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Combination of Carbonate Hydroxyapatite and Stem Cells from Human Deciduous Teeth Promotes Bone Regeneration by Enhancing BMP-2, VEGF and CD31 Expression in Immunodeficient Mice

The objective of this study was to clarify the efficiency of a combination of stem cells from human deciduous teeth and carbonate apatite in bone regeneration of calvarial defects. Immunodeficient mice (n = 5 for each group/4 groups) with artificial calvarial bone defects (5 mm in diameter) were dev...

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Autores principales: Putranti, Nurul Aisyah Rizky, Kunimatsu, Ryo, Rikitake, Kodai, Hiraki, Tomoka, Nakajima, Kengo, Abe, Takaharu, Tsuka, Yuji, Sakata, Shuzo, Nakatani, Ayaka, Nikawa, Hiroki, Tanimoto, Kotaro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9221865/
https://www.ncbi.nlm.nih.gov/pubmed/35741043
http://dx.doi.org/10.3390/cells11121914
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author Putranti, Nurul Aisyah Rizky
Kunimatsu, Ryo
Rikitake, Kodai
Hiraki, Tomoka
Nakajima, Kengo
Abe, Takaharu
Tsuka, Yuji
Sakata, Shuzo
Nakatani, Ayaka
Nikawa, Hiroki
Tanimoto, Kotaro
author_facet Putranti, Nurul Aisyah Rizky
Kunimatsu, Ryo
Rikitake, Kodai
Hiraki, Tomoka
Nakajima, Kengo
Abe, Takaharu
Tsuka, Yuji
Sakata, Shuzo
Nakatani, Ayaka
Nikawa, Hiroki
Tanimoto, Kotaro
author_sort Putranti, Nurul Aisyah Rizky
collection PubMed
description The objective of this study was to clarify the efficiency of a combination of stem cells from human deciduous teeth and carbonate apatite in bone regeneration of calvarial defects. Immunodeficient mice (n = 5 for each group/4 groups) with artificial calvarial bone defects (5 mm in diameter) were developed, and stem cells from human deciduous teeth (SHEDs) and carbonate hydroxyapatite (CAP) granules were transplanted with an atelocollagen sponge as a scaffold. A 3D analysis using microcomputed tomography, and 12 weeks after transplantation, histological and immunohistochemical evaluations of markers of bone morphogenetic protein-2 (BMP-2), vascular endothelial growth factor (VEGF), and cluster of differentiation (CD) 31 were performed. In the 3D analysis, regenerated bone formation was observed in SHEDs and CAP, with the combination of SHEDs and CAP showing significantly greater bone regeneration than that in the other groups. Histological and immunohistochemical evaluations showed that combining SHEDs and CAP enhanced the expression of BMP-2, VEGF, and CD31, and promoted bone regeneration. This study demonstrates that the combination of SHEDs and CAP transplantation may be a promising tool for bone regeneration in alveolar defects.
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spelling pubmed-92218652022-06-24 Combination of Carbonate Hydroxyapatite and Stem Cells from Human Deciduous Teeth Promotes Bone Regeneration by Enhancing BMP-2, VEGF and CD31 Expression in Immunodeficient Mice Putranti, Nurul Aisyah Rizky Kunimatsu, Ryo Rikitake, Kodai Hiraki, Tomoka Nakajima, Kengo Abe, Takaharu Tsuka, Yuji Sakata, Shuzo Nakatani, Ayaka Nikawa, Hiroki Tanimoto, Kotaro Cells Article The objective of this study was to clarify the efficiency of a combination of stem cells from human deciduous teeth and carbonate apatite in bone regeneration of calvarial defects. Immunodeficient mice (n = 5 for each group/4 groups) with artificial calvarial bone defects (5 mm in diameter) were developed, and stem cells from human deciduous teeth (SHEDs) and carbonate hydroxyapatite (CAP) granules were transplanted with an atelocollagen sponge as a scaffold. A 3D analysis using microcomputed tomography, and 12 weeks after transplantation, histological and immunohistochemical evaluations of markers of bone morphogenetic protein-2 (BMP-2), vascular endothelial growth factor (VEGF), and cluster of differentiation (CD) 31 were performed. In the 3D analysis, regenerated bone formation was observed in SHEDs and CAP, with the combination of SHEDs and CAP showing significantly greater bone regeneration than that in the other groups. Histological and immunohistochemical evaluations showed that combining SHEDs and CAP enhanced the expression of BMP-2, VEGF, and CD31, and promoted bone regeneration. This study demonstrates that the combination of SHEDs and CAP transplantation may be a promising tool for bone regeneration in alveolar defects. MDPI 2022-06-13 /pmc/articles/PMC9221865/ /pubmed/35741043 http://dx.doi.org/10.3390/cells11121914 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Putranti, Nurul Aisyah Rizky
Kunimatsu, Ryo
Rikitake, Kodai
Hiraki, Tomoka
Nakajima, Kengo
Abe, Takaharu
Tsuka, Yuji
Sakata, Shuzo
Nakatani, Ayaka
Nikawa, Hiroki
Tanimoto, Kotaro
Combination of Carbonate Hydroxyapatite and Stem Cells from Human Deciduous Teeth Promotes Bone Regeneration by Enhancing BMP-2, VEGF and CD31 Expression in Immunodeficient Mice
title Combination of Carbonate Hydroxyapatite and Stem Cells from Human Deciduous Teeth Promotes Bone Regeneration by Enhancing BMP-2, VEGF and CD31 Expression in Immunodeficient Mice
title_full Combination of Carbonate Hydroxyapatite and Stem Cells from Human Deciduous Teeth Promotes Bone Regeneration by Enhancing BMP-2, VEGF and CD31 Expression in Immunodeficient Mice
title_fullStr Combination of Carbonate Hydroxyapatite and Stem Cells from Human Deciduous Teeth Promotes Bone Regeneration by Enhancing BMP-2, VEGF and CD31 Expression in Immunodeficient Mice
title_full_unstemmed Combination of Carbonate Hydroxyapatite and Stem Cells from Human Deciduous Teeth Promotes Bone Regeneration by Enhancing BMP-2, VEGF and CD31 Expression in Immunodeficient Mice
title_short Combination of Carbonate Hydroxyapatite and Stem Cells from Human Deciduous Teeth Promotes Bone Regeneration by Enhancing BMP-2, VEGF and CD31 Expression in Immunodeficient Mice
title_sort combination of carbonate hydroxyapatite and stem cells from human deciduous teeth promotes bone regeneration by enhancing bmp-2, vegf and cd31 expression in immunodeficient mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9221865/
https://www.ncbi.nlm.nih.gov/pubmed/35741043
http://dx.doi.org/10.3390/cells11121914
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