factor-beta 1 revealed by in situ hybridization during experimentally induced liver fibrosis in the rat.大鼠实验性肝纤维化过程中,通过原位杂交揭示的核心蛋白聚糖双糖链蛋白聚糖和饰胶蛋白聚糖以及转化生长因子-β1基因表达的时空模式。
Hepatology. 1993 Sep;18(3):581-9.
6
Transforming growth factor beta gene expression is transiently enhanced at a critical stage during liver regeneration after CCl4 treatment.在四氯化碳处理后的肝脏再生关键阶段,转化生长因子β基因表达会短暂增强。
Lab Invest. 1993 Sep;69(3):283-94.
7
Tissue inhibitor of metalloproteinase-1 and -2 RNA expression in rat and human liver fibrosis.金属蛋白酶组织抑制剂-1和-2在大鼠及人类肝纤维化中的RNA表达
Am J Pathol. 1997 May;150(5):1647-59.
8
Low molecular weight heparin prevents hepatic fibrogenesis caused by carbon tetrachloride in the rat.低分子量肝素可预防四氯化碳所致大鼠肝纤维化。
J Hepatol. 2007 Feb;46(2):286-94. doi: 10.1016/j.jhep.2006.08.023. Epub 2006 Oct 25.
9
[Dynamic expression of tenascin in rat liver during liver fibrogenesis induced by CCl(4)].
Zhonghua Gan Zang Bing Za Zhi. 2002 Feb;10(1):40-2.
10
Hepatic fibrogenesis: the puzzle of interacting cells, fibrogenic cytokines, regulatory loops, and extracellular matrix molecules.肝纤维化形成:相互作用的细胞、纤维化细胞因子、调节环路及细胞外基质分子之谜
Z Gastroenterol. 1992 Mar;30 Suppl 1:5-16.