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The voltage-gated proton channel hHv1 is functionally expressed in human chorion-derived mesenchymal stem cells
The voltage-gated proton channel Hv1 is widely expressed, among others, in immune and cancer cells, it provides an efficient cytosolic H(+)extrusion mechanism and regulates vital functions such as oxidative burst, migration and proliferation. Here we demonstrate the presence of human Hv1 (hHv1) in t...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7188850/ https://www.ncbi.nlm.nih.gov/pubmed/32346069 http://dx.doi.org/10.1038/s41598-020-63517-3 |
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author | Mészáros, Beáta Papp, Ferenc Mocsár, Gábor Kókai, Endre Kovács, Katalin Tajti, Gabor Panyi, Gyorgy |
author_facet | Mészáros, Beáta Papp, Ferenc Mocsár, Gábor Kókai, Endre Kovács, Katalin Tajti, Gabor Panyi, Gyorgy |
author_sort | Mészáros, Beáta |
collection | PubMed |
description | The voltage-gated proton channel Hv1 is widely expressed, among others, in immune and cancer cells, it provides an efficient cytosolic H(+)extrusion mechanism and regulates vital functions such as oxidative burst, migration and proliferation. Here we demonstrate the presence of human Hv1 (hHv1) in the placenta/chorion-derived mesenchymal stem cells (cMSCs) using RT-PCR. The voltage- and pH-dependent gating of the current is similar to that of hHv1 expressed in cell lines and that the current is blocked by 5-chloro-2-guanidinobenzimidazole (ClGBI) and activated by arachidonic acid (AA). Inhibition of hHv1 by ClGBI significantly decreases mineral matrix production of cMSCs induced by conditions mimicking physiological or pathological (inorganic phosphate, Pi) induction of osteogenesis. Wound healing assay and single cell motility analysis show that ClGBI significantly inhibits the migration of cMSCs. Thus, seminal functions of cMSCs are modulated by hHv1 which makes this channel as an attractive target for controlling advantages/disadvantages of MSCs therapy. |
format | Online Article Text |
id | pubmed-7188850 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-71888502020-05-04 The voltage-gated proton channel hHv1 is functionally expressed in human chorion-derived mesenchymal stem cells Mészáros, Beáta Papp, Ferenc Mocsár, Gábor Kókai, Endre Kovács, Katalin Tajti, Gabor Panyi, Gyorgy Sci Rep Article The voltage-gated proton channel Hv1 is widely expressed, among others, in immune and cancer cells, it provides an efficient cytosolic H(+)extrusion mechanism and regulates vital functions such as oxidative burst, migration and proliferation. Here we demonstrate the presence of human Hv1 (hHv1) in the placenta/chorion-derived mesenchymal stem cells (cMSCs) using RT-PCR. The voltage- and pH-dependent gating of the current is similar to that of hHv1 expressed in cell lines and that the current is blocked by 5-chloro-2-guanidinobenzimidazole (ClGBI) and activated by arachidonic acid (AA). Inhibition of hHv1 by ClGBI significantly decreases mineral matrix production of cMSCs induced by conditions mimicking physiological or pathological (inorganic phosphate, Pi) induction of osteogenesis. Wound healing assay and single cell motility analysis show that ClGBI significantly inhibits the migration of cMSCs. Thus, seminal functions of cMSCs are modulated by hHv1 which makes this channel as an attractive target for controlling advantages/disadvantages of MSCs therapy. Nature Publishing Group UK 2020-04-28 /pmc/articles/PMC7188850/ /pubmed/32346069 http://dx.doi.org/10.1038/s41598-020-63517-3 Text en © The Author(s) 2020 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 Mészáros, Beáta Papp, Ferenc Mocsár, Gábor Kókai, Endre Kovács, Katalin Tajti, Gabor Panyi, Gyorgy The voltage-gated proton channel hHv1 is functionally expressed in human chorion-derived mesenchymal stem cells |
title | The voltage-gated proton channel hHv1 is functionally expressed in human chorion-derived mesenchymal stem cells |
title_full | The voltage-gated proton channel hHv1 is functionally expressed in human chorion-derived mesenchymal stem cells |
title_fullStr | The voltage-gated proton channel hHv1 is functionally expressed in human chorion-derived mesenchymal stem cells |
title_full_unstemmed | The voltage-gated proton channel hHv1 is functionally expressed in human chorion-derived mesenchymal stem cells |
title_short | The voltage-gated proton channel hHv1 is functionally expressed in human chorion-derived mesenchymal stem cells |
title_sort | voltage-gated proton channel hhv1 is functionally expressed in human chorion-derived mesenchymal stem cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7188850/ https://www.ncbi.nlm.nih.gov/pubmed/32346069 http://dx.doi.org/10.1038/s41598-020-63517-3 |
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