Sirica A E
Department of Pathology, Medical College of Virginia, Virginia Commonwealth University, Richmond 23298-0297, USA.
Toxicol Pathol. 1996 Jan-Feb;24(1):90-9. doi: 10.1177/019262339602400113.
Distinctive intrahepatic biliary adaptation responses occur in the liver of rats subjected to select hepatotoxic and/or carcinogenic treatments with the nongenotoxic cholangiocarcinogenic agent furan. Specifically, metaplastic small intestinal-like glands closely resembling in their cellular composition the crypts of Lieberkühn of normal rat small intestine were selectively derived from putative hyperplastic bile ductule-like progenitor structures in the right and caudate liver lobes of young adult Fischer-344 male rats given furan by gavage at a daily dose of 30-45 mg/kg body weight, 5 times weekly, over a 2-6-wk treatment period. Longer term chronic administration of furan at 30 mg/kg/day for 9-19 wk resulted in the preferential development of primary hepatic adenocarcinomas, which arose at 70-100% incidences from right/caudate liver lobes and which were characterized by small intestine mucosal cell differentiation. Interestingly, the neoplastic glands of these "intestinal-type" hapatic tumors demonstrated strongly positive immunochemical reactions for both hepatocyte growth factor/scatter factor and its c-met encoded receptor and were immunohistochemically positive for transforming growth factor beta 1 (TGF-beta 1) and for mannose-6-phosphate/insulin-like growth factor II receptor, implicated in the activation of latent TGF-beta 1. In contrast, a different pattern of aberrant bile ductular cell differentiation was noted to occur in the atrophied right liver lobe of moribund Fischer-344 male rats that were chronically exposed over a 10-14-day period to a severely hepatotoxic dose of furan (60 mg/kg/day). Under this latter experimental condition, rare yet distinct cholangiolar-like structures composed of biliary epithelial cells and typically a single ductular hepatocytic cell in various stages of maturation specifically formed in association with an extensive hyperplastic bile ductular reaction. Very similar cholangiolar-like structures also appeared in areas of preexisting hyperplastic bile ductule tissue at 3-5 days following the administration of a single hepatonecrogenic dose of CCl4 to rats that 4-6 wk earlier had been subjected to a bile duct ligation. In addition, a novel rat model was developed in which furan combined in a unique synergistic manner with bile duct ligation to induce the replacement of almost all of liver with well-differentiated hyperplastic bile ductules without evidence of differentiation along either metaplastic small intestine mucosal cell or ductular hepatocyte lineages. Bile ductular epithelial cell isolated from bile duct-ligated/furan-treated rats were further observed to be organized in the form of bile duct-like structures in vitro under specific conditions of primary cell culture and in vivo following their cell transplantation into the inguinal fat pads of sygeneic recipient rats. Overall, these findings serve to exemplify the remarkable plasticity that may be exhibited by certain proliferating biliary cell populations in liver in response to specific types of severe hepatic injury and/or during cholangiocarcinogenesis.
在用非基因毒性胆管致癌剂呋喃进行选择性肝毒性和/或致癌处理的大鼠肝脏中,会出现独特的肝内胆管适应性反应。具体而言,在年轻成年Fischer-344雄性大鼠的右肝叶和尾状肝叶中,假定的增生性胆小管样祖细胞结构会选择性地衍生出化生的小肠样腺体,这些腺体的细胞组成与正常大鼠小肠的利伯kühn隐窝极为相似。这些大鼠通过灌胃给予呋喃,每日剂量为30 - 45 mg/kg体重,每周5次,持续2 - 6周的治疗期。长期以30 mg/kg/天的剂量慢性给予呋喃9 - 19周,会导致原发性肝腺癌的优先发展,这些肿瘤在右/尾状肝叶的发生率为70 - 100%,其特征是小肠黏膜细胞分化。有趣的是,这些“肠型”肝肿瘤的肿瘤腺体对肝细胞生长因子/散射因子及其c-met编码受体均表现出强烈的免疫化学反应,并且对转化生长因子β1(TGF-β1)和甘露糖-6-磷酸/胰岛素样生长因子II受体免疫组化呈阳性,这些受体与潜在TGF-β1的激活有关。相比之下,在濒死的Fischer-344雄性大鼠萎缩的右肝叶中,观察到一种不同的异常胆小管细胞分化模式,这些大鼠在10 - 14天的时间内长期暴露于严重肝毒性剂量的呋喃(60 mg/kg/天)。在这种实验条件下,由胆管上皮细胞和通常处于不同成熟阶段的单个胆小管肝细胞组成的罕见但独特的胆小管样结构,特别与广泛的增生性胆小管反应相关形成。在给大鼠单次给予肝坏死剂量的CCl4(4 - 6周前已进行胆管结扎)后的3 - 5天,在先前存在的增生性胆小管组织区域也出现了非常相似的胆小管样结构。此外,还建立了一种新型大鼠模型,其中呋喃与胆管结扎以独特的协同方式联合使用,可诱导几乎整个肝脏被高度分化的增生性胆小管替代,且没有沿化生的小肠黏膜细胞或胆小管肝细胞谱系分化的证据。从胆管结扎/呋喃处理的大鼠中分离出的胆管上皮细胞,在原代细胞培养的特定条件下,体外观察到它们以胆管样结构的形式组织起来,并且在将其细胞移植到同基因受体大鼠的腹股沟脂肪垫后,在体内也观察到了这种情况。总体而言,这些发现例证了肝脏中某些增殖性胆管细胞群体在应对特定类型的严重肝损伤和/或胆管癌发生过程中可能表现出的显著可塑性。