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Investigating the Effects of Conditioned Media from Stem Cells of Human Exfoliated Deciduous Teeth on Dental Pulp Stem Cells

Pulp regeneration has recently attracted interest in modern dentistry. However, the success ratio of pulp regeneration is low due to the compromising potential of stem cells, such as their survival, migration, and odontoblastic differentiation. Stem cells from human exfoliated deciduous teeth (SHED)...

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Autores principales: Vu, Huong Thu, Han, Mi-Ran, Lee, Jun-Haeng, Kim, Jong-Soo, Shin, Ji-Sun, Yoon, Ji-Young, Park, Jeong-Hui, Dashnyam, Khandmaa, Knowles, Jonathan Campbell, Lee, Hae-Hyoung, Kim, Jong-Bin, Lee, Jung-Hwan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9027398/
https://www.ncbi.nlm.nih.gov/pubmed/35453661
http://dx.doi.org/10.3390/biomedicines10040906
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author Vu, Huong Thu
Han, Mi-Ran
Lee, Jun-Haeng
Kim, Jong-Soo
Shin, Ji-Sun
Yoon, Ji-Young
Park, Jeong-Hui
Dashnyam, Khandmaa
Knowles, Jonathan Campbell
Lee, Hae-Hyoung
Kim, Jong-Bin
Lee, Jung-Hwan
author_facet Vu, Huong Thu
Han, Mi-Ran
Lee, Jun-Haeng
Kim, Jong-Soo
Shin, Ji-Sun
Yoon, Ji-Young
Park, Jeong-Hui
Dashnyam, Khandmaa
Knowles, Jonathan Campbell
Lee, Hae-Hyoung
Kim, Jong-Bin
Lee, Jung-Hwan
author_sort Vu, Huong Thu
collection PubMed
description Pulp regeneration has recently attracted interest in modern dentistry. However, the success ratio of pulp regeneration is low due to the compromising potential of stem cells, such as their survival, migration, and odontoblastic differentiation. Stem cells from human exfoliated deciduous teeth (SHED) have been considered a promising tool for regenerative therapy due to their ability to secrete multiple factors that are essential for tissue regeneration, which is achieved by minimally invasive procedures with fewer ethical or legal concerns than those of other procedures. The aim of this study is to investigate the potency of SHED-derived conditioned media (SHED CM) on dental pulp stem cells (DPSCs), a major type of mesenchymal stem cells for dental pulp regeneration. Our results show the promotive efficiency of SHED CM on the proliferation, survival rate, and migration of DPSCs in a dose-dependent manner. Upregulation of odontoblast/osteogenic-related marker genes, such as ALP, DSPP, DMP1, OCN, and RUNX2, and enhanced mineral deposition of impaired DPSCs are also observed in the presence of SHED CM. The analysis of SHED CM found that a variety of cytokines and growth factors have positive effects on cell proliferation, migration, anti-apoptosis, and odontoblast/osteogenic differentiation. These findings suggest that SHED CM could provide some benefits to DPSCs in pulp regeneration.
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spelling pubmed-90273982022-04-23 Investigating the Effects of Conditioned Media from Stem Cells of Human Exfoliated Deciduous Teeth on Dental Pulp Stem Cells Vu, Huong Thu Han, Mi-Ran Lee, Jun-Haeng Kim, Jong-Soo Shin, Ji-Sun Yoon, Ji-Young Park, Jeong-Hui Dashnyam, Khandmaa Knowles, Jonathan Campbell Lee, Hae-Hyoung Kim, Jong-Bin Lee, Jung-Hwan Biomedicines Article Pulp regeneration has recently attracted interest in modern dentistry. However, the success ratio of pulp regeneration is low due to the compromising potential of stem cells, such as their survival, migration, and odontoblastic differentiation. Stem cells from human exfoliated deciduous teeth (SHED) have been considered a promising tool for regenerative therapy due to their ability to secrete multiple factors that are essential for tissue regeneration, which is achieved by minimally invasive procedures with fewer ethical or legal concerns than those of other procedures. The aim of this study is to investigate the potency of SHED-derived conditioned media (SHED CM) on dental pulp stem cells (DPSCs), a major type of mesenchymal stem cells for dental pulp regeneration. Our results show the promotive efficiency of SHED CM on the proliferation, survival rate, and migration of DPSCs in a dose-dependent manner. Upregulation of odontoblast/osteogenic-related marker genes, such as ALP, DSPP, DMP1, OCN, and RUNX2, and enhanced mineral deposition of impaired DPSCs are also observed in the presence of SHED CM. The analysis of SHED CM found that a variety of cytokines and growth factors have positive effects on cell proliferation, migration, anti-apoptosis, and odontoblast/osteogenic differentiation. These findings suggest that SHED CM could provide some benefits to DPSCs in pulp regeneration. MDPI 2022-04-15 /pmc/articles/PMC9027398/ /pubmed/35453661 http://dx.doi.org/10.3390/biomedicines10040906 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
Vu, Huong Thu
Han, Mi-Ran
Lee, Jun-Haeng
Kim, Jong-Soo
Shin, Ji-Sun
Yoon, Ji-Young
Park, Jeong-Hui
Dashnyam, Khandmaa
Knowles, Jonathan Campbell
Lee, Hae-Hyoung
Kim, Jong-Bin
Lee, Jung-Hwan
Investigating the Effects of Conditioned Media from Stem Cells of Human Exfoliated Deciduous Teeth on Dental Pulp Stem Cells
title Investigating the Effects of Conditioned Media from Stem Cells of Human Exfoliated Deciduous Teeth on Dental Pulp Stem Cells
title_full Investigating the Effects of Conditioned Media from Stem Cells of Human Exfoliated Deciduous Teeth on Dental Pulp Stem Cells
title_fullStr Investigating the Effects of Conditioned Media from Stem Cells of Human Exfoliated Deciduous Teeth on Dental Pulp Stem Cells
title_full_unstemmed Investigating the Effects of Conditioned Media from Stem Cells of Human Exfoliated Deciduous Teeth on Dental Pulp Stem Cells
title_short Investigating the Effects of Conditioned Media from Stem Cells of Human Exfoliated Deciduous Teeth on Dental Pulp Stem Cells
title_sort investigating the effects of conditioned media from stem cells of human exfoliated deciduous teeth on dental pulp stem cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9027398/
https://www.ncbi.nlm.nih.gov/pubmed/35453661
http://dx.doi.org/10.3390/biomedicines10040906
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