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Comparison of Odontogenic Differentiation of Human Dental Follicle Cells and Human Dental Papilla Cells
Classical tooth development theory suggests that dental papilla cells (DPCs) are the precursor cells of odontoblasts, which are responsible for dentin development. However, our previous studies have indicated that dental follicle cells (DFCs) can differentiate into odontoblasts. To further our under...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3631153/ https://www.ncbi.nlm.nih.gov/pubmed/23620822 http://dx.doi.org/10.1371/journal.pone.0062332 |
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author | Guo, Lijuan Li, Jie Qiao, Xiangchen Yu, Mei Tang, Wei Wang, Hang Guo, Weihua Tian, Weidong |
author_facet | Guo, Lijuan Li, Jie Qiao, Xiangchen Yu, Mei Tang, Wei Wang, Hang Guo, Weihua Tian, Weidong |
author_sort | Guo, Lijuan |
collection | PubMed |
description | Classical tooth development theory suggests that dental papilla cells (DPCs) are the precursor cells of odontoblasts, which are responsible for dentin development. However, our previous studies have indicated that dental follicle cells (DFCs) can differentiate into odontoblasts. To further our understanding of tooth development, and the differences in dentinogenesis between DFCs and DPCs, the odontogenic differentiation of DFCs and DPCs was characterized in vitro and in vivo. DFCs and DPCs were individually combined with treated dentin matrix (TDM) before they were subcutaneously implanted into the dorsum of mice for 8 weeks. Results showed that 12 proteins were significantly differential, and phosphoserine aminotransferase 1 (PSAT1), Isoform 2 of hypoxia-inducible factor 1-alpha (HIF1A) and Isoform 1 of annexin A2 (ANXA2), were the most significantly differential proteins. These proteins are related to regulation of bone balance, angiogenesis and cell survival in an anoxic environment. Both DFCs and DPCs express odontogenic, neurogenic and peridontogenic markers. Histological examination of the harvested grafts showed that both DFCs and DPCs form pulp-dentin/cementum-periodentium-like tissues in vivo. Hence, DFCs and DPCs have similar odontogenic differentiation potential in the presence of TDM. However, differences in glucose and amino acid metabolism signal transduction and protein synthesis were observed for the two cell types. This study expands our understanding on tooth development, and provides direct evidence for the use of alternative cell sources in tooth regeneration. |
format | Online Article Text |
id | pubmed-3631153 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-36311532013-04-25 Comparison of Odontogenic Differentiation of Human Dental Follicle Cells and Human Dental Papilla Cells Guo, Lijuan Li, Jie Qiao, Xiangchen Yu, Mei Tang, Wei Wang, Hang Guo, Weihua Tian, Weidong PLoS One Research Article Classical tooth development theory suggests that dental papilla cells (DPCs) are the precursor cells of odontoblasts, which are responsible for dentin development. However, our previous studies have indicated that dental follicle cells (DFCs) can differentiate into odontoblasts. To further our understanding of tooth development, and the differences in dentinogenesis between DFCs and DPCs, the odontogenic differentiation of DFCs and DPCs was characterized in vitro and in vivo. DFCs and DPCs were individually combined with treated dentin matrix (TDM) before they were subcutaneously implanted into the dorsum of mice for 8 weeks. Results showed that 12 proteins were significantly differential, and phosphoserine aminotransferase 1 (PSAT1), Isoform 2 of hypoxia-inducible factor 1-alpha (HIF1A) and Isoform 1 of annexin A2 (ANXA2), were the most significantly differential proteins. These proteins are related to regulation of bone balance, angiogenesis and cell survival in an anoxic environment. Both DFCs and DPCs express odontogenic, neurogenic and peridontogenic markers. Histological examination of the harvested grafts showed that both DFCs and DPCs form pulp-dentin/cementum-periodentium-like tissues in vivo. Hence, DFCs and DPCs have similar odontogenic differentiation potential in the presence of TDM. However, differences in glucose and amino acid metabolism signal transduction and protein synthesis were observed for the two cell types. This study expands our understanding on tooth development, and provides direct evidence for the use of alternative cell sources in tooth regeneration. Public Library of Science 2013-04-19 /pmc/articles/PMC3631153/ /pubmed/23620822 http://dx.doi.org/10.1371/journal.pone.0062332 Text en © 2013 Guo, et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Guo, Lijuan Li, Jie Qiao, Xiangchen Yu, Mei Tang, Wei Wang, Hang Guo, Weihua Tian, Weidong Comparison of Odontogenic Differentiation of Human Dental Follicle Cells and Human Dental Papilla Cells |
title | Comparison of Odontogenic Differentiation of Human Dental Follicle Cells and Human Dental Papilla Cells |
title_full | Comparison of Odontogenic Differentiation of Human Dental Follicle Cells and Human Dental Papilla Cells |
title_fullStr | Comparison of Odontogenic Differentiation of Human Dental Follicle Cells and Human Dental Papilla Cells |
title_full_unstemmed | Comparison of Odontogenic Differentiation of Human Dental Follicle Cells and Human Dental Papilla Cells |
title_short | Comparison of Odontogenic Differentiation of Human Dental Follicle Cells and Human Dental Papilla Cells |
title_sort | comparison of odontogenic differentiation of human dental follicle cells and human dental papilla cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3631153/ https://www.ncbi.nlm.nih.gov/pubmed/23620822 http://dx.doi.org/10.1371/journal.pone.0062332 |
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