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Glioblastoma cancer stem cell lines express functional acid sensing ion channels ASIC1a and ASIC3
Acidic microenvironment is commonly observed in tumour tissues, including glioblastoma (GBM), the most aggressive and lethal brain tumour in adults. Acid sensing ion channels (ASICs) are neuronal voltage-insensitive sodium channels, which are sensors of extracellular protons. Here we studied and fun...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5651884/ https://www.ncbi.nlm.nih.gov/pubmed/29057936 http://dx.doi.org/10.1038/s41598-017-13666-9 |
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author | Tian, Yuemin Bresenitz, Pia Reska, Anna El Moussaoui, Laila Beier, Christoph Patrick Gründer, Stefan |
author_facet | Tian, Yuemin Bresenitz, Pia Reska, Anna El Moussaoui, Laila Beier, Christoph Patrick Gründer, Stefan |
author_sort | Tian, Yuemin |
collection | PubMed |
description | Acidic microenvironment is commonly observed in tumour tissues, including glioblastoma (GBM), the most aggressive and lethal brain tumour in adults. Acid sensing ion channels (ASICs) are neuronal voltage-insensitive sodium channels, which are sensors of extracellular protons. Here we studied and functionally characterized ASICs in two primary glioblastoma stem cell lines as cell culture models. We detected transcripts of the ACCN2 and ACCN3 genes, coding for ASIC1 and ASIC3, respectively, but not transcripts of ACCN1 (coding for ASIC2). Available microarray data confirmed that ACCN1 is downregulated in glioma. Western blotting confirmed expression of ASIC1 and ASIC3, the most proton-sensitive ASICs, in both GBM cell lines. We characterized ASICs functionally using whole-cell patch clamp and detected different types of acid-sensitive currents. Some of these currents had kinetics typical for ASICs and were sensitive to specific toxin inhibitors of ASIC1a or ASIC3, demonstrating that the GBM cell lines express functional ASIC1a and ASIC3 that may enable GBM cells to sensitively detect extracellular pH in a tumour tissue. Microarray data revealed that expression of ACCN2 and ACCN3 is associated with improved survival of patients suffering from gliomas, suggesting that preserved susceptibility to extracellular pH may impair tumour growth. |
format | Online Article Text |
id | pubmed-5651884 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56518842017-10-26 Glioblastoma cancer stem cell lines express functional acid sensing ion channels ASIC1a and ASIC3 Tian, Yuemin Bresenitz, Pia Reska, Anna El Moussaoui, Laila Beier, Christoph Patrick Gründer, Stefan Sci Rep Article Acidic microenvironment is commonly observed in tumour tissues, including glioblastoma (GBM), the most aggressive and lethal brain tumour in adults. Acid sensing ion channels (ASICs) are neuronal voltage-insensitive sodium channels, which are sensors of extracellular protons. Here we studied and functionally characterized ASICs in two primary glioblastoma stem cell lines as cell culture models. We detected transcripts of the ACCN2 and ACCN3 genes, coding for ASIC1 and ASIC3, respectively, but not transcripts of ACCN1 (coding for ASIC2). Available microarray data confirmed that ACCN1 is downregulated in glioma. Western blotting confirmed expression of ASIC1 and ASIC3, the most proton-sensitive ASICs, in both GBM cell lines. We characterized ASICs functionally using whole-cell patch clamp and detected different types of acid-sensitive currents. Some of these currents had kinetics typical for ASICs and were sensitive to specific toxin inhibitors of ASIC1a or ASIC3, demonstrating that the GBM cell lines express functional ASIC1a and ASIC3 that may enable GBM cells to sensitively detect extracellular pH in a tumour tissue. Microarray data revealed that expression of ACCN2 and ACCN3 is associated with improved survival of patients suffering from gliomas, suggesting that preserved susceptibility to extracellular pH may impair tumour growth. Nature Publishing Group UK 2017-10-20 /pmc/articles/PMC5651884/ /pubmed/29057936 http://dx.doi.org/10.1038/s41598-017-13666-9 Text en © The Author(s) 2017 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 Tian, Yuemin Bresenitz, Pia Reska, Anna El Moussaoui, Laila Beier, Christoph Patrick Gründer, Stefan Glioblastoma cancer stem cell lines express functional acid sensing ion channels ASIC1a and ASIC3 |
title | Glioblastoma cancer stem cell lines express functional acid sensing ion channels ASIC1a and ASIC3 |
title_full | Glioblastoma cancer stem cell lines express functional acid sensing ion channels ASIC1a and ASIC3 |
title_fullStr | Glioblastoma cancer stem cell lines express functional acid sensing ion channels ASIC1a and ASIC3 |
title_full_unstemmed | Glioblastoma cancer stem cell lines express functional acid sensing ion channels ASIC1a and ASIC3 |
title_short | Glioblastoma cancer stem cell lines express functional acid sensing ion channels ASIC1a and ASIC3 |
title_sort | glioblastoma cancer stem cell lines express functional acid sensing ion channels asic1a and asic3 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5651884/ https://www.ncbi.nlm.nih.gov/pubmed/29057936 http://dx.doi.org/10.1038/s41598-017-13666-9 |
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