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Heterogeneity affects the differentiation potential of dental follicle stem cells through the TGF-β signaling pathway

Adult mesenchymal stem cells play an important role in maintaining organ homeostasis owing to their unique ability to generate more specialized cell populations in a coordinated manner. Adult mesenchymal stem cells are heterogeneous, a feature that is essential for their functions. However, studies...

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Autores principales: Zhaosong, Meng, Na, Fu, Shuling, Guo, Jiacheng, Liu, Ran, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8810196/
https://www.ncbi.nlm.nih.gov/pubmed/34927533
http://dx.doi.org/10.1080/21655979.2021.2009974
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author Zhaosong, Meng
Na, Fu
Shuling, Guo
Jiacheng, Liu
Ran, Wei
author_facet Zhaosong, Meng
Na, Fu
Shuling, Guo
Jiacheng, Liu
Ran, Wei
author_sort Zhaosong, Meng
collection PubMed
description Adult mesenchymal stem cells play an important role in maintaining organ homeostasis owing to their unique ability to generate more specialized cell populations in a coordinated manner. Adult mesenchymal stem cells are heterogeneous, a feature that is essential for their functions. However, studies have not elucidated how heterogeneity of mesenchymal stem cells affects their differentiation capacity. The current study thus explored the heterogeneous Dental Follicle Stem Cells (DFSCs). A previous study by our research group reported that selecting sub-clones can cause artificial damage of the heterogeneous microenvironment of DFSCs. The finds showed a decrease in differentiation capacity of the three subclones, although the underlying mechanism was not elucidated. In this study, cells were harvested and prepared for gene expression microarray analysis. Sequence data was used in gene ontology and pathway enrichment analysis. The results showed that downregulation of the TGF-β signaling pathway was the main cause of changes in differentiation of sub-clones. Additional analyses revealed that the Hippo pathway, WNT pathway and signaling pathways regulating the pluripotency of stem cells were also implicated in these changes, through a cross talk with TGF-β signaling pathway through Bmp2, Bmp4, and Bambi. In vivo implantation experiments and osteogenic induction showed that differentiation capacity of DFSCs was significantly reduced in the sub-clones. In summary, the findings of the current study show that differentiation potential of DFSCs is correlated with the heterogeneous microenvironment and TGF-β signaling pathway significantly modulates these biological processes.
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spelling pubmed-88101962022-02-03 Heterogeneity affects the differentiation potential of dental follicle stem cells through the TGF-β signaling pathway Zhaosong, Meng Na, Fu Shuling, Guo Jiacheng, Liu Ran, Wei Bioengineered Research Paper Adult mesenchymal stem cells play an important role in maintaining organ homeostasis owing to their unique ability to generate more specialized cell populations in a coordinated manner. Adult mesenchymal stem cells are heterogeneous, a feature that is essential for their functions. However, studies have not elucidated how heterogeneity of mesenchymal stem cells affects their differentiation capacity. The current study thus explored the heterogeneous Dental Follicle Stem Cells (DFSCs). A previous study by our research group reported that selecting sub-clones can cause artificial damage of the heterogeneous microenvironment of DFSCs. The finds showed a decrease in differentiation capacity of the three subclones, although the underlying mechanism was not elucidated. In this study, cells were harvested and prepared for gene expression microarray analysis. Sequence data was used in gene ontology and pathway enrichment analysis. The results showed that downregulation of the TGF-β signaling pathway was the main cause of changes in differentiation of sub-clones. Additional analyses revealed that the Hippo pathway, WNT pathway and signaling pathways regulating the pluripotency of stem cells were also implicated in these changes, through a cross talk with TGF-β signaling pathway through Bmp2, Bmp4, and Bambi. In vivo implantation experiments and osteogenic induction showed that differentiation capacity of DFSCs was significantly reduced in the sub-clones. In summary, the findings of the current study show that differentiation potential of DFSCs is correlated with the heterogeneous microenvironment and TGF-β signaling pathway significantly modulates these biological processes. Taylor & Francis 2021-12-18 /pmc/articles/PMC8810196/ /pubmed/34927533 http://dx.doi.org/10.1080/21655979.2021.2009974 Text en © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Zhaosong, Meng
Na, Fu
Shuling, Guo
Jiacheng, Liu
Ran, Wei
Heterogeneity affects the differentiation potential of dental follicle stem cells through the TGF-β signaling pathway
title Heterogeneity affects the differentiation potential of dental follicle stem cells through the TGF-β signaling pathway
title_full Heterogeneity affects the differentiation potential of dental follicle stem cells through the TGF-β signaling pathway
title_fullStr Heterogeneity affects the differentiation potential of dental follicle stem cells through the TGF-β signaling pathway
title_full_unstemmed Heterogeneity affects the differentiation potential of dental follicle stem cells through the TGF-β signaling pathway
title_short Heterogeneity affects the differentiation potential of dental follicle stem cells through the TGF-β signaling pathway
title_sort heterogeneity affects the differentiation potential of dental follicle stem cells through the tgf-β signaling pathway
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8810196/
https://www.ncbi.nlm.nih.gov/pubmed/34927533
http://dx.doi.org/10.1080/21655979.2021.2009974
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