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Biological Behavioral Alterations of the Post-neural Differentiated Dental Pulp Stem Cells Through an in situ Microenvironment

Transplantation of undifferentiated dental pulp stem cells (DPSCs) may suffer from tumorigenesis. Neuronal differentiated DPSCs (d-DPSCs) have emerged as an ideal source to treat central nervous system (CNS) disorders. Moreover, different components of culture medium functioned on the characteristic...

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Autores principales: Luo, Lihua, Wang, Xiaoyan, Zhang, Yanni, Wu, Yuwei, Hu, Fengting, Xing, Zhenjie, Wang, Lei, Xiao, Jian, Guastaldi, Fernando, He, Yan, Ye, Qingsong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7744789/
https://www.ncbi.nlm.nih.gov/pubmed/33344464
http://dx.doi.org/10.3389/fcell.2020.625151
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author Luo, Lihua
Wang, Xiaoyan
Zhang, Yanni
Wu, Yuwei
Hu, Fengting
Xing, Zhenjie
Wang, Lei
Xiao, Jian
Guastaldi, Fernando
He, Yan
Ye, Qingsong
author_facet Luo, Lihua
Wang, Xiaoyan
Zhang, Yanni
Wu, Yuwei
Hu, Fengting
Xing, Zhenjie
Wang, Lei
Xiao, Jian
Guastaldi, Fernando
He, Yan
Ye, Qingsong
author_sort Luo, Lihua
collection PubMed
description Transplantation of undifferentiated dental pulp stem cells (DPSCs) may suffer from tumorigenesis. Neuronal differentiated DPSCs (d-DPSCs) have emerged as an ideal source to treat central nervous system (CNS) disorders. Moreover, different components of culture medium functioned on the characteristics of d-DPSCs in vitro. In this study, d-DPSCs were cultured in three types of medium: Neurobasal(®®)-A medium supplemented with 2% B27 (the 2% B27 NM group), Neurobasal(®) -A medium supplemented with 2% B27 and 5% FBS (the 2% B27 + 5% FBS NM group), and α-MEM containing 10% FBS (the 10% FBS α-MEM group). We found that d-DPSCs in the 2% B27 + 5% FBS NM group had lower proliferation and reduced expression of transient receptor potential canonical 1 (TRPC1) and CD146, whereas up-regulated Nestin and microtubule-associated protein-2 (MAP-2). Notably, d-DPSCs in the 10% FBS α-MEM group possessed high proliferative capacity, decreased expression of neuron-like markers and partially restored stemness. It was demonstrated that d-DPSCs cultured in the 2% B27 + 5% FBS NM could maintain their neuron-like characteristics. Besides, d-DPSCs cultivated in the 10% FBS α-MEM could partially recover their stem cells properties, indicating that neural differentiation of DPSCs was reversible and could open novel avenues for exploring the pluripotency of DPSCs.
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spelling pubmed-77447892020-12-18 Biological Behavioral Alterations of the Post-neural Differentiated Dental Pulp Stem Cells Through an in situ Microenvironment Luo, Lihua Wang, Xiaoyan Zhang, Yanni Wu, Yuwei Hu, Fengting Xing, Zhenjie Wang, Lei Xiao, Jian Guastaldi, Fernando He, Yan Ye, Qingsong Front Cell Dev Biol Cell and Developmental Biology Transplantation of undifferentiated dental pulp stem cells (DPSCs) may suffer from tumorigenesis. Neuronal differentiated DPSCs (d-DPSCs) have emerged as an ideal source to treat central nervous system (CNS) disorders. Moreover, different components of culture medium functioned on the characteristics of d-DPSCs in vitro. In this study, d-DPSCs were cultured in three types of medium: Neurobasal(®®)-A medium supplemented with 2% B27 (the 2% B27 NM group), Neurobasal(®) -A medium supplemented with 2% B27 and 5% FBS (the 2% B27 + 5% FBS NM group), and α-MEM containing 10% FBS (the 10% FBS α-MEM group). We found that d-DPSCs in the 2% B27 + 5% FBS NM group had lower proliferation and reduced expression of transient receptor potential canonical 1 (TRPC1) and CD146, whereas up-regulated Nestin and microtubule-associated protein-2 (MAP-2). Notably, d-DPSCs in the 10% FBS α-MEM group possessed high proliferative capacity, decreased expression of neuron-like markers and partially restored stemness. It was demonstrated that d-DPSCs cultured in the 2% B27 + 5% FBS NM could maintain their neuron-like characteristics. Besides, d-DPSCs cultivated in the 10% FBS α-MEM could partially recover their stem cells properties, indicating that neural differentiation of DPSCs was reversible and could open novel avenues for exploring the pluripotency of DPSCs. Frontiers Media S.A. 2020-12-03 /pmc/articles/PMC7744789/ /pubmed/33344464 http://dx.doi.org/10.3389/fcell.2020.625151 Text en Copyright © 2020 Luo, Wang, Zhang, Wu, Hu, Xing, Wang, Xiao, Guastaldi, He and Ye. http://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 Cell and Developmental Biology
Luo, Lihua
Wang, Xiaoyan
Zhang, Yanni
Wu, Yuwei
Hu, Fengting
Xing, Zhenjie
Wang, Lei
Xiao, Jian
Guastaldi, Fernando
He, Yan
Ye, Qingsong
Biological Behavioral Alterations of the Post-neural Differentiated Dental Pulp Stem Cells Through an in situ Microenvironment
title Biological Behavioral Alterations of the Post-neural Differentiated Dental Pulp Stem Cells Through an in situ Microenvironment
title_full Biological Behavioral Alterations of the Post-neural Differentiated Dental Pulp Stem Cells Through an in situ Microenvironment
title_fullStr Biological Behavioral Alterations of the Post-neural Differentiated Dental Pulp Stem Cells Through an in situ Microenvironment
title_full_unstemmed Biological Behavioral Alterations of the Post-neural Differentiated Dental Pulp Stem Cells Through an in situ Microenvironment
title_short Biological Behavioral Alterations of the Post-neural Differentiated Dental Pulp Stem Cells Through an in situ Microenvironment
title_sort biological behavioral alterations of the post-neural differentiated dental pulp stem cells through an in situ microenvironment
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7744789/
https://www.ncbi.nlm.nih.gov/pubmed/33344464
http://dx.doi.org/10.3389/fcell.2020.625151
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