Identification of a plant isoflavonoid that causes biliary atresia

被引:96
|
作者
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
机构
[1] Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, 19104, PA
[2] Department of Biological Sciences, University of the Sciences, Philadelphia, 19104, PA
[3] Division of Pediatric Gastroenterology, Hepatology, and Nutrition, Children's Hospital of Philadelphia, Philadelphia, 19104, PA
[4] Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv
[5] Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge
[6] Faculty of Veterinary Science, University of Sydney, Camden, 2570, NSW
[7] Hume Livestock Health and Pest Authority, Albury, 2640, NSW
[8] Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, 19104, PA
[9] Cell and Developmental Biology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, 19104, PA
基金
英国惠康基金;
关键词
D O I
10.1126/scitranslmed.aaa1652
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
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