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Biliary Atresia – emerging diagnostic and therapy opportunities()

Biliary Atresia is a devastating pediatric cholangiopathy affecting the bile ducts of the liver. In this review, we describe recent progress in the understanding of liver development with a focus on cholangiocyte differentiation and how use of technical platforms, including rodent, zebrafish and org...

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Detalles Bibliográficos
Autores principales: Lendahl, Urban, Lui, Vincent C.H., Chung, Patrick H.Y., Tam, Paul K.H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8604670/
https://www.ncbi.nlm.nih.gov/pubmed/34781099
http://dx.doi.org/10.1016/j.ebiom.2021.103689
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author Lendahl, Urban
Lui, Vincent C.H.
Chung, Patrick H.Y.
Tam, Paul K.H.
author_facet Lendahl, Urban
Lui, Vincent C.H.
Chung, Patrick H.Y.
Tam, Paul K.H.
author_sort Lendahl, Urban
collection PubMed
description Biliary Atresia is a devastating pediatric cholangiopathy affecting the bile ducts of the liver. In this review, we describe recent progress in the understanding of liver development with a focus on cholangiocyte differentiation and how use of technical platforms, including rodent, zebrafish and organoid models, advances our understanding of Biliary Atresia. This is followed by a description of potential pathomechanisms, such as autoimmune responses, inflammation, disturbed apical-basal cell polarity, primary cilia dysfunction as well as beta-amyloid accumulation. Finally, we describe current and emerging diagnostic opportunities and recent translation breakthroughs for Biliary Atresia in the area of emerging therapy development, including immunomodulation and organoid-based systems for liver and bile duct repair.
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spelling pubmed-86046702021-11-24 Biliary Atresia – emerging diagnostic and therapy opportunities() Lendahl, Urban Lui, Vincent C.H. Chung, Patrick H.Y. Tam, Paul K.H. EBioMedicine Review Biliary Atresia is a devastating pediatric cholangiopathy affecting the bile ducts of the liver. In this review, we describe recent progress in the understanding of liver development with a focus on cholangiocyte differentiation and how use of technical platforms, including rodent, zebrafish and organoid models, advances our understanding of Biliary Atresia. This is followed by a description of potential pathomechanisms, such as autoimmune responses, inflammation, disturbed apical-basal cell polarity, primary cilia dysfunction as well as beta-amyloid accumulation. Finally, we describe current and emerging diagnostic opportunities and recent translation breakthroughs for Biliary Atresia in the area of emerging therapy development, including immunomodulation and organoid-based systems for liver and bile duct repair. Elsevier 2021-11-12 /pmc/articles/PMC8604670/ /pubmed/34781099 http://dx.doi.org/10.1016/j.ebiom.2021.103689 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Review
Lendahl, Urban
Lui, Vincent C.H.
Chung, Patrick H.Y.
Tam, Paul K.H.
Biliary Atresia – emerging diagnostic and therapy opportunities()
title Biliary Atresia – emerging diagnostic and therapy opportunities()
title_full Biliary Atresia – emerging diagnostic and therapy opportunities()
title_fullStr Biliary Atresia – emerging diagnostic and therapy opportunities()
title_full_unstemmed Biliary Atresia – emerging diagnostic and therapy opportunities()
title_short Biliary Atresia – emerging diagnostic and therapy opportunities()
title_sort biliary atresia – emerging diagnostic and therapy opportunities()
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8604670/
https://www.ncbi.nlm.nih.gov/pubmed/34781099
http://dx.doi.org/10.1016/j.ebiom.2021.103689
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