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原发性胆汁性肝硬化肝内小胆管中肝细胞生长因子激活剂抑制剂1型(HAI-1)表达增强。

Augmented expression of hepatocytes growth factor activator inhibitor type 1 (HAI-1) in intrahepatic small bile ducts in primary biliary cirrhosis.

作者信息

Sasaki Motoko, Ikeda Hiroko, Kataoka Hiroaki, Nakanuma Yasuni

机构信息

Department of Human Pathology, Kanazawa University Graduate School of Medicine, Kanazawa, 920-8640, Japan.

出版信息

Virchows Arch. 2006 Oct;449(4):462-71. doi: 10.1007/s00428-006-0257-7. Epub 2006 Aug 29.

Abstract

The repair system of damaged biliary mucosa was not fully clarified so far in primary biliary cirrhosis (PBC). Given that related factors of the hepatocyte growth factor (HGF) such as HGF activator (HGFA) and HGFA inhibitor type 1 (HAI-1) participate in the repair of injured gastrointestinal mucosa, we investigated the involvement of the HGF/HGFA/HAI-1 system in PBC and control livers. The expression of HGFA, HAI-1, and c-Met was examined in PBC livers (n=24), diseased livers (control, n=30), and normal livers (n=15) by immunohistochemistry and semiquantitative reverse transcriptase-polymerase chain reaction. We examined the expression of HGFA, HAI-1, and c-Met, and the effect of HGF administration on cell proliferation and wound healing, and HAI expression in cultured mouse biliary epithelial cells (BECs). HAI-1 expression was faint in control livers, whereas it was significantly augmented in damaged small bile ducts, bile ductules, and periportal hepatocytes in PBC (p<0.05). HGFA and c-Met were homogeneously expressed in BECs in PBC and control livers. HAI-1 expression was increased at the front of wound healing and the treatment with HGF-enhanced HAI-1 expression, cell proliferation, and wound healing in cultured BECs. HGF/HGFA/HAI-1 system may participate in biliary mucosal repair as reported in gastrointestinal mucosal repair.

摘要

目前,原发性胆汁性肝硬化(PBC)中受损胆管黏膜的修复系统尚未完全阐明。鉴于肝细胞生长因子(HGF)的相关因子,如HGF激活剂(HGFA)和1型HGFA抑制剂(HAI-1)参与受损胃肠道黏膜的修复,我们研究了HGF/HGFA/HAI-1系统在PBC肝脏和对照肝脏中的作用。通过免疫组织化学和半定量逆转录聚合酶链反应检测了24例PBC肝脏、30例患病肝脏(对照)和15例正常肝脏中HGFA、HAI-1和c-Met的表达。我们检测了HGFA、HAI-1和c-Met的表达,以及HGF给药对细胞增殖和伤口愈合的影响,以及在培养的小鼠胆管上皮细胞(BECs)中HAI的表达。HAI-1在对照肝脏中表达微弱,而在PBC受损的小胆管、胆小管和汇管区肝细胞中显著增强(p<0.05)。HGFA和c-Met在PBC和对照肝脏的BECs中均匀表达。在伤口愈合前沿HAI-1表达增加,HGF处理增强了培养的BECs中HAI-1的表达、细胞增殖和伤口愈合。HGF/HGFA/HAI-1系统可能如胃肠道黏膜修复报道的那样参与胆管黏膜修复。

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