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Functionally impaired isoforms regulate TMPRSS6 proteolytic activity
TMPRSS6 is a type II transmembrane serine protease involved in iron homeostasis expressed as 4 isoforms in humans. TMPRSS6 isoform 2 downregulates hepcidin production by cleaving hemojuvelin and other surface proteins of hepatocytes. The functions of catalytically impaired isoforms 3 and 4 are still...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9432768/ https://www.ncbi.nlm.nih.gov/pubmed/36044454 http://dx.doi.org/10.1371/journal.pone.0273825 |
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author | Dion, Sébastien P. Désilets, Antoine Lemieux, Gabriel Leduc, Richard |
author_facet | Dion, Sébastien P. Désilets, Antoine Lemieux, Gabriel Leduc, Richard |
author_sort | Dion, Sébastien P. |
collection | PubMed |
description | TMPRSS6 is a type II transmembrane serine protease involved in iron homeostasis expressed as 4 isoforms in humans. TMPRSS6 isoform 2 downregulates hepcidin production by cleaving hemojuvelin and other surface proteins of hepatocytes. The functions of catalytically impaired isoforms 3 and 4 are still unknown. Here we demonstrate that TMPRSS6 isoforms 3 and 4 reduce the proteolytic activity of isoform 2 and uncover the ability of isoforms to interact. Moreover, we identified 49 potential protein partners common to TMPRSS6 isoforms, including TfR1, known to be involved in iron regulation. By co-expressing TMPRSS6 and TfR1, we show that TfR1 is cleaved and shed from the cell surface. Further, we demonstrate that TMPRSS6 isoforms 3 and 4 behave as dominant negative. |
format | Online Article Text |
id | pubmed-9432768 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-94327682022-09-01 Functionally impaired isoforms regulate TMPRSS6 proteolytic activity Dion, Sébastien P. Désilets, Antoine Lemieux, Gabriel Leduc, Richard PLoS One Research Article TMPRSS6 is a type II transmembrane serine protease involved in iron homeostasis expressed as 4 isoforms in humans. TMPRSS6 isoform 2 downregulates hepcidin production by cleaving hemojuvelin and other surface proteins of hepatocytes. The functions of catalytically impaired isoforms 3 and 4 are still unknown. Here we demonstrate that TMPRSS6 isoforms 3 and 4 reduce the proteolytic activity of isoform 2 and uncover the ability of isoforms to interact. Moreover, we identified 49 potential protein partners common to TMPRSS6 isoforms, including TfR1, known to be involved in iron regulation. By co-expressing TMPRSS6 and TfR1, we show that TfR1 is cleaved and shed from the cell surface. Further, we demonstrate that TMPRSS6 isoforms 3 and 4 behave as dominant negative. Public Library of Science 2022-08-31 /pmc/articles/PMC9432768/ /pubmed/36044454 http://dx.doi.org/10.1371/journal.pone.0273825 Text en © 2022 Dion et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Dion, Sébastien P. Désilets, Antoine Lemieux, Gabriel Leduc, Richard Functionally impaired isoforms regulate TMPRSS6 proteolytic activity |
title | Functionally impaired isoforms regulate TMPRSS6 proteolytic activity |
title_full | Functionally impaired isoforms regulate TMPRSS6 proteolytic activity |
title_fullStr | Functionally impaired isoforms regulate TMPRSS6 proteolytic activity |
title_full_unstemmed | Functionally impaired isoforms regulate TMPRSS6 proteolytic activity |
title_short | Functionally impaired isoforms regulate TMPRSS6 proteolytic activity |
title_sort | functionally impaired isoforms regulate tmprss6 proteolytic activity |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9432768/ https://www.ncbi.nlm.nih.gov/pubmed/36044454 http://dx.doi.org/10.1371/journal.pone.0273825 |
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