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Distinct EpCAM-Positive Stem Cell Niches Are Engaged in Chronic and Neoplastic Liver Diseases
In normal human livers, EpCAM(pos) cells are mostly restricted in two distinct niches, which are (i) the bile ductules and (ii) the mucous glands present inside the wall of large intrahepatic bile ducts (the so-called peribiliary glands). These EpCAM(pos) cell niches have been proven to harbor stem/...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7492539/ https://www.ncbi.nlm.nih.gov/pubmed/32984373 http://dx.doi.org/10.3389/fmed.2020.00479 |
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author | Safarikia, Samira Carpino, Guido Overi, Diletta Cardinale, Vincenzo Venere, Rosanna Franchitto, Antonio Onori, Paolo Alvaro, Domenico Gaudio, Eugenio |
author_facet | Safarikia, Samira Carpino, Guido Overi, Diletta Cardinale, Vincenzo Venere, Rosanna Franchitto, Antonio Onori, Paolo Alvaro, Domenico Gaudio, Eugenio |
author_sort | Safarikia, Samira |
collection | PubMed |
description | In normal human livers, EpCAM(pos) cells are mostly restricted in two distinct niches, which are (i) the bile ductules and (ii) the mucous glands present inside the wall of large intrahepatic bile ducts (the so-called peribiliary glands). These EpCAM(pos) cell niches have been proven to harbor stem/progenitor cells with great importance in liver and biliary tree regeneration and in the pathophysiology of human diseases. The EpCAM(pos) progenitor cells within bile ductules are engaged in driving regenerative processes in chronic diseases affecting hepatocytes or interlobular bile ducts. The EpCAM(pos) population within peribiliary glands is activated when regenerative needs are finalized to repair large intra- or extra-hepatic bile ducts affected by chronic pathologies, including primary sclerosing cholangitis and ischemia-induced cholangiopathies after orthotopic liver transplantation. Finally, the presence of distinct EpCAM(pos) cell populations may explain the histological and molecular heterogeneity characterizing cholangiocarcinoma, based on the concept of multiple candidate cells of origin. This review aimed to describe the precise anatomical distribution of EpCAM(pos) populations within the liver and the biliary tree and to discuss their contribution in the pathophysiology of human liver diseases, as well as their potential role in regenerative medicine of the liver. |
format | Online Article Text |
id | pubmed-7492539 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74925392020-09-25 Distinct EpCAM-Positive Stem Cell Niches Are Engaged in Chronic and Neoplastic Liver Diseases Safarikia, Samira Carpino, Guido Overi, Diletta Cardinale, Vincenzo Venere, Rosanna Franchitto, Antonio Onori, Paolo Alvaro, Domenico Gaudio, Eugenio Front Med (Lausanne) Medicine In normal human livers, EpCAM(pos) cells are mostly restricted in two distinct niches, which are (i) the bile ductules and (ii) the mucous glands present inside the wall of large intrahepatic bile ducts (the so-called peribiliary glands). These EpCAM(pos) cell niches have been proven to harbor stem/progenitor cells with great importance in liver and biliary tree regeneration and in the pathophysiology of human diseases. The EpCAM(pos) progenitor cells within bile ductules are engaged in driving regenerative processes in chronic diseases affecting hepatocytes or interlobular bile ducts. The EpCAM(pos) population within peribiliary glands is activated when regenerative needs are finalized to repair large intra- or extra-hepatic bile ducts affected by chronic pathologies, including primary sclerosing cholangitis and ischemia-induced cholangiopathies after orthotopic liver transplantation. Finally, the presence of distinct EpCAM(pos) cell populations may explain the histological and molecular heterogeneity characterizing cholangiocarcinoma, based on the concept of multiple candidate cells of origin. This review aimed to describe the precise anatomical distribution of EpCAM(pos) populations within the liver and the biliary tree and to discuss their contribution in the pathophysiology of human liver diseases, as well as their potential role in regenerative medicine of the liver. Frontiers Media S.A. 2020-09-02 /pmc/articles/PMC7492539/ /pubmed/32984373 http://dx.doi.org/10.3389/fmed.2020.00479 Text en Copyright © 2020 Safarikia, Carpino, Overi, Cardinale, Venere, Franchitto, Onori, Alvaro and Gaudio. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Medicine Safarikia, Samira Carpino, Guido Overi, Diletta Cardinale, Vincenzo Venere, Rosanna Franchitto, Antonio Onori, Paolo Alvaro, Domenico Gaudio, Eugenio Distinct EpCAM-Positive Stem Cell Niches Are Engaged in Chronic and Neoplastic Liver Diseases |
title | Distinct EpCAM-Positive Stem Cell Niches Are Engaged in Chronic and Neoplastic Liver Diseases |
title_full | Distinct EpCAM-Positive Stem Cell Niches Are Engaged in Chronic and Neoplastic Liver Diseases |
title_fullStr | Distinct EpCAM-Positive Stem Cell Niches Are Engaged in Chronic and Neoplastic Liver Diseases |
title_full_unstemmed | Distinct EpCAM-Positive Stem Cell Niches Are Engaged in Chronic and Neoplastic Liver Diseases |
title_short | Distinct EpCAM-Positive Stem Cell Niches Are Engaged in Chronic and Neoplastic Liver Diseases |
title_sort | distinct epcam-positive stem cell niches are engaged in chronic and neoplastic liver diseases |
topic | Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7492539/ https://www.ncbi.nlm.nih.gov/pubmed/32984373 http://dx.doi.org/10.3389/fmed.2020.00479 |
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