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Dentinogenesis and Tooth-Alveolar Bone Complex Defects in BMP9/GDF2 Knockout Mice

Tooth development is regulated by sequential and reciprocal epithelium-mesenchymal interactions and their related molecular signaling pathways, such as bone morphogenetic proteins (BMPs). Among the 14 types of BMPs, BMP9 (also known as growth differentiation factor 2) is one of the most potent BMPs...

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Autores principales: Huang, Xia, Wang, Feilong, Zhao, Chen, Yang, Sheng, Cheng, Qianyu, Tang, Yingying, Zhang, Fugui, Zhang, Yan, Luo, Wenping, Wang, Chao, Zhou, Pengfei, Kim, Stephanie, Zuo, Guowei, Hu, Ning, Li, Ruidong, He, Tong-chuan, Zhang, Hongmei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mary Ann Liebert, Inc., publishers 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6534167/
https://www.ncbi.nlm.nih.gov/pubmed/30816068
http://dx.doi.org/10.1089/scd.2018.0230
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author Huang, Xia
Wang, Feilong
Zhao, Chen
Yang, Sheng
Cheng, Qianyu
Tang, Yingying
Zhang, Fugui
Zhang, Yan
Luo, Wenping
Wang, Chao
Zhou, Pengfei
Kim, Stephanie
Zuo, Guowei
Hu, Ning
Li, Ruidong
He, Tong-chuan
Zhang, Hongmei
author_facet Huang, Xia
Wang, Feilong
Zhao, Chen
Yang, Sheng
Cheng, Qianyu
Tang, Yingying
Zhang, Fugui
Zhang, Yan
Luo, Wenping
Wang, Chao
Zhou, Pengfei
Kim, Stephanie
Zuo, Guowei
Hu, Ning
Li, Ruidong
He, Tong-chuan
Zhang, Hongmei
author_sort Huang, Xia
collection PubMed
description Tooth development is regulated by sequential and reciprocal epithelium-mesenchymal interactions and their related molecular signaling pathways, such as bone morphogenetic proteins (BMPs). Among the 14 types of BMPs, BMP9 (also known as growth differentiation factor 2) is one of the most potent BMPs to induce osteogenic differentiation of mesenchymal stem cells. The purpose of this study was to examine potential roles of BMP9 signaling in tooth development. First, we detected the expression pattern of BMP9 in tooth germ during postnatal tooth development, and we found that BMP9 was widely expressed in odontoblasts, ameloblasts, dental pulp cells, and osteoblasts in alveolar bones. Then, we established a BMP9-KO mouse model. Gross morphological examination revealed that the tooth cusps of BMP9-KO mice were significantly abraded with shorter roots. Micro-computed tomography and three-dimensional reconstruction analysis indicated that the first molars of the BMP9-KO mice exhibited a reduced thickness dentin, enlarged pulp canals, and shortened roots, resembling the phenotypes of the common hereditary dental disease dentinogenesis imperfecta. Further, the alveolar bone of the BMP9-KO mutants was found to be shorter and had a decreased mineral density and trabecular thickness and bone volume fraction compared with that of the wild-type control. Mechanistically, we demonstrated that both dentin sialophosphoprotein and dentin matrix protein 1 were induced in dental stem cells by BMP9, whereas their expression was reduced when BMP9 was silenced. Further studies are required to determine whether loss of or decreased BMP9 expression is clinically associated with dentinogenesis imperfecta. Collectively, our results strongly suggest that BMP9 may play an important role in regulating dentinogenesis and tooth development. Further research is recommended into the therapeutic uses of BMP9 to regenerate traumatized and diseased tissues and for the bioengineering of replacement teeth.
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spelling pubmed-65341672019-05-28 Dentinogenesis and Tooth-Alveolar Bone Complex Defects in BMP9/GDF2 Knockout Mice Huang, Xia Wang, Feilong Zhao, Chen Yang, Sheng Cheng, Qianyu Tang, Yingying Zhang, Fugui Zhang, Yan Luo, Wenping Wang, Chao Zhou, Pengfei Kim, Stephanie Zuo, Guowei Hu, Ning Li, Ruidong He, Tong-chuan Zhang, Hongmei Stem Cells Dev Original Research Reports Tooth development is regulated by sequential and reciprocal epithelium-mesenchymal interactions and their related molecular signaling pathways, such as bone morphogenetic proteins (BMPs). Among the 14 types of BMPs, BMP9 (also known as growth differentiation factor 2) is one of the most potent BMPs to induce osteogenic differentiation of mesenchymal stem cells. The purpose of this study was to examine potential roles of BMP9 signaling in tooth development. First, we detected the expression pattern of BMP9 in tooth germ during postnatal tooth development, and we found that BMP9 was widely expressed in odontoblasts, ameloblasts, dental pulp cells, and osteoblasts in alveolar bones. Then, we established a BMP9-KO mouse model. Gross morphological examination revealed that the tooth cusps of BMP9-KO mice were significantly abraded with shorter roots. Micro-computed tomography and three-dimensional reconstruction analysis indicated that the first molars of the BMP9-KO mice exhibited a reduced thickness dentin, enlarged pulp canals, and shortened roots, resembling the phenotypes of the common hereditary dental disease dentinogenesis imperfecta. Further, the alveolar bone of the BMP9-KO mutants was found to be shorter and had a decreased mineral density and trabecular thickness and bone volume fraction compared with that of the wild-type control. Mechanistically, we demonstrated that both dentin sialophosphoprotein and dentin matrix protein 1 were induced in dental stem cells by BMP9, whereas their expression was reduced when BMP9 was silenced. Further studies are required to determine whether loss of or decreased BMP9 expression is clinically associated with dentinogenesis imperfecta. Collectively, our results strongly suggest that BMP9 may play an important role in regulating dentinogenesis and tooth development. Further research is recommended into the therapeutic uses of BMP9 to regenerate traumatized and diseased tissues and for the bioengineering of replacement teeth. Mary Ann Liebert, Inc., publishers 2019-05-15 2019-05-13 /pmc/articles/PMC6534167/ /pubmed/30816068 http://dx.doi.org/10.1089/scd.2018.0230 Text en © Xia Huang et al. 2019; Published by Mary Ann Liebert, Inc. This Open Access article is distributed under the terms of the Creative Commons Attribution Noncommercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and the source are cited.
spellingShingle Original Research Reports
Huang, Xia
Wang, Feilong
Zhao, Chen
Yang, Sheng
Cheng, Qianyu
Tang, Yingying
Zhang, Fugui
Zhang, Yan
Luo, Wenping
Wang, Chao
Zhou, Pengfei
Kim, Stephanie
Zuo, Guowei
Hu, Ning
Li, Ruidong
He, Tong-chuan
Zhang, Hongmei
Dentinogenesis and Tooth-Alveolar Bone Complex Defects in BMP9/GDF2 Knockout Mice
title Dentinogenesis and Tooth-Alveolar Bone Complex Defects in BMP9/GDF2 Knockout Mice
title_full Dentinogenesis and Tooth-Alveolar Bone Complex Defects in BMP9/GDF2 Knockout Mice
title_fullStr Dentinogenesis and Tooth-Alveolar Bone Complex Defects in BMP9/GDF2 Knockout Mice
title_full_unstemmed Dentinogenesis and Tooth-Alveolar Bone Complex Defects in BMP9/GDF2 Knockout Mice
title_short Dentinogenesis and Tooth-Alveolar Bone Complex Defects in BMP9/GDF2 Knockout Mice
title_sort dentinogenesis and tooth-alveolar bone complex defects in bmp9/gdf2 knockout mice
topic Original Research Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6534167/
https://www.ncbi.nlm.nih.gov/pubmed/30816068
http://dx.doi.org/10.1089/scd.2018.0230
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