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BMP7 and EREG Contribute to the Inductive Potential of Dental Mesenchyme
Odontogenesis is accomplished by reciprocal signaling between the epithelial and mesenchymal compartments. It is generally accepted that the inductive mesenchyme is capable of inducing the odontogenic commitment of both dental and non-dental epithelial cells. However, the duration of this signal in...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4424660/ https://www.ncbi.nlm.nih.gov/pubmed/25952286 http://dx.doi.org/10.1038/srep09903 |
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author | Gao, Bo Zhou, Xin Zhou, Xuedong Pi, Caixia Xu, Ruoshi Wan, Mian Yang, Jing Zhou, Yue Liu, Chengcheng Sun, Jianxun Zhang, Yan Zheng, Liwei |
author_facet | Gao, Bo Zhou, Xin Zhou, Xuedong Pi, Caixia Xu, Ruoshi Wan, Mian Yang, Jing Zhou, Yue Liu, Chengcheng Sun, Jianxun Zhang, Yan Zheng, Liwei |
author_sort | Gao, Bo |
collection | PubMed |
description | Odontogenesis is accomplished by reciprocal signaling between the epithelial and mesenchymal compartments. It is generally accepted that the inductive mesenchyme is capable of inducing the odontogenic commitment of both dental and non-dental epithelial cells. However, the duration of this signal in the developing dental mesenchyme and whether adult dental pulp tissue maintains its inductive capability remain unclear. This study investigated the contribution of growth factors to regulating the inductive potential of the dental mesenchyme. Human oral epithelial cells (OEs) were co-cultured with either human dental mesenchymal/papilla cells (FDPCs) or human dental pulp cells (ADPCs) under 2-dimensional or 3-dimensional conditions. Odontogenic-associated genes and proteins were detected by qPCR and immunofluorescence, respectively, and significant differences were observed between the two co-culture systems. The BMP7 and EREG expression levels in FDPCs were significantly higher than in ADPCs, as indicated by human growth factor PCR arrays and immunofluorescence analyses. OEs co-cultured with ADPCs supplemented with BMP7 and EREG expressed ameloblastic differentiation genes. Our study suggests that BMP7 and EREG expression in late bell-stage human dental papilla contributes to the inductive potential of dental mesenchyme. Furthermore, adult dental pulp cells supplemented with these two growth factors re-established the inductive potential of postnatal dental pulp tissue. |
format | Online Article Text |
id | pubmed-4424660 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-44246602015-05-13 BMP7 and EREG Contribute to the Inductive Potential of Dental Mesenchyme Gao, Bo Zhou, Xin Zhou, Xuedong Pi, Caixia Xu, Ruoshi Wan, Mian Yang, Jing Zhou, Yue Liu, Chengcheng Sun, Jianxun Zhang, Yan Zheng, Liwei Sci Rep Article Odontogenesis is accomplished by reciprocal signaling between the epithelial and mesenchymal compartments. It is generally accepted that the inductive mesenchyme is capable of inducing the odontogenic commitment of both dental and non-dental epithelial cells. However, the duration of this signal in the developing dental mesenchyme and whether adult dental pulp tissue maintains its inductive capability remain unclear. This study investigated the contribution of growth factors to regulating the inductive potential of the dental mesenchyme. Human oral epithelial cells (OEs) were co-cultured with either human dental mesenchymal/papilla cells (FDPCs) or human dental pulp cells (ADPCs) under 2-dimensional or 3-dimensional conditions. Odontogenic-associated genes and proteins were detected by qPCR and immunofluorescence, respectively, and significant differences were observed between the two co-culture systems. The BMP7 and EREG expression levels in FDPCs were significantly higher than in ADPCs, as indicated by human growth factor PCR arrays and immunofluorescence analyses. OEs co-cultured with ADPCs supplemented with BMP7 and EREG expressed ameloblastic differentiation genes. Our study suggests that BMP7 and EREG expression in late bell-stage human dental papilla contributes to the inductive potential of dental mesenchyme. Furthermore, adult dental pulp cells supplemented with these two growth factors re-established the inductive potential of postnatal dental pulp tissue. Nature Publishing Group 2015-05-08 /pmc/articles/PMC4424660/ /pubmed/25952286 http://dx.doi.org/10.1038/srep09903 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Gao, Bo Zhou, Xin Zhou, Xuedong Pi, Caixia Xu, Ruoshi Wan, Mian Yang, Jing Zhou, Yue Liu, Chengcheng Sun, Jianxun Zhang, Yan Zheng, Liwei BMP7 and EREG Contribute to the Inductive Potential of Dental Mesenchyme |
title | BMP7 and EREG Contribute to the Inductive Potential of Dental Mesenchyme |
title_full | BMP7 and EREG Contribute to the Inductive Potential of Dental Mesenchyme |
title_fullStr | BMP7 and EREG Contribute to the Inductive Potential of Dental Mesenchyme |
title_full_unstemmed | BMP7 and EREG Contribute to the Inductive Potential of Dental Mesenchyme |
title_short | BMP7 and EREG Contribute to the Inductive Potential of Dental Mesenchyme |
title_sort | bmp7 and ereg contribute to the inductive potential of dental mesenchyme |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4424660/ https://www.ncbi.nlm.nih.gov/pubmed/25952286 http://dx.doi.org/10.1038/srep09903 |
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