Department of Pediatric Surgery, Children's Hospital of Fudan University, Shanghai Key Laboratory of Birth Defect, and Key Laboratory of Neonatal Disease, Ministry of Health, 399 Wan Yuan Road, Shanghai, 201102, China.
Lab Invest. 2020 Nov;100(11):1425-1435. doi: 10.1038/s41374-020-0467-7. Epub 2020 Jul 17.
Exposure to environmental toxins may be responsible for biliary atresia. The focus of this study was to investigate the effect of biliatresone on the development of the hepatobiliary system in mice. We successfully synthesized biliatresone with a purity of 98% and confirmed its biliary toxicity. Exposure to high doses of biliatresone caused abortion or death in pregnant mice. Neonatal mice injected with biliatresone developed clinical signs of biliary obstruction, and dysplasia or the absence of extrahepatic biliary tract lumen, which confirmed the occurrence of biliary atresia. In the portal tract of biliary atresia mice, signs of infiltration of inflammatory cells and liver fibrosis were observed. The signature of extrahepatic biliary gene expression in these mice mainly involved the cell adhesion process, and hepatic RNA-seq was highly linked to transcriptional evidence of oxidative stress. When compared with the control group, hepatic glutathione levels were markedly reduced after biliatresone injection. Taken together, these data confirm that biliatresone causes severe developmental abnormalities of the hepatobiliary system in mice. Furthermore, decreased levels of glutathione may play a mechanistic role in the pathogenesis of liver fibrosis in biliatresone-induced experimental biliary atresia.
暴露于环境毒素可能是导致先天性胆道闭锁的原因。本研究的重点是探讨胆甾烷醇酮对小鼠肝胆系统发育的影响。我们成功合成了纯度为 98%的胆甾烷醇酮,并证实了其胆毒性。高剂量的胆甾烷醇酮暴露会导致怀孕小鼠流产或死亡。注射胆甾烷醇酮的新生小鼠出现胆汁阻塞的临床症状,肝外胆管腔出现发育不良或缺失,证实发生了先天性胆道闭锁。在胆道闭锁小鼠的门脉区,观察到炎症细胞浸润和肝纤维化的迹象。这些小鼠的肝外胆管基因表达特征主要涉及细胞黏附过程,肝 RNA-seq 与氧化应激的转录证据高度相关。与对照组相比,注射胆甾烷醇酮后肝谷胱甘肽水平明显降低。综上所述,这些数据证实胆甾烷醇酮可导致小鼠肝胆系统严重发育异常。此外,谷胱甘肽水平降低可能在胆甾烷醇酮诱导的实验性先天性胆道闭锁肝纤维化发病机制中起作用。