Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Mészáros, Beáta, Papp, Ferenc, Mocsár, Gábor, Kókai, Endre, Kovács, Katalin, Tajti, Gabor, Panyi, Gyorgy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
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
_version_ 1783527381708832768
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
work_keys_str_mv AT meszarosbeata thevoltagegatedprotonchannelhhv1isfunctionallyexpressedinhumanchorionderivedmesenchymalstemcells
AT pappferenc thevoltagegatedprotonchannelhhv1isfunctionallyexpressedinhumanchorionderivedmesenchymalstemcells
AT mocsargabor thevoltagegatedprotonchannelhhv1isfunctionallyexpressedinhumanchorionderivedmesenchymalstemcells
AT kokaiendre thevoltagegatedprotonchannelhhv1isfunctionallyexpressedinhumanchorionderivedmesenchymalstemcells
AT kovacskatalin thevoltagegatedprotonchannelhhv1isfunctionallyexpressedinhumanchorionderivedmesenchymalstemcells
AT tajtigabor thevoltagegatedprotonchannelhhv1isfunctionallyexpressedinhumanchorionderivedmesenchymalstemcells
AT panyigyorgy thevoltagegatedprotonchannelhhv1isfunctionallyexpressedinhumanchorionderivedmesenchymalstemcells
AT meszarosbeata voltagegatedprotonchannelhhv1isfunctionallyexpressedinhumanchorionderivedmesenchymalstemcells
AT pappferenc voltagegatedprotonchannelhhv1isfunctionallyexpressedinhumanchorionderivedmesenchymalstemcells
AT mocsargabor voltagegatedprotonchannelhhv1isfunctionallyexpressedinhumanchorionderivedmesenchymalstemcells
AT kokaiendre voltagegatedprotonchannelhhv1isfunctionallyexpressedinhumanchorionderivedmesenchymalstemcells
AT kovacskatalin voltagegatedprotonchannelhhv1isfunctionallyexpressedinhumanchorionderivedmesenchymalstemcells
AT tajtigabor voltagegatedprotonchannelhhv1isfunctionallyexpressedinhumanchorionderivedmesenchymalstemcells
AT panyigyorgy voltagegatedprotonchannelhhv1isfunctionallyexpressedinhumanchorionderivedmesenchymalstemcells