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Hepatic progenitors for liver disease: current position
Liver regeneration restores the original functionality of hepatocytes and cholangiocytes in response to injury. It is regulated on several levels, with different cellular populations contributing to this process, eg, hepatocytes, liver precursor cells, intrahepatic stem cells. In response to injury,...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3781731/ https://www.ncbi.nlm.nih.gov/pubmed/24198509 |
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author | Conigliaro, Alice Brenner, David A Kisseleva, Tatiana |
author_facet | Conigliaro, Alice Brenner, David A Kisseleva, Tatiana |
author_sort | Conigliaro, Alice |
collection | PubMed |
description | Liver regeneration restores the original functionality of hepatocytes and cholangiocytes in response to injury. It is regulated on several levels, with different cellular populations contributing to this process, eg, hepatocytes, liver precursor cells, intrahepatic stem cells. In response to injury, mature hepatocytes have the capability to proliferate and give rise to new hepatocytes and cholangiocytes. Meanwhile, liver precursor cells (oval cells) have become the most recognized bipotential precursor cells in the damaged liver. They rapidly proliferate, change their cellular composition, and differentiate into hepatocytes and cholangiocytes to compensate for the cellular loss and maintain liver homeostasis. There is a growing body of evidence that oval cells originate from the intrahepatic stem cell(s), which in turn give(s) rise to epithelial, including oval cells, and/or other hepatic cells of nonepithelial origin. Since there is a close relationship between the liver and hematopoiesis, bone marrow derived cells can also contribute to liver regeneration by the fusion of myeloid cells with damaged hepatocytes, or differentiation of mesenchymal stem cells into hepatocyte-like cells. The current review discusses the contribution of different cells to liver regeneration and their characteristics. |
format | Online Article Text |
id | pubmed-3781731 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-37817312013-11-06 Hepatic progenitors for liver disease: current position Conigliaro, Alice Brenner, David A Kisseleva, Tatiana Stem Cells Cloning Review Liver regeneration restores the original functionality of hepatocytes and cholangiocytes in response to injury. It is regulated on several levels, with different cellular populations contributing to this process, eg, hepatocytes, liver precursor cells, intrahepatic stem cells. In response to injury, mature hepatocytes have the capability to proliferate and give rise to new hepatocytes and cholangiocytes. Meanwhile, liver precursor cells (oval cells) have become the most recognized bipotential precursor cells in the damaged liver. They rapidly proliferate, change their cellular composition, and differentiate into hepatocytes and cholangiocytes to compensate for the cellular loss and maintain liver homeostasis. There is a growing body of evidence that oval cells originate from the intrahepatic stem cell(s), which in turn give(s) rise to epithelial, including oval cells, and/or other hepatic cells of nonepithelial origin. Since there is a close relationship between the liver and hematopoiesis, bone marrow derived cells can also contribute to liver regeneration by the fusion of myeloid cells with damaged hepatocytes, or differentiation of mesenchymal stem cells into hepatocyte-like cells. The current review discusses the contribution of different cells to liver regeneration and their characteristics. Dove Medical Press 2010-02-25 /pmc/articles/PMC3781731/ /pubmed/24198509 Text en © 2010 Conigliaro et al, publisher and licensee Dove Medical Press Ltd This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited. |
spellingShingle | Review Conigliaro, Alice Brenner, David A Kisseleva, Tatiana Hepatic progenitors for liver disease: current position |
title | Hepatic progenitors for liver disease: current position |
title_full | Hepatic progenitors for liver disease: current position |
title_fullStr | Hepatic progenitors for liver disease: current position |
title_full_unstemmed | Hepatic progenitors for liver disease: current position |
title_short | Hepatic progenitors for liver disease: current position |
title_sort | hepatic progenitors for liver disease: current position |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3781731/ https://www.ncbi.nlm.nih.gov/pubmed/24198509 |
work_keys_str_mv | AT conigliaroalice hepaticprogenitorsforliverdiseasecurrentposition AT brennerdavida hepaticprogenitorsforliverdiseasecurrentposition AT kisselevatatiana hepaticprogenitorsforliverdiseasecurrentposition |