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Maintaining Hepatic Stem Cell Gene Expression on Biological and Synthetic Substrata

The liver is a highly resilient organ that possesses enormous regenerative capacity. This is mediated mainly through the most abundant cell type found in the liver, the hepatocyte. When the regenerative capacity of the hepatocyte is compromised, during chronic or acute liver injury, hepatic progenit...

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Autores principales: Lucendo-Villarin, Baltasar, Khan, Ferdous, Pernagallo, Salvatore, Bradley, Mark, Iredale, John P., Hay, David C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mary Ann Liebert, Inc. 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3559223/
https://www.ncbi.nlm.nih.gov/pubmed/23515003
http://dx.doi.org/10.1089/biores.2012.0206
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author Lucendo-Villarin, Baltasar
Khan, Ferdous
Pernagallo, Salvatore
Bradley, Mark
Iredale, John P.
Hay, David C.
author_facet Lucendo-Villarin, Baltasar
Khan, Ferdous
Pernagallo, Salvatore
Bradley, Mark
Iredale, John P.
Hay, David C.
author_sort Lucendo-Villarin, Baltasar
collection PubMed
description The liver is a highly resilient organ that possesses enormous regenerative capacity. This is mediated mainly through the most abundant cell type found in the liver, the hepatocyte. When the regenerative capacity of the hepatocyte is compromised, during chronic or acute liver injury, hepatic progenitor cells (HPCs) are activated to replace the damaged tissue. The HPC resides in a laminin-rich environment; as HPCs differentiate toward a hepatic or biliary fate, the extracellular matrix (ECM) composition changes, influencing cell behavior. To assess the impact that the biological ECM and the synthetic ECM have on the maintenance of hepatic stem cell gene expression, a murine hepatic stem cell line was employed. We demonstrate that hepatic stem cell gene expression could be maintained using a biological or synthetic substratum, but not on plastic alone.
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spelling pubmed-35592232013-03-20 Maintaining Hepatic Stem Cell Gene Expression on Biological and Synthetic Substrata Lucendo-Villarin, Baltasar Khan, Ferdous Pernagallo, Salvatore Bradley, Mark Iredale, John P. Hay, David C. Biores Open Access Brief Report The liver is a highly resilient organ that possesses enormous regenerative capacity. This is mediated mainly through the most abundant cell type found in the liver, the hepatocyte. When the regenerative capacity of the hepatocyte is compromised, during chronic or acute liver injury, hepatic progenitor cells (HPCs) are activated to replace the damaged tissue. The HPC resides in a laminin-rich environment; as HPCs differentiate toward a hepatic or biliary fate, the extracellular matrix (ECM) composition changes, influencing cell behavior. To assess the impact that the biological ECM and the synthetic ECM have on the maintenance of hepatic stem cell gene expression, a murine hepatic stem cell line was employed. We demonstrate that hepatic stem cell gene expression could be maintained using a biological or synthetic substratum, but not on plastic alone. Mary Ann Liebert, Inc. 2012-01 /pmc/articles/PMC3559223/ /pubmed/23515003 http://dx.doi.org/10.1089/biores.2012.0206 Text en Copyright 2012, Mary Ann Liebert, Inc.
spellingShingle Brief Report
Lucendo-Villarin, Baltasar
Khan, Ferdous
Pernagallo, Salvatore
Bradley, Mark
Iredale, John P.
Hay, David C.
Maintaining Hepatic Stem Cell Gene Expression on Biological and Synthetic Substrata
title Maintaining Hepatic Stem Cell Gene Expression on Biological and Synthetic Substrata
title_full Maintaining Hepatic Stem Cell Gene Expression on Biological and Synthetic Substrata
title_fullStr Maintaining Hepatic Stem Cell Gene Expression on Biological and Synthetic Substrata
title_full_unstemmed Maintaining Hepatic Stem Cell Gene Expression on Biological and Synthetic Substrata
title_short Maintaining Hepatic Stem Cell Gene Expression on Biological and Synthetic Substrata
title_sort maintaining hepatic stem cell gene expression on biological and synthetic substrata
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3559223/
https://www.ncbi.nlm.nih.gov/pubmed/23515003
http://dx.doi.org/10.1089/biores.2012.0206
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