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Immunohistochemical evaluation of hepatic progenitor cells in different types of feline liver diseases

Hepatic progenitor cells are periportally resident cells capable of differentiating into mature hepatocytes or cholangiocytes to ensure hepatic regeneration. This reaction is termed a ductular reaction. In the present study, regenerative response of the feline liver to different hepatic diseases was...

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Autores principales: ABOU MONSEF, Yanad, KUTSAL, Osman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Veterinary Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8111336/
https://www.ncbi.nlm.nih.gov/pubmed/33583913
http://dx.doi.org/10.1292/jvms.20-0435
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author ABOU MONSEF, Yanad
KUTSAL, Osman
author_facet ABOU MONSEF, Yanad
KUTSAL, Osman
author_sort ABOU MONSEF, Yanad
collection PubMed
description Hepatic progenitor cells are periportally resident cells capable of differentiating into mature hepatocytes or cholangiocytes to ensure hepatic regeneration. This reaction is termed a ductular reaction. In the present study, regenerative response of the feline liver to different hepatic diseases was investigated immunohistochemically. Regeneration of the liver through hepatocellular replication and proliferation of progenitor cell compartment were comparatively evaluated. Histological and immunohistochemical stainings were conducted on feline liver samples (n=40) representing various hepatobiliary diseases. Cytokeratin (CK) 7, CK19, Proliferating cell nuclear antigen (PCNA), Ki67, and Human hepatocyte marker 1 (Hep Par-1) were used. The presence of progenitor cells within feline livers was proved, both as passive cells in normal liver and as active cells (ductular reaction) in hepatic lesions. CK7 was found to be a suitable antibody for immunohistochemically detecting feline progenitor cells. In acute events, regeneration was predominantly shaped by the division of hepatocytes. In chronic events and severe acute events, hepatocytes lost their ability to divide and regeneration mainly occurred through progenitor cells. Location of the ductular reaction varied between different hepatic diseases. Parenchymal ductular reaction was detected in fulminant hepatitis, chronic hepatitis, hepatocellular lipidosis and metastatic lymphoma, whereas septal ductular reaction was detected in chronic hepatitis and metastatic lymphoma. Ductular reaction exhibited positive staining for Hep Par-1 in chronic and severe acute events. This study indicates the major role played by hepatic progenitor cells in regeneration of the feline liver. Moreover, it shows how the activation pattern of ductular reaction varies according to the hepatobiliary disease type.
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spelling pubmed-81113362021-05-13 Immunohistochemical evaluation of hepatic progenitor cells in different types of feline liver diseases ABOU MONSEF, Yanad KUTSAL, Osman J Vet Med Sci Pathology Hepatic progenitor cells are periportally resident cells capable of differentiating into mature hepatocytes or cholangiocytes to ensure hepatic regeneration. This reaction is termed a ductular reaction. In the present study, regenerative response of the feline liver to different hepatic diseases was investigated immunohistochemically. Regeneration of the liver through hepatocellular replication and proliferation of progenitor cell compartment were comparatively evaluated. Histological and immunohistochemical stainings were conducted on feline liver samples (n=40) representing various hepatobiliary diseases. Cytokeratin (CK) 7, CK19, Proliferating cell nuclear antigen (PCNA), Ki67, and Human hepatocyte marker 1 (Hep Par-1) were used. The presence of progenitor cells within feline livers was proved, both as passive cells in normal liver and as active cells (ductular reaction) in hepatic lesions. CK7 was found to be a suitable antibody for immunohistochemically detecting feline progenitor cells. In acute events, regeneration was predominantly shaped by the division of hepatocytes. In chronic events and severe acute events, hepatocytes lost their ability to divide and regeneration mainly occurred through progenitor cells. Location of the ductular reaction varied between different hepatic diseases. Parenchymal ductular reaction was detected in fulminant hepatitis, chronic hepatitis, hepatocellular lipidosis and metastatic lymphoma, whereas septal ductular reaction was detected in chronic hepatitis and metastatic lymphoma. Ductular reaction exhibited positive staining for Hep Par-1 in chronic and severe acute events. This study indicates the major role played by hepatic progenitor cells in regeneration of the feline liver. Moreover, it shows how the activation pattern of ductular reaction varies according to the hepatobiliary disease type. The Japanese Society of Veterinary Science 2021-02-11 2021-04 /pmc/articles/PMC8111336/ /pubmed/33583913 http://dx.doi.org/10.1292/jvms.20-0435 Text en ©2021 The Japanese Society of Veterinary Science https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. (CC-BY-NC-ND 4.0: https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Pathology
ABOU MONSEF, Yanad
KUTSAL, Osman
Immunohistochemical evaluation of hepatic progenitor cells in different types of feline liver diseases
title Immunohistochemical evaluation of hepatic progenitor cells in different types of feline liver diseases
title_full Immunohistochemical evaluation of hepatic progenitor cells in different types of feline liver diseases
title_fullStr Immunohistochemical evaluation of hepatic progenitor cells in different types of feline liver diseases
title_full_unstemmed Immunohistochemical evaluation of hepatic progenitor cells in different types of feline liver diseases
title_short Immunohistochemical evaluation of hepatic progenitor cells in different types of feline liver diseases
title_sort immunohistochemical evaluation of hepatic progenitor cells in different types of feline liver diseases
topic Pathology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8111336/
https://www.ncbi.nlm.nih.gov/pubmed/33583913
http://dx.doi.org/10.1292/jvms.20-0435
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