Tsuneyama K, Kono N, Yamashiro M, Kouda W, Sabit A, Sasaki M, Nakanuma Y
Second Department of Pathology, Kanazawa University School of Medicine, Kanazawa 920, Japan.
J Pathol. 1999 Dec;189(4):609-14. doi: 10.1002/(SICI)1096-9896(199912)189:4<609::AID-PATH474>3.0.CO;2-2.
Hepatolithiasis and primary sclerosing cholangitis (PSC) are intractable chronic biliary diseases. In hepatolithiasis, bilirubin-calcium stones are packed in multiple irregularly dilated intrahepatic bile ducts. In PSC, small bilirubin-calcium stones develop terminally. The progressive periductal fibrosis with dilated and stenotic bile ducts in these two diseases may play a role in their incurability. This immunohistochemical study has investigated the expression of some factors that might be involved in fibrogenesis in hepatolithiasis and PSC. Many mast cells positive for c-kit were found in the periductal and ductal fibrosis around the intrahepatic large bile ducts and also around the proliferative peribiliary glands. These mast cells also expressed basic fibroblast growth factor and/or tumour necrosis factor-alpha, which are known as fibrogenetic factors. It was of interest that the aberrant expression of stem cell factor (SCF), a ligand of c-kit, was demonstrated on biliary epithelia of the dilated and stenotic bile ducts showing periductal fibrosis and inflammation and also of the proliferated peribiliary glands in hepatolithiasis and PSC, while no such expression was seen in non-affected bile ducts in hepatolithiasis or in the bile ducts in normal livers. Some of the infiltrating mononuclear cells around the SCF-expressing bile ducts were also positive for SCF. It seems likely that aberrantly expressed SCF on biliary epithelial cells accumulates and stimulates mast cells via the c-kit receptor and that these up-regulated mast cells induce progressive periductal and portal fibrosis by displaying fibrogenetic factors in hepatolithiasis and PSC.
肝内胆管结石和原发性硬化性胆管炎(PSC)是难治性慢性胆道疾病。在肝内胆管结石中,胆红素钙结石堆积在多个不规则扩张的肝内胆管中。在PSC中,小的胆红素钙结石在疾病终末期形成。这两种疾病中伴有胆管扩张和狭窄的进行性胆管周围纤维化可能是其难以治愈的原因之一。本免疫组化研究调查了一些可能参与肝内胆管结石和PSC纤维化形成的因子的表达情况。在肝内大胆管周围以及增生的胆管周围腺体周围的胆管周围和导管纤维化区域发现了许多c-kit阳性的肥大细胞。这些肥大细胞还表达碱性成纤维细胞生长因子和/或肿瘤坏死因子-α,这些都是已知的促纤维化因子。有趣的是,在肝内胆管结石和PSC中,显示胆管周围纤维化和炎症的扩张和狭窄胆管的胆管上皮以及增生的胆管周围腺体上,证实了干细胞因子(SCF)(c-kit的配体)的异常表达,而在肝内胆管结石未受影响的胆管或正常肝脏的胆管中未观察到这种表达。表达SCF的胆管周围一些浸润的单核细胞也呈SCF阳性。似乎胆管上皮细胞上异常表达的SCF会积累并通过c-kit受体刺激肥大细胞,并且这些上调的肥大细胞通过在肝内胆管结石和PSC中显示促纤维化因子来诱导进行性胆管周围和门静脉纤维化。