Lamireau Thierry, Dubuisson Liliane, Lepreux Sébastien, Bioulac-Sage Paulette, Fabre Monique, Rosenbaum Jean, Desmoulière Alexis
Groupe de Recherches pour l'Etude du Foie, Université Victor Segalen, Bordeaux, France.
Am J Surg Pathol. 2002 May;26(5):637-46. doi: 10.1097/00000478-200205000-00010.
Fibrillin-1, one of the main constituents of microfibrils, is present in normal adult liver and overexpressed in fibrotic area around cirrhotic nodules and hepatocellular carcinoma. In this work fibrillin-1 expression was studied by immunohistochemistry in liver samples from children with various cholestatic diseases corresponding to paucity of intrahepatic bile ducts, biliary atresia, congenital hepatic fibrosis, Byler's disease, mitochondrial cytopathy, sclerosing cholangitis, or choledochal cyst. As controls, histologically normal liver samples were used. In control liver, as in adult, fibrillin-1 was expressed in vessel walls, sinusoids, and portal connective tissue, particularly at the interface with the limiting hepatocytic plate and close to the basement membrane of bile ducts. In paucity of intrahepatic bile ducts without fibrosis, the fibrillin-1 distribution was similar to controls. In cholestatic diseases associated with severe fibrosis, such as biliary atresia, congenital hepatic fibrosis, Byler's disease, mitochondrial cytopathy, or sclerosing cholangitis, an enhanced deposition of fibrillin-1 was observed in portal connective tissue and fibrous septa. The strong fibrillin-1 expression close to the basement membrane of biliary structures was lost in cholestatic diseases, except biliary atresia. Finally, in normal and pathologic tissues, fibrillin-1 was co-localized with its putative receptor alphaVbeta3 in sinusoids but not around biliary structures.
原纤维蛋白-1是微原纤维的主要成分之一,存在于正常成人肝脏中,并在肝硬化结节和肝细胞癌周围的纤维化区域中过度表达。在这项研究中,通过免疫组织化学方法对患有各种胆汁淤积性疾病的儿童肝脏样本中的原纤维蛋白-1表达进行了研究,这些疾病包括肝内胆管稀少、胆道闭锁、先天性肝纤维化、比勒氏病、线粒体细胞病、硬化性胆管炎或胆总管囊肿。作为对照,使用了组织学上正常的肝脏样本。在对照肝脏中,与成人肝脏一样,原纤维蛋白-1在血管壁、肝血窦和门管区结缔组织中表达,特别是在与肝界板的交界处以及靠近胆管基底膜的位置。在没有纤维化的肝内胆管稀少病例中,原纤维蛋白-1的分布与对照相似。在与严重纤维化相关的胆汁淤积性疾病中,如胆道闭锁、先天性肝纤维化、比勒氏病、线粒体细胞病或硬化性胆管炎,在门管区结缔组织和纤维间隔中观察到原纤维蛋白-1沉积增加。除胆道闭锁外,在胆汁淤积性疾病中,靠近胆管结构基底膜的强烈原纤维蛋白-1表达消失。最后,在正常和病理组织中,原纤维蛋白-1与其假定受体αVβ3在肝血窦中共定位,但在胆管结构周围未共定位。