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Functional diversity of TMPRSS6 isoforms and variants expressed in hepatocellular carcinoma cell lines
TMPRSS6, also known as matriptase-2, is a type II transmembrane serine protease that plays a major role in iron homeostasis by acting as a negative regulator of hepcidin production through cleavage of the BMP co-receptor haemojuvelin. Iron-refractory iron deficiency anaemia (IRIDA), an iron metaboli...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6105633/ https://www.ncbi.nlm.nih.gov/pubmed/30135444 http://dx.doi.org/10.1038/s41598-018-30618-z |
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author | Dion, Sébastien P. Béliveau, François Morency, Louis-Philippe Désilets, Antoine Najmanovich, Rafaël Leduc, Richard |
author_facet | Dion, Sébastien P. Béliveau, François Morency, Louis-Philippe Désilets, Antoine Najmanovich, Rafaël Leduc, Richard |
author_sort | Dion, Sébastien P. |
collection | PubMed |
description | TMPRSS6, also known as matriptase-2, is a type II transmembrane serine protease that plays a major role in iron homeostasis by acting as a negative regulator of hepcidin production through cleavage of the BMP co-receptor haemojuvelin. Iron-refractory iron deficiency anaemia (IRIDA), an iron metabolism disorder, is associated with mutations in the TMPRSS6 gene. By analysing RNA-seq data encoding TMPRSS6 isoforms and other proteins involved in hepcidin production, we uncovered significant differences in expression levels between hepatocellular carcinoma (HCC) cell lines and normal human liver samples. Most notably, TMPRSS6 and HAMP expression was found to be much lower in HepG2 and Huh7 cells when compared to human liver samples. Furthermore, we characterized the common TMPRSS6 polymorphism V736A identified in Hep3B cells, the V795I mutation found in HepG2 cells, also associated with IRIDA, and the G603R substitution recently detected in two IRIDA patients. While variant V736A is as active as wild-type TMPRSS6, mutants V795I and G603R displayed significantly reduced proteolytic activity. Our results provide important information about commonly used liver cell models and shed light on the impact of two TMPRSS6 mutations associated with IRIDA. |
format | Online Article Text |
id | pubmed-6105633 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61056332018-08-27 Functional diversity of TMPRSS6 isoforms and variants expressed in hepatocellular carcinoma cell lines Dion, Sébastien P. Béliveau, François Morency, Louis-Philippe Désilets, Antoine Najmanovich, Rafaël Leduc, Richard Sci Rep Article TMPRSS6, also known as matriptase-2, is a type II transmembrane serine protease that plays a major role in iron homeostasis by acting as a negative regulator of hepcidin production through cleavage of the BMP co-receptor haemojuvelin. Iron-refractory iron deficiency anaemia (IRIDA), an iron metabolism disorder, is associated with mutations in the TMPRSS6 gene. By analysing RNA-seq data encoding TMPRSS6 isoforms and other proteins involved in hepcidin production, we uncovered significant differences in expression levels between hepatocellular carcinoma (HCC) cell lines and normal human liver samples. Most notably, TMPRSS6 and HAMP expression was found to be much lower in HepG2 and Huh7 cells when compared to human liver samples. Furthermore, we characterized the common TMPRSS6 polymorphism V736A identified in Hep3B cells, the V795I mutation found in HepG2 cells, also associated with IRIDA, and the G603R substitution recently detected in two IRIDA patients. While variant V736A is as active as wild-type TMPRSS6, mutants V795I and G603R displayed significantly reduced proteolytic activity. Our results provide important information about commonly used liver cell models and shed light on the impact of two TMPRSS6 mutations associated with IRIDA. Nature Publishing Group UK 2018-08-22 /pmc/articles/PMC6105633/ /pubmed/30135444 http://dx.doi.org/10.1038/s41598-018-30618-z Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Dion, Sébastien P. Béliveau, François Morency, Louis-Philippe Désilets, Antoine Najmanovich, Rafaël Leduc, Richard Functional diversity of TMPRSS6 isoforms and variants expressed in hepatocellular carcinoma cell lines |
title | Functional diversity of TMPRSS6 isoforms and variants expressed in hepatocellular carcinoma cell lines |
title_full | Functional diversity of TMPRSS6 isoforms and variants expressed in hepatocellular carcinoma cell lines |
title_fullStr | Functional diversity of TMPRSS6 isoforms and variants expressed in hepatocellular carcinoma cell lines |
title_full_unstemmed | Functional diversity of TMPRSS6 isoforms and variants expressed in hepatocellular carcinoma cell lines |
title_short | Functional diversity of TMPRSS6 isoforms and variants expressed in hepatocellular carcinoma cell lines |
title_sort | functional diversity of tmprss6 isoforms and variants expressed in hepatocellular carcinoma cell lines |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6105633/ https://www.ncbi.nlm.nih.gov/pubmed/30135444 http://dx.doi.org/10.1038/s41598-018-30618-z |
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