Elmore L W, Sirica A E
Department of Pathology, Medical College of Virginia, Virginia Commonwealth University, Richmond 23298.
Cancer Res. 1991 Oct 15;51(20):5752-9.
In order to investigate the early cellular changes in liver associated with furan cholangiocarcinogenesis, young adult male Fischer 344 rats were administered furan by gavage once a day, 5 days a wk for 2 to 3 wk at doses ranging from 15 to 60 mg/kg of body weight per day. The most conspicuous feature observed in the liver of animals receiving the higher doses of furan was a rapidly developed cholangiofibrosis characterized by the presence of bile ductular hyperplasia, intestinal metaplasia, and fibrosis. Moreover, this lesion was found to be almost exclusively localized to the caudate liver lobe, which by morphometric analysis was further determined to be largely replaced by cholangiofibrotic tissue. Both the hyperplastic bile ductular epithelial cells and the intestinal-like epithelial cells in these areas selectively exhibited a strongly positive immunohistochemical staining for cytokeratin 19 and were supported by well-developed basement membranes enriched in both laminin and type IV collagen. However, in contrast to the hyperplastic bile ductules, electron microscopy of the metaplastic intestinal glands revealed them to be composed mostly of columnar epithelial cells with well-developed striated borders, less numerous mucin-secreting goblet cells, and occasional neuroendocrine-like cells, thus closely resembling in their cellular composition that of intestinal mucosa. These metaplastic glands also showed a more heterogeneous pattern of staining for both gamma-glutamyl transpeptidase and the placental form of glutathione S-transferase than did the hyperplastic bile ductules. At the 60-mg/kg/day furan dose, cholangiolar-like structures composed of biliary epithelial cells and ductular hepatocytic cells at different stages of morphological differentiation were also observed. Phenotypically, the biliary epithelial and "ductular hepatocytes" of these cholangioles shared a common basement membrane containing laminin and type IV collagen, as well as a luminal plasma membrane gamma-glutamyl transpeptidase. On the other hand, only the biliary epithelial cells of the newly appearing mixed cell cholangioles stained positive for cytokeratin 19. Interestingly, unlike hepatocarcinogen-induced oval cells, alpha-fetoprotein expression was not detected in any of the cell types comprising the furan-induced cholangiofibrotic tissue. These results support a novel in vivo model for investigating cell lineages in the development in liver of intestinal metaplasia, "ductular hepatocytes," and cholangiofibrosis in relation to intrahepatic cholangiocarcinogenesis.
为了研究与呋喃诱导的胆管癌发生相关的肝脏早期细胞变化,对年轻成年雄性Fischer 344大鼠每天经口灌胃给予呋喃,每周5天,持续2至3周,剂量范围为每天15至60毫克/千克体重。在接受较高剂量呋喃的动物肝脏中观察到的最显著特征是迅速发展的胆管纤维化,其特征为胆小管增生、肠化生和纤维化。此外,该病变几乎仅局限于肝尾状叶,通过形态计量分析进一步确定该叶大部分被胆管纤维组织取代。这些区域中增生的胆小管上皮细胞和肠样上皮细胞均选择性地对细胞角蛋白19呈现强阳性免疫组化染色,并由富含层粘连蛋白和IV型胶原的发育良好的基底膜支持。然而,与增生的胆小管不同,化生的肠腺的电子显微镜检查显示它们主要由具有发达纹状缘的柱状上皮细胞、数量较少的分泌粘蛋白的杯状细胞和偶尔的神经内分泌样细胞组成,因此其细胞组成与肠黏膜非常相似。这些化生的腺体在γ-谷氨酰转肽酶和胎盘型谷胱甘肽S-转移酶的染色模式上也比增生的胆小管表现出更多的异质性。在每天60毫克/千克的呋喃剂量下,还观察到由处于不同形态分化阶段的胆管上皮细胞和胆小管肝细胞组成的胆小管样结构。从表型上看,这些胆小管的胆管上皮细胞和“胆小管肝细胞”共享一个包含层粘连蛋白和IV型胶原的共同基底膜,以及腔面膜γ-谷氨酰转肽酶。另一方面,新出现的混合细胞胆小管中只有胆管上皮细胞对细胞角蛋白19染色呈阳性。有趣的是,与肝癌致癌物诱导的卵圆细胞不同,在构成呋喃诱导的胆管纤维组织的任何细胞类型中均未检测到甲胎蛋白表达。这些结果支持了一种新的体内模型,用于研究肠化生、“胆小管肝细胞”和胆管纤维化在肝内胆管癌发生过程中的细胞谱系发育。