Division of Gastroenterology, Department of Medicine, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, United States.
Division of Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, PA, United States.
J Hepatol. 2020 Jan;72(1):135-145. doi: 10.1016/j.jhep.2019.08.036. Epub 2019 Sep 25.
BACKGROUND & AIMS: The extrahepatic bile duct is the primary tissue initially affected by biliary atresia. Biliary atresia is a cholangiopathy which exclusively affects neonates. Current animal models suggest that the developing bile duct is uniquely susceptible to damage. In this study, we aimed to define the anatomical and functional differences between the neonatal and adult mouse extrahepatic bile ducts.
We studied mouse passaged cholangiocytes, mouse BALB/c neonatal and adult primary cholangiocytes, as well as isolated extrahepatic bile ducts, and a collagen reporter mouse. The methods used included transmission electron microscopy, lectin staining, immunostaining, rhodamine uptake assays, bile acid toxicity assays, and in vitro modeling of the matrix.
The cholangiocyte monolayer of the neonatal extrahepatic bile duct was immature, lacking the uniform apical glycocalyx and mature cell-cell junctions typical of adult cholangiocytes. Functional studies showed that the glycocalyx protected against bile acid injury and that neonatal cholangiocyte monolayers were more permeable than adult monolayers. In adult ducts, the submucosal space was filled with collagen I, elastin, hyaluronic acid, and proteoglycans. In contrast, the neonatal submucosa had little collagen I and elastin, although both increased rapidly after birth. In vitro modeling of the matrix suggested that the composition of the neonatal submucosa relative to the adult submucosa led to increased diffusion of bile. A Col-GFP reporter mouse showed that cells in the neonatal but not adult submucosa were actively producing collagen.
We identified 4 key differences between the neonatal and adult extrahepatic bile duct. We showed that these features may have functional implications, suggesting the neonatal extrahepatic bile ducts are particularly susceptible to injury and fibrosis.
Biliary atresia is a disease that affects newborns and is characterized by extrahepatic bile duct injury and obstruction, resulting in liver injury. We identify 4 key differences between the epithelial and submucosal layers of the neonatal and adult extrahepatic bile duct and show that these may render the neonatal duct particularly susceptible to injury.
肝外胆管是先天性胆道闭锁(biliary atresia)首先受累的组织。先天性胆道闭锁是一种专属于新生儿的胆管疾病。目前的动物模型表明,发育中的胆管特别容易受到损伤。在这项研究中,我们旨在定义新生鼠和成年鼠肝外胆管的解剖和功能差异。
我们研究了传代的鼠胆管细胞、新生鼠和成年鼠原代胆管细胞、以及分离的肝外胆管和胶原报告鼠。使用的方法包括透射电子显微镜、凝集素染色、免疫染色、罗丹明摄取试验、胆汁酸毒性试验和体外基质建模。
新生鼠肝外胆管的胆管细胞单层不成熟,缺乏成年胆管细胞典型的均匀顶糖萼和成熟的细胞-细胞连接。功能研究表明,糖萼可防止胆汁酸损伤,且新生鼠胆管细胞单层的通透性高于成年单层。在成年胆管中,黏膜下层充满了胶原 I、弹性蛋白、透明质酸和糖胺聚糖。相比之下,新生鼠的黏膜下层几乎没有胶原 I 和弹性蛋白,但出生后迅速增加。体外基质建模表明,与成年黏膜下层相比,新生黏膜下层的组成导致胆汁扩散增加。Col-GFP 报告鼠显示,新生而非成年黏膜下层的细胞在积极合成胶原。
我们确定了新生鼠和成年鼠肝外胆管之间的 4 个关键差异。我们表明,这些特征可能具有功能意义,提示新生鼠肝外胆管特别容易受到损伤和纤维化。
先天性胆道闭锁是一种影响新生儿的疾病,其特征为肝外胆管损伤和阻塞,导致肝脏损伤。我们确定了新生鼠和成年鼠肝外胆管的上皮和黏膜下层之间的 4 个关键差异,并表明这些差异可能使新生胆管特别容易受到损伤。