Lorent Kristin, Gong Weilong, Koo Kyung A, Waisbourd-Zinman Orith, Karjoo Sara, Zhao Xiao, Sealy Ian, Kettleborough Ross N, Stemple Derek L, Windsor Peter A, Whittaker Stephen J, Porter John R, Wells Rebecca G, Pack Michael
Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Department of Biological Sciences, University of the Sciences, Philadelphia, PA 19104, USA.
Sci Transl Med. 2015 May 6;7(286):286ra67. doi: 10.1126/scitranslmed.aaa1652.
Biliary atresia (BA) is a rapidly progressive and destructive fibrotic disorder of unknown etiology affecting the extrahepatic biliary tree of neonates. Epidemiological studies suggest that an environmental factor, such as a virus or toxin, is the cause of the disease, although none have been definitively established. Several naturally occurring outbreaks of BA in Australian livestock have been associated with the ingestion of unusual plants by pregnant animals during drought conditions. We used a biliary secretion assay in zebrafish to isolate a previously undescribed isoflavonoid, biliatresone, from Dysphania species implicated in a recent BA outbreak. This compound caused selective destruction of the extrahepatic, but not intrahepatic, biliary system of larval zebrafish. A mutation that enhanced biliatresone toxicity mapped to a region of the zebrafish genome that has conserved synteny with an established human BA susceptibility locus. The toxin also caused loss of cilia in neonatal mouse extrahepatic cholangiocytes in culture and disrupted cell polarity and monolayer integrity in cholangiocyte spheroids. Together, these findings provide direct evidence that BA could be initiated by perinatal exposure to an environmental toxin.
胆道闭锁(BA)是一种病因不明、迅速进展且具有破坏性的纤维化疾病,影响新生儿的肝外胆道系统。流行病学研究表明,环境因素,如病毒或毒素,是该疾病的病因,尽管尚未明确证实。澳大利亚家畜中几次自然发生的BA疫情与干旱期间怀孕动物摄入异常植物有关。我们利用斑马鱼的胆汁分泌试验,从与最近一次BA疫情有关的Dysphania物种中分离出一种先前未描述的异黄酮——胆闭锁素。这种化合物导致幼体斑马鱼的肝外而非肝内胆管系统发生选择性破坏。一个增强胆闭锁素毒性的突变定位于斑马鱼基因组中与已确定的人类BA易感位点具有保守同线性的区域。该毒素还导致培养的新生小鼠肝外胆管细胞中的纤毛丢失,并破坏胆管细胞球体中的细胞极性和单层完整性。这些发现共同提供了直接证据,表明BA可能由围产期接触环境毒素引发。