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Hepcidin is potential regulator for renin activity
An association between genetic variants in the genes HFE, HJV, BMP4 and arterial hypertension has been shown earlier. Proteins encoded by these genes participate in the signalling routes leading eventually to the production of the peptide hormone hepcidin. Mutations in these genes have been associat...
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/PMC9020709/ https://www.ncbi.nlm.nih.gov/pubmed/35442992 http://dx.doi.org/10.1371/journal.pone.0267343 |
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author | Piesanen, Jaakko Valjakka, Jarkko Niemelä, Sanna Borgenström, Marjut Nikkari, Seppo Hytönen, Vesa Määttä, Juha Kunnas, Tarja |
author_facet | Piesanen, Jaakko Valjakka, Jarkko Niemelä, Sanna Borgenström, Marjut Nikkari, Seppo Hytönen, Vesa Määttä, Juha Kunnas, Tarja |
author_sort | Piesanen, Jaakko |
collection | PubMed |
description | An association between genetic variants in the genes HFE, HJV, BMP4 and arterial hypertension has been shown earlier. Proteins encoded by these genes participate in the signalling routes leading eventually to the production of the peptide hormone hepcidin. Mutations in these genes have been associated with the abnormal production of hepcidin in the body. This finding led to studies exploring the possible role of hepcidin in regulating the activity of blood pressure related renin-angiotensin system enzymes. We used molecular modelling to find out if it is possible for hepcidin to bind to the active site of the renin-angiotensin system enzymes, especially renin. Fluorometric assays were used to evaluate the inhibitory effect of hepcidin on renin as well as angiotensin converting enzymes 1 and 2. Finally, bio-layer interferometry technique was used to study hepcidin binding to renin. The molecular modelling showed that hepcidin seems to have similar binding properties to the renin active site as angiotensinogen does. Based on fluorometric enzyme activity assay, hepcidin has an inhibitory effect on renin in vitro, too. However, angiotensin converting enzymes 1 and 2 were not inhibited remarkably by hepcidin-25. In bio-layer interferometry analysis hepcidin-renin binding was concentration dependent. Our results suggest that hepcidin could act as an inhibitor to the renin. Nowadays, there is no known biological inhibitor for renin in vivo and our finding may thus have important clinical implications. |
format | Online Article Text |
id | pubmed-9020709 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-90207092022-04-21 Hepcidin is potential regulator for renin activity Piesanen, Jaakko Valjakka, Jarkko Niemelä, Sanna Borgenström, Marjut Nikkari, Seppo Hytönen, Vesa Määttä, Juha Kunnas, Tarja PLoS One Research Article An association between genetic variants in the genes HFE, HJV, BMP4 and arterial hypertension has been shown earlier. Proteins encoded by these genes participate in the signalling routes leading eventually to the production of the peptide hormone hepcidin. Mutations in these genes have been associated with the abnormal production of hepcidin in the body. This finding led to studies exploring the possible role of hepcidin in regulating the activity of blood pressure related renin-angiotensin system enzymes. We used molecular modelling to find out if it is possible for hepcidin to bind to the active site of the renin-angiotensin system enzymes, especially renin. Fluorometric assays were used to evaluate the inhibitory effect of hepcidin on renin as well as angiotensin converting enzymes 1 and 2. Finally, bio-layer interferometry technique was used to study hepcidin binding to renin. The molecular modelling showed that hepcidin seems to have similar binding properties to the renin active site as angiotensinogen does. Based on fluorometric enzyme activity assay, hepcidin has an inhibitory effect on renin in vitro, too. However, angiotensin converting enzymes 1 and 2 were not inhibited remarkably by hepcidin-25. In bio-layer interferometry analysis hepcidin-renin binding was concentration dependent. Our results suggest that hepcidin could act as an inhibitor to the renin. Nowadays, there is no known biological inhibitor for renin in vivo and our finding may thus have important clinical implications. Public Library of Science 2022-04-20 /pmc/articles/PMC9020709/ /pubmed/35442992 http://dx.doi.org/10.1371/journal.pone.0267343 Text en © 2022 Piesanen 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 Piesanen, Jaakko Valjakka, Jarkko Niemelä, Sanna Borgenström, Marjut Nikkari, Seppo Hytönen, Vesa Määttä, Juha Kunnas, Tarja Hepcidin is potential regulator for renin activity |
title | Hepcidin is potential regulator for renin activity |
title_full | Hepcidin is potential regulator for renin activity |
title_fullStr | Hepcidin is potential regulator for renin activity |
title_full_unstemmed | Hepcidin is potential regulator for renin activity |
title_short | Hepcidin is potential regulator for renin activity |
title_sort | hepcidin is potential regulator for renin activity |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9020709/ https://www.ncbi.nlm.nih.gov/pubmed/35442992 http://dx.doi.org/10.1371/journal.pone.0267343 |
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