Beta-amyloid deposition around hepatic bile ducts is a novel pathobiological and diagnostic feature of biliary atresia

Biliary atresia (BA) is a poorly understood and devastating obstructive bile duct disease of newborns. It is often diagnosed late, is incurable and frequently requires liver transplantation. In this study, we aimed to investigate the underlying pathogenesis and molecular signatures associated with B...

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Veröffentlicht in:Journal of hepatology 2020-12, Vol.73 (6), p.1391-1403
Hauptverfasser: Babu, Rosana Ottakandathil, Lui, Vincent Chi Hang, Chen, Yan, Yiu, Rachel Sze Wan, Ye, Yongqin, Niu, Ben, Wu, Zhongluan, Zhang, Ruizhong, Yu, Michelle On Na, Chung, Patrick Ho Yu, Wong, Kenneth Kak Yuen, Xia, Huimin, Zhang, Michael Qi, Wang, Bin, Lendahl, Urban, Tam, Paul Kwong Hang
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container_end_page 1403
container_issue 6
container_start_page 1391
container_title Journal of hepatology
container_volume 73
creator Babu, Rosana Ottakandathil
Lui, Vincent Chi Hang
Chen, Yan
Yiu, Rachel Sze Wan
Ye, Yongqin
Niu, Ben
Wu, Zhongluan
Zhang, Ruizhong
Yu, Michelle On Na
Chung, Patrick Ho Yu
Wong, Kenneth Kak Yuen
Xia, Huimin
Zhang, Michael Qi
Wang, Bin
Lendahl, Urban
Tam, Paul Kwong Hang
description Biliary atresia (BA) is a poorly understood and devastating obstructive bile duct disease of newborns. It is often diagnosed late, is incurable and frequently requires liver transplantation. In this study, we aimed to investigate the underlying pathogenesis and molecular signatures associated with BA. We combined organoid and transcriptomic analysis to gain new insights into BA pathobiology using patient samples and a mouse model of BA. Liver organoids derived from patients with BA and a rhesus rotavirus A-infected mouse model of BA, exhibited aberrant morphology and disturbed apical-basal organization. Transcriptomic analysis of BA organoids revealed a shift from cholangiocyte to hepatocyte transcriptional signatures and altered beta-amyloid-related gene expression. Beta-amyloid accumulation was observed around the bile ducts in BA livers and exposure to beta-amyloid induced the aberrant morphology in control organoids. The novel observation that beta-amyloid accumulates around bile ducts in the livers of patients with BA has important pathobiological implications, as well as diagnostic potential. Biliary atresia is a poorly understood and devastating obstructive bile duct disease of newborns. It is often diagnosed late, is incurable and frequently requires liver transplantation. Using human and mouse ‘liver mini-organs in the dish’, we unexpectedly identified beta-amyloid deposition – the main pathological feature of Alzheimer's disease and cerebral amyloid angiopathy – around bile ducts in livers from patients with biliary atresia. This finding reveals a novel pathogenic mechanism that could have important diagnostic and therapeutic implications. [Display omitted] •Liver organoids from patients with BA exhibited aberrant morphology and disturbed apical-basal organization.•Transcriptomic analysis of BA organoids revealed a shift from cholangiocyte to hepatocyte transcriptional signatures.•Beta-amyloid accumulation was observed around the bile ducts in BA livers.•Exposure to beta-amyloid induced aberrant morphology in control organoids.•Beta-amyloid accumulation represents a novel finding with pathobiological implications and diagnostic potential for BA.
doi_str_mv 10.1016/j.jhep.2020.06.012
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It is often diagnosed late, is incurable and frequently requires liver transplantation. In this study, we aimed to investigate the underlying pathogenesis and molecular signatures associated with BA. We combined organoid and transcriptomic analysis to gain new insights into BA pathobiology using patient samples and a mouse model of BA. Liver organoids derived from patients with BA and a rhesus rotavirus A-infected mouse model of BA, exhibited aberrant morphology and disturbed apical-basal organization. Transcriptomic analysis of BA organoids revealed a shift from cholangiocyte to hepatocyte transcriptional signatures and altered beta-amyloid-related gene expression. Beta-amyloid accumulation was observed around the bile ducts in BA livers and exposure to beta-amyloid induced the aberrant morphology in control organoids. The novel observation that beta-amyloid accumulates around bile ducts in the livers of patients with BA has important pathobiological implications, as well as diagnostic potential. Biliary atresia is a poorly understood and devastating obstructive bile duct disease of newborns. It is often diagnosed late, is incurable and frequently requires liver transplantation. Using human and mouse ‘liver mini-organs in the dish’, we unexpectedly identified beta-amyloid deposition – the main pathological feature of Alzheimer's disease and cerebral amyloid angiopathy – around bile ducts in livers from patients with biliary atresia. This finding reveals a novel pathogenic mechanism that could have important diagnostic and therapeutic implications. [Display omitted] •Liver organoids from patients with BA exhibited aberrant morphology and disturbed apical-basal organization.•Transcriptomic analysis of BA organoids revealed a shift from cholangiocyte to hepatocyte transcriptional signatures.•Beta-amyloid accumulation was observed around the bile ducts in BA livers.•Exposure to beta-amyloid induced aberrant morphology in control organoids.•Beta-amyloid accumulation represents a novel finding with pathobiological implications and diagnostic potential for BA.</description><identifier>ISSN: 0168-8278</identifier><identifier>ISSN: 1600-0641</identifier><identifier>EISSN: 1600-0641</identifier><identifier>DOI: 10.1016/j.jhep.2020.06.012</identifier><identifier>PMID: 32553668</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Alzheimer's disease ; Amyloid ; Bile ; Bile duct ; Bile ducts ; Biliary atresia ; Cerebral amyloid angiopathy ; Cholangiopathy ; Gene expression ; Liver ; Liver disease ; Liver transplantation ; Medicin och hälsovetenskap ; Morphology ; Neonates ; Neurodegenerative diseases ; Organoid ; Organoids ; Rotavirus ; Transcription ; Transplantation ; β-Amyloid</subject><ispartof>Journal of hepatology, 2020-12, Vol.73 (6), p.1391-1403</ispartof><rights>2020 European Association for the Study of the Liver</rights><rights>Copyright © 2020 European Association for the Study of the Liver. 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It is often diagnosed late, is incurable and frequently requires liver transplantation. In this study, we aimed to investigate the underlying pathogenesis and molecular signatures associated with BA. We combined organoid and transcriptomic analysis to gain new insights into BA pathobiology using patient samples and a mouse model of BA. Liver organoids derived from patients with BA and a rhesus rotavirus A-infected mouse model of BA, exhibited aberrant morphology and disturbed apical-basal organization. Transcriptomic analysis of BA organoids revealed a shift from cholangiocyte to hepatocyte transcriptional signatures and altered beta-amyloid-related gene expression. Beta-amyloid accumulation was observed around the bile ducts in BA livers and exposure to beta-amyloid induced the aberrant morphology in control organoids. The novel observation that beta-amyloid accumulates around bile ducts in the livers of patients with BA has important pathobiological implications, as well as diagnostic potential. Biliary atresia is a poorly understood and devastating obstructive bile duct disease of newborns. It is often diagnosed late, is incurable and frequently requires liver transplantation. Using human and mouse ‘liver mini-organs in the dish’, we unexpectedly identified beta-amyloid deposition – the main pathological feature of Alzheimer's disease and cerebral amyloid angiopathy – around bile ducts in livers from patients with biliary atresia. This finding reveals a novel pathogenic mechanism that could have important diagnostic and therapeutic implications. [Display omitted] •Liver organoids from patients with BA exhibited aberrant morphology and disturbed apical-basal organization.•Transcriptomic analysis of BA organoids revealed a shift from cholangiocyte to hepatocyte transcriptional signatures.•Beta-amyloid accumulation was observed around the bile ducts in BA livers.•Exposure to beta-amyloid induced aberrant morphology in control organoids.•Beta-amyloid accumulation represents a novel finding with pathobiological implications and diagnostic potential for BA.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>32553668</pmid><doi>10.1016/j.jhep.2020.06.012</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0001-9543-8141</orcidid><orcidid>https://orcid.org/0000-0001-7371-503X</orcidid><orcidid>https://orcid.org/0000-0003-2414-7990</orcidid><orcidid>https://orcid.org/0000-0001-6231-3035</orcidid><oa>free_for_read</oa></addata></record>
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subjects Alzheimer's disease
Amyloid
Bile
Bile duct
Bile ducts
Biliary atresia
Cerebral amyloid angiopathy
Cholangiopathy
Gene expression
Liver
Liver disease
Liver transplantation
Medicin och hälsovetenskap
Morphology
Neonates
Neurodegenerative diseases
Organoid
Organoids
Rotavirus
Transcription
Transplantation
β-Amyloid
title Beta-amyloid deposition around hepatic bile ducts is a novel pathobiological and diagnostic feature of biliary atresia
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