Characterization of Living Dental Pulp Cells in Direct Contact with Mineral Trioxide Aggregate

Mineral trioxide aggregate (MTA) was introduced as a material for dental endodontic regenerative therapy. Here, we show the dynamics of living dental pulp cells in direct contact with an MTA disk. A red fluorescence protein (DsRed) was introduced into immortalized porcine dental pulp cells (PPU7) an...

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Main Authors: Tamaki Hattori-Sanuki, Takeo Karakida, Risako Chiba-Ohkuma, Yasuo Miake, Ryuji Yamamoto, Yasuo Yamakoshi, Noriyasu Hosoya
Format: Article
Language:English
Published: MDPI AG 2020-10-01
Series:Cells
Subjects:
Online Access:https://www.mdpi.com/2073-4409/9/10/2336
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author Tamaki Hattori-Sanuki
Takeo Karakida
Risako Chiba-Ohkuma
Yasuo Miake
Ryuji Yamamoto
Yasuo Yamakoshi
Noriyasu Hosoya
author_facet Tamaki Hattori-Sanuki
Takeo Karakida
Risako Chiba-Ohkuma
Yasuo Miake
Ryuji Yamamoto
Yasuo Yamakoshi
Noriyasu Hosoya
author_sort Tamaki Hattori-Sanuki
collection DOAJ
description Mineral trioxide aggregate (MTA) was introduced as a material for dental endodontic regenerative therapy. Here, we show the dynamics of living dental pulp cells in direct contact with an MTA disk. A red fluorescence protein (DsRed) was introduced into immortalized porcine dental pulp cells (PPU7) and cloned. DsRed-PPU7 cells were cultured on the MTA disk and cell proliferation, chemotaxis, the effects of growth factors and the gene expression of cells were investigated at the biological, histomorphological and genetic cell levels. Mineralized precipitates formed in the DsRed-PPU7 cells were characterized with crystal structural analysis. DsRed-PPU7 cells proliferated in the central part of the MTA disk until Day 6 and displayed a tendency to move to the outer circumference. Both transforming growth factor beta and bone morphogenetic protein promoted the proliferation and movement of DsRed-PPU7 cells and also enhanced the expression levels of odontoblastic gene differentiation markers. Mineralized precipitates formed in DsRed-PPU7 were composed of calcium and phosphate but its crystals were different in each position. Our investigation showed that DsRed-PPU7 cells in direct contact with the MTA disk could differentiate into odontoblasts by controlling cell–cell and cell–substrate interactions depending on cell adhesion and the surrounding environment of the MTA.
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spelling doaj.art-1870448dd86441c28ac89df685bfc1ca2023-11-20T17:59:28ZengMDPI AGCells2073-44092020-10-01910233610.3390/cells9102336Characterization of Living Dental Pulp Cells in Direct Contact with Mineral Trioxide AggregateTamaki Hattori-Sanuki0Takeo Karakida1Risako Chiba-Ohkuma2Yasuo Miake3Ryuji Yamamoto4Yasuo Yamakoshi5Noriyasu Hosoya6Department of Endodontology, School of Dental Medicine, Tsurumi University, 2-1-3 Tsurumi, Tsurumi-ku, Yokohama 230-8501, JapanDepartment of Biochemistry and Molecular Biology, School of Dental Medicine, Tsurumi University, 2-1-3 Tsurumi, Tsurumi-ku, Yokohama 230-8501, JapanDepartment of Biochemistry and Molecular Biology, School of Dental Medicine, Tsurumi University, 2-1-3 Tsurumi, Tsurumi-ku, Yokohama 230-8501, JapanDepartment of Anatomy, School of Dental Medicine, Tsurumi University, 2-1-3 Tsurumi, Tsurumi-ku, Yokohama 230-8501, JapanDepartment of Biochemistry and Molecular Biology, School of Dental Medicine, Tsurumi University, 2-1-3 Tsurumi, Tsurumi-ku, Yokohama 230-8501, JapanDepartment of Biochemistry and Molecular Biology, School of Dental Medicine, Tsurumi University, 2-1-3 Tsurumi, Tsurumi-ku, Yokohama 230-8501, JapanDepartment of Endodontology, School of Dental Medicine, Tsurumi University, 2-1-3 Tsurumi, Tsurumi-ku, Yokohama 230-8501, JapanMineral trioxide aggregate (MTA) was introduced as a material for dental endodontic regenerative therapy. Here, we show the dynamics of living dental pulp cells in direct contact with an MTA disk. A red fluorescence protein (DsRed) was introduced into immortalized porcine dental pulp cells (PPU7) and cloned. DsRed-PPU7 cells were cultured on the MTA disk and cell proliferation, chemotaxis, the effects of growth factors and the gene expression of cells were investigated at the biological, histomorphological and genetic cell levels. Mineralized precipitates formed in the DsRed-PPU7 cells were characterized with crystal structural analysis. DsRed-PPU7 cells proliferated in the central part of the MTA disk until Day 6 and displayed a tendency to move to the outer circumference. Both transforming growth factor beta and bone morphogenetic protein promoted the proliferation and movement of DsRed-PPU7 cells and also enhanced the expression levels of odontoblastic gene differentiation markers. Mineralized precipitates formed in DsRed-PPU7 were composed of calcium and phosphate but its crystals were different in each position. Our investigation showed that DsRed-PPU7 cells in direct contact with the MTA disk could differentiate into odontoblasts by controlling cell–cell and cell–substrate interactions depending on cell adhesion and the surrounding environment of the MTA.https://www.mdpi.com/2073-4409/9/10/2336mineral trioxide aggregatedental pulp cellsfluorescent labelingcell chemotaxiscalcium phosphate crystal
spellingShingle Tamaki Hattori-Sanuki
Takeo Karakida
Risako Chiba-Ohkuma
Yasuo Miake
Ryuji Yamamoto
Yasuo Yamakoshi
Noriyasu Hosoya
Characterization of Living Dental Pulp Cells in Direct Contact with Mineral Trioxide Aggregate
Cells
mineral trioxide aggregate
dental pulp cells
fluorescent labeling
cell chemotaxis
calcium phosphate crystal
title Characterization of Living Dental Pulp Cells in Direct Contact with Mineral Trioxide Aggregate
title_full Characterization of Living Dental Pulp Cells in Direct Contact with Mineral Trioxide Aggregate
title_fullStr Characterization of Living Dental Pulp Cells in Direct Contact with Mineral Trioxide Aggregate
title_full_unstemmed Characterization of Living Dental Pulp Cells in Direct Contact with Mineral Trioxide Aggregate
title_short Characterization of Living Dental Pulp Cells in Direct Contact with Mineral Trioxide Aggregate
title_sort characterization of living dental pulp cells in direct contact with mineral trioxide aggregate
topic mineral trioxide aggregate
dental pulp cells
fluorescent labeling
cell chemotaxis
calcium phosphate crystal
url https://www.mdpi.com/2073-4409/9/10/2336
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AT yasuomiake characterizationoflivingdentalpulpcellsindirectcontactwithmineraltrioxideaggregate
AT ryujiyamamoto characterizationoflivingdentalpulpcellsindirectcontactwithmineraltrioxideaggregate
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