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Tannic acid inhibits electrogenic Na+/HCO3− co-transporter activity in embryonic neural stem cell-derived radial glial-like cells
Self-renewing neural stem cells and progenitor cells are cell populations that generate radial glial cells and neurons through asymmetric division. Regulation of intracellular pH in stem cells with high metabolic activity is critical for both cell signaling and proliferation. We have recently found...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6903378/ https://www.ncbi.nlm.nih.gov/pubmed/31714480 http://dx.doi.org/10.1097/WNR.0000000000001372 |
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author | Nordström, Tommy Zhenyu, Gao Andersson, Leif C. Åkerman, Karl E.O. |
author_facet | Nordström, Tommy Zhenyu, Gao Andersson, Leif C. Åkerman, Karl E.O. |
author_sort | Nordström, Tommy |
collection | PubMed |
description | Self-renewing neural stem cells and progenitor cells are cell populations that generate radial glial cells and neurons through asymmetric division. Regulation of intracellular pH in stem cells with high metabolic activity is critical for both cell signaling and proliferation. We have recently found that a S0859-inhibitable electrogenic Na(+)/HCO(3)(−) co-transporter (NBCe1, Slc4a4), is the primary pH(i) regulatory mechanism in stem cell-derived radial glial-like cells. Here we show, by using the voltage-sensitive fluorescent dye DiBAC(4)(3) and BCECF, a pH-sensitive dye, that an antioxidant, tannic acid (100 µM), can inhibit potassium- and calcium-dependent rapid changes in membrane potential and NBCe1 mediated pH(i) regulation in brain-derived glial-like cells in vitro. Furthermore, neural stem cell differentiation and neurosphere formation (proliferation) were completely inhibited by tannic acid. The present study provides evidence that tannic acid is a natural inhibitor of NBCe1. It is tempting to speculate that tannic acid or related compounds that inhibits NBCe1-mediated pHi regulation in glial-like cells may also have bearing on the treatment of glial neoplasms. |
format | Online Article Text |
id | pubmed-6903378 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-69033782020-01-22 Tannic acid inhibits electrogenic Na+/HCO3− co-transporter activity in embryonic neural stem cell-derived radial glial-like cells Nordström, Tommy Zhenyu, Gao Andersson, Leif C. Åkerman, Karl E.O. Neuroreport Cellular, Molecular and Developmental Neuroscience Self-renewing neural stem cells and progenitor cells are cell populations that generate radial glial cells and neurons through asymmetric division. Regulation of intracellular pH in stem cells with high metabolic activity is critical for both cell signaling and proliferation. We have recently found that a S0859-inhibitable electrogenic Na(+)/HCO(3)(−) co-transporter (NBCe1, Slc4a4), is the primary pH(i) regulatory mechanism in stem cell-derived radial glial-like cells. Here we show, by using the voltage-sensitive fluorescent dye DiBAC(4)(3) and BCECF, a pH-sensitive dye, that an antioxidant, tannic acid (100 µM), can inhibit potassium- and calcium-dependent rapid changes in membrane potential and NBCe1 mediated pH(i) regulation in brain-derived glial-like cells in vitro. Furthermore, neural stem cell differentiation and neurosphere formation (proliferation) were completely inhibited by tannic acid. The present study provides evidence that tannic acid is a natural inhibitor of NBCe1. It is tempting to speculate that tannic acid or related compounds that inhibits NBCe1-mediated pHi regulation in glial-like cells may also have bearing on the treatment of glial neoplasms. Lippincott Williams & Wilkins 2020-01-08 2019-11-08 /pmc/articles/PMC6903378/ /pubmed/31714480 http://dx.doi.org/10.1097/WNR.0000000000001372 Text en Copyright © 2019 The Author(s). Published by Wolters Kluwer Health, Inc. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Cellular, Molecular and Developmental Neuroscience Nordström, Tommy Zhenyu, Gao Andersson, Leif C. Åkerman, Karl E.O. Tannic acid inhibits electrogenic Na+/HCO3− co-transporter activity in embryonic neural stem cell-derived radial glial-like cells |
title | Tannic acid inhibits electrogenic Na+/HCO3− co-transporter activity in embryonic neural stem cell-derived radial glial-like cells |
title_full | Tannic acid inhibits electrogenic Na+/HCO3− co-transporter activity in embryonic neural stem cell-derived radial glial-like cells |
title_fullStr | Tannic acid inhibits electrogenic Na+/HCO3− co-transporter activity in embryonic neural stem cell-derived radial glial-like cells |
title_full_unstemmed | Tannic acid inhibits electrogenic Na+/HCO3− co-transporter activity in embryonic neural stem cell-derived radial glial-like cells |
title_short | Tannic acid inhibits electrogenic Na+/HCO3− co-transporter activity in embryonic neural stem cell-derived radial glial-like cells |
title_sort | tannic acid inhibits electrogenic na+/hco3− co-transporter activity in embryonic neural stem cell-derived radial glial-like cells |
topic | Cellular, Molecular and Developmental Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6903378/ https://www.ncbi.nlm.nih.gov/pubmed/31714480 http://dx.doi.org/10.1097/WNR.0000000000001372 |
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