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Pathological Features of New Animal Models for Primary Biliary Cirrhosis

Primary biliary cirrhosis (PBC) is an autoimmune liver disease characterized by immune mediated biliary damage and frequent appearance of autoantibodies against mitochondrial enzymes. There is almost no useful animal model that is globally recognized and routinely used, however, several unique anima...

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Detalles Bibliográficos
Autores principales: Tsuneyama, Koichi, Moritoki, Yuki, Kikuchi, Kentaro, Nakanuma, Yasuni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3169354/
https://www.ncbi.nlm.nih.gov/pubmed/21994883
http://dx.doi.org/10.1155/2012/403954
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author Tsuneyama, Koichi
Moritoki, Yuki
Kikuchi, Kentaro
Nakanuma, Yasuni
author_facet Tsuneyama, Koichi
Moritoki, Yuki
Kikuchi, Kentaro
Nakanuma, Yasuni
author_sort Tsuneyama, Koichi
collection PubMed
description Primary biliary cirrhosis (PBC) is an autoimmune liver disease characterized by immune mediated biliary damage and frequent appearance of autoantibodies against mitochondrial enzymes. There is almost no useful animal model that is globally recognized and routinely used, however, several unique animal models manifested the characteristic clinical and pathological features of human PBC within the last 5 years. Herein, we compare the pathological features of previously reported and newly introduced novel animal models of PBC. Knowledge and understanding of the strengths and the limitations of each animal model have led to the development of promising therapies and novel tools to characterize these clinical conditions. Moreover, suitability of the model for the intended purpose should be confirmed by further research and analysis.
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spelling pubmed-31693542011-10-12 Pathological Features of New Animal Models for Primary Biliary Cirrhosis Tsuneyama, Koichi Moritoki, Yuki Kikuchi, Kentaro Nakanuma, Yasuni Int J Hepatol Review Article Primary biliary cirrhosis (PBC) is an autoimmune liver disease characterized by immune mediated biliary damage and frequent appearance of autoantibodies against mitochondrial enzymes. There is almost no useful animal model that is globally recognized and routinely used, however, several unique animal models manifested the characteristic clinical and pathological features of human PBC within the last 5 years. Herein, we compare the pathological features of previously reported and newly introduced novel animal models of PBC. Knowledge and understanding of the strengths and the limitations of each animal model have led to the development of promising therapies and novel tools to characterize these clinical conditions. Moreover, suitability of the model for the intended purpose should be confirmed by further research and analysis. Hindawi Publishing Corporation 2012 2011-07-06 /pmc/articles/PMC3169354/ /pubmed/21994883 http://dx.doi.org/10.1155/2012/403954 Text en Copyright © 2012 Koichi Tsuneyama et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Tsuneyama, Koichi
Moritoki, Yuki
Kikuchi, Kentaro
Nakanuma, Yasuni
Pathological Features of New Animal Models for Primary Biliary Cirrhosis
title Pathological Features of New Animal Models for Primary Biliary Cirrhosis
title_full Pathological Features of New Animal Models for Primary Biliary Cirrhosis
title_fullStr Pathological Features of New Animal Models for Primary Biliary Cirrhosis
title_full_unstemmed Pathological Features of New Animal Models for Primary Biliary Cirrhosis
title_short Pathological Features of New Animal Models for Primary Biliary Cirrhosis
title_sort pathological features of new animal models for primary biliary cirrhosis
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3169354/
https://www.ncbi.nlm.nih.gov/pubmed/21994883
http://dx.doi.org/10.1155/2012/403954
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