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Na(+) and K(+) transport and maturation stage ameloblast modulation
Introduction: Enamel mineralization requires calcium transport into the extracellular matrix for the synthesis of hydroxyapatite (HA) crystals. Formation of HA releases protons into the matrix, which are then neutralized when ameloblasts modulate from cells with apical invaginations, the so-called r...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9939811/ https://www.ncbi.nlm.nih.gov/pubmed/36814472 http://dx.doi.org/10.3389/fphys.2023.1124444 |
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author | Ngu, Jake Bronckers, Antonius L. J. J. Katsura, Kaitlin Zhang, Yan Den Besten, Pamela K. |
author_facet | Ngu, Jake Bronckers, Antonius L. J. J. Katsura, Kaitlin Zhang, Yan Den Besten, Pamela K. |
author_sort | Ngu, Jake |
collection | PubMed |
description | Introduction: Enamel mineralization requires calcium transport into the extracellular matrix for the synthesis of hydroxyapatite (HA) crystals. Formation of HA releases protons into the matrix, which are then neutralized when ameloblasts modulate from cells with apical invaginations, the so-called ruffle-ended ameloblasts (RE), to smooth-ended ameloblasts (SE). Ameloblast modulation is associated with the translocation of the calcium exchanger Nckx4 to the apical border of RE, to remove Na(+) from the enamel matrix in exchange for Ca(2+) and K(+). As enamel matures, Na(+) and K(+) in the matrix progressively decrease. However, the transporter to remove K(+) from mineralizing enamel has not been identified. Methods: Expression of K(+) exchangers and channels in secretory and maturation stage of enamel organs were compared following an RNA-seq analysis. Kcnj15, which encodes the Kir4.2 inwardly rectifying K(+) channel, was found to be the most upregulated internalizing K(+) transporter in maturation stage of enamel organs. Kir4.2 was immunolocalized in wt, Nckx4(−/−), Wdr72(−/−), and fluorosed ameloblasts. Regulation of Wdr72 expression by pH was characterized in vitro and in vivo. Results: Kir4.2 immunolocalized to the apical border of wild type (wt) mouse RE and cytosol of SE, a spatial distribution pattern shared by NCKX4. In Nckx4(−/−) ameloblasts, Kir4.2 also localized to the apical surface of RE and cytosol of SE. However, in fluorosed and Wdr72(−/−) ameloblasts, in which vesicle trafficking is disrupted, Kir4.2 remained in the cytosol. In vitro, Wdr72 was upregulated in LS8 cells cultured in medium with a pH 6.2, which is the pH of the enamel matrix underlying RE, as compared to pH 7.2 under SE. Conclusion: Taken together these results suggest that Kir4.2 participates in K(+) uptake by maturation ameloblasts, and that K(+) and Na(+) uptake by Kir4.2 and Nckx4, respectively, may be regulated by pH through WDR72-mediated endocytosis and membrane trafficking. |
format | Online Article Text |
id | pubmed-9939811 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-99398112023-02-21 Na(+) and K(+) transport and maturation stage ameloblast modulation Ngu, Jake Bronckers, Antonius L. J. J. Katsura, Kaitlin Zhang, Yan Den Besten, Pamela K. Front Physiol Physiology Introduction: Enamel mineralization requires calcium transport into the extracellular matrix for the synthesis of hydroxyapatite (HA) crystals. Formation of HA releases protons into the matrix, which are then neutralized when ameloblasts modulate from cells with apical invaginations, the so-called ruffle-ended ameloblasts (RE), to smooth-ended ameloblasts (SE). Ameloblast modulation is associated with the translocation of the calcium exchanger Nckx4 to the apical border of RE, to remove Na(+) from the enamel matrix in exchange for Ca(2+) and K(+). As enamel matures, Na(+) and K(+) in the matrix progressively decrease. However, the transporter to remove K(+) from mineralizing enamel has not been identified. Methods: Expression of K(+) exchangers and channels in secretory and maturation stage of enamel organs were compared following an RNA-seq analysis. Kcnj15, which encodes the Kir4.2 inwardly rectifying K(+) channel, was found to be the most upregulated internalizing K(+) transporter in maturation stage of enamel organs. Kir4.2 was immunolocalized in wt, Nckx4(−/−), Wdr72(−/−), and fluorosed ameloblasts. Regulation of Wdr72 expression by pH was characterized in vitro and in vivo. Results: Kir4.2 immunolocalized to the apical border of wild type (wt) mouse RE and cytosol of SE, a spatial distribution pattern shared by NCKX4. In Nckx4(−/−) ameloblasts, Kir4.2 also localized to the apical surface of RE and cytosol of SE. However, in fluorosed and Wdr72(−/−) ameloblasts, in which vesicle trafficking is disrupted, Kir4.2 remained in the cytosol. In vitro, Wdr72 was upregulated in LS8 cells cultured in medium with a pH 6.2, which is the pH of the enamel matrix underlying RE, as compared to pH 7.2 under SE. Conclusion: Taken together these results suggest that Kir4.2 participates in K(+) uptake by maturation ameloblasts, and that K(+) and Na(+) uptake by Kir4.2 and Nckx4, respectively, may be regulated by pH through WDR72-mediated endocytosis and membrane trafficking. Frontiers Media S.A. 2023-02-06 /pmc/articles/PMC9939811/ /pubmed/36814472 http://dx.doi.org/10.3389/fphys.2023.1124444 Text en Copyright © 2023 Ngu, Bronckers, Katsura, Zhang and Den Besten. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Physiology Ngu, Jake Bronckers, Antonius L. J. J. Katsura, Kaitlin Zhang, Yan Den Besten, Pamela K. Na(+) and K(+) transport and maturation stage ameloblast modulation |
title | Na(+) and K(+) transport and maturation stage ameloblast modulation |
title_full | Na(+) and K(+) transport and maturation stage ameloblast modulation |
title_fullStr | Na(+) and K(+) transport and maturation stage ameloblast modulation |
title_full_unstemmed | Na(+) and K(+) transport and maturation stage ameloblast modulation |
title_short | Na(+) and K(+) transport and maturation stage ameloblast modulation |
title_sort | na(+) and k(+) transport and maturation stage ameloblast modulation |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9939811/ https://www.ncbi.nlm.nih.gov/pubmed/36814472 http://dx.doi.org/10.3389/fphys.2023.1124444 |
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