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一种导致胆道闭锁的植物异黄酮的鉴定。

Identification of a plant isoflavonoid that causes biliary atresia.

作者信息

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

机构信息

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.

出版信息

Sci Transl Med. 2015 May 6;7(286):286ra67. doi: 10.1126/scitranslmed.aaa1652.

DOI:10.1126/scitranslmed.aaa1652
PMID:25947162
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4784984/
Abstract

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.

摘要

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。

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本文引用的文献

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On Congenital Obliteration of the Bile-Ducts.论先天性胆管闭锁
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Identification of Annexin A4 as a hepatopancreas factor involved in liver cell survival.鉴定膜联蛋白A4作为参与肝细胞存活的肝胰腺因子。
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PLoS Pathog. 2014 Mar 20;10(3):e1004011. doi: 10.1371/journal.ppat.1004011. eCollection 2014 Mar.
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Gene expression signature for biliary atresia and a role for interleukin-8 in pathogenesis of experimental disease.胆道闭锁的基因表达特征和白细胞介素-8在实验性疾病发病机制中的作用。
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Replication of a GWAS signal in a Caucasian population implicates ADD3 in susceptibility to biliary atresia.GWAS 信号在高加索人群中的复制提示 ADD3 基因与先天性胆道闭锁的易感性相关。
Hum Genet. 2014 Feb;133(2):235-43. doi: 10.1007/s00439-013-1368-2. Epub 2013 Oct 9.
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B cell deficient mice are protected from biliary obstruction in the rotavirus-induced mouse model of biliary atresia.B 细胞缺陷小鼠在轮状病毒诱导的胆道闭锁小鼠模型中可免受胆道阻塞的影响。
PLoS One. 2013 Aug 21;8(8):e73644. doi: 10.1371/journal.pone.0073644. eCollection 2013.
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Associations of mitochondrial haplogroups b4 and e with biliary atresia and differential susceptibility to hydrophobic bile Acid.线粒体单倍群 b4 和 e 与胆道闭锁的关联及对疏水性胆汁酸的不同易感性。
PLoS Genet. 2013;9(8):e1003696. doi: 10.1371/journal.pgen.1003696. Epub 2013 Aug 15.
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Common genetic variants regulating ADD3 gene expression alter biliary atresia risk.常见调节 ADD3 基因表达的遗传变异可改变先天性胆道闭锁的风险。
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Chromatin and epigenetic features of long-range gene regulation.染色质和长距离基因调控的表观遗传特征。
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