Roskams T, van den Oord J J, De Vos R, Desmet V J
Department of Pathology, University Hospital St. Rafaël, Catholic University of Leuven, Belgium.
Am J Pathol. 1990 Nov;137(5):1019-25.
Various cholestatic liver diseases are accompanied by a striking increase in the number of bile ductules. This so-called ductular reaction is thought to arise both from ductular metaplasia of hepatocytes and from proliferation of pre-existing bile ductules. Previous studies have shown that these reactive bile ductules differ from their normal counterpart in enzyme and immunohistochemical make-up. Using monoclonal antibodies directed to neuroendocrine markers and immunohistochemistry, we found that reactive bile ductules in cholestatic liver disease display neuroendocrine features. In all cases of primary biliary cirrhosis (PBC), primary sclerosing cholangitis (PSC), extrahepatic obstruction, and acute hepatitis A, reactive bile ductules expressed the neural cell adhesion molecule (N-CAM) and reacted with monoclonal antibody A2B5. Both N-CAM and the ganglioside, recognized by A2B5, are restricted to neuroendocrine cells and tissues. In all but four of these cases, the same bile ductules expressed chromogranin-A, present in the matrix of neuroendocrine granules. Furthermore, in three cases of longstanding cholestasis, scattered periportal hepatocytes expressed chromogranin-A but not N-CAM. Other neuroendocrine markers such as neuron-specific enolase, synaptophysin, or myelin-associated glycoprotein were lacking from both bile ductules and hepatocytes. The neuroendocrine phenotype of bile ductules and hepatocytes was confirmed on electronmicroscopy, demonstrating various numbers of dense-cored, neuroendocrine granules near the peripheral cell membrane in bile ductules as well as in cells intermediate between hepatocytes and bile ductular cells. In 10 cases of normal liver tissue without ductular reaction, bile ductules lacked neuroendocrine markers except in two cases in which very weak reactivity for chromogranin-A was observed. These findings illustrate the presence of a new, neuroendocrine cell type that emerges in the liver during cholestasis. Elucidation of the significance of the neuroendocrine substance(s) produced in the dense cored granules of reactive bile ductules awaits their isolation and characterization. We can speculate that this molecule plays an autocrine or paracrine regulatory role in the process of ductular metaplasia of hepatocytes or growth of bile ductules.
各种胆汁淤积性肝病都伴随着胆小管数量的显著增加。这种所谓的胆管反应被认为既源于肝细胞的胆管化生,也源于原有胆小管的增殖。先前的研究表明,这些反应性胆小管在酶和免疫组化组成上与其正常对应物不同。使用针对神经内分泌标志物的单克隆抗体和免疫组化技术,我们发现胆汁淤积性肝病中的反应性胆小管具有神经内分泌特征。在原发性胆汁性肝硬化(PBC)、原发性硬化性胆管炎(PSC)、肝外梗阻和急性甲型肝炎的所有病例中,反应性胆小管表达神经细胞黏附分子(N-CAM)并与单克隆抗体A2B5发生反应。N-CAM和A2B5识别的神经节苷脂都仅限于神经内分泌细胞和组织。在除4例之外的所有这些病例中,同样的胆小管表达嗜铬粒蛋白-A,其存在于神经内分泌颗粒的基质中。此外,在3例长期胆汁淤积病例中,散在的汇管区周围肝细胞表达嗜铬粒蛋白-A但不表达N-CAM。胆小管和肝细胞均缺乏其他神经内分泌标志物,如神经元特异性烯醇化酶、突触素或髓鞘相关糖蛋白。胆小管和肝细胞的神经内分泌表型在电子显微镜下得到证实,显示胆小管以及肝细胞和胆小管细胞之间的中间细胞的外周细胞膜附近有不同数量的致密核心神经内分泌颗粒。在10例无胆管反应的正常肝组织病例中,胆小管缺乏神经内分泌标志物,只有2例观察到对嗜铬粒蛋白-A的非常微弱的反应。这些发现说明了在胆汁淤积期间肝脏中出现了一种新的神经内分泌细胞类型。阐明反应性胆小管致密核心颗粒中产生的神经内分泌物质的意义有待于对其进行分离和鉴定。我们可以推测,这种分子在肝细胞的胆管化生过程或胆小管生长过程中发挥自分泌或旁分泌调节作用。