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Investigate the Odontogenic Differentiation and Dentin–Pulp Tissue Regeneration Potential of Neural Crest Cells

Stem cell-based developmental engineering has been considered as a promising strategy for tissue/organ regeneration. Tooth is formed by sequential reciprocal interactions between epithelium derived from surface ectoderm and mesenchymal cells derived from cranial neural crest. The neural crest cell i...

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Autores principales: Zhang, Maolin, Zhang, Xiaochen, Luo, Jiaxin, Yan, Ran, Niibe, Kunimichi, Egusa, Hiroshi, Zhang, Zhiyuan, Xie, Ming, Jiang, Xinquan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7290043/
https://www.ncbi.nlm.nih.gov/pubmed/32582651
http://dx.doi.org/10.3389/fbioe.2020.00475
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author Zhang, Maolin
Zhang, Xiaochen
Luo, Jiaxin
Yan, Ran
Niibe, Kunimichi
Egusa, Hiroshi
Zhang, Zhiyuan
Xie, Ming
Jiang, Xinquan
author_facet Zhang, Maolin
Zhang, Xiaochen
Luo, Jiaxin
Yan, Ran
Niibe, Kunimichi
Egusa, Hiroshi
Zhang, Zhiyuan
Xie, Ming
Jiang, Xinquan
author_sort Zhang, Maolin
collection PubMed
description Stem cell-based developmental engineering has been considered as a promising strategy for tissue/organ regeneration. Tooth is formed by sequential reciprocal interactions between epithelium derived from surface ectoderm and mesenchymal cells derived from cranial neural crest. The neural crest cell is an appealing cell source for tooth development and regeneration research. In this study, we investigated the odontogenic differentiation and dentin-pulp complex regeneration potential of neural crest cells. Our results showed that neural crest cells (O9-1 mouse cranial neural crest cell line) can sequentially differentiate into dentin matrix acidic phosphoprotein 1 (DMP-1)-positive odontoblasts within a developing tooth germ in vitro. Moreover, O9-1 cells and induced pluripotent stem cell (iPSC)-derived neural crest-like cells (iNCLCs) can form well-organized vascularized dentin-pulp complex when transplanted in vivo with tooth scaffold. Furthermore, both O9-1 cells and iNCLCs can be differentiated into odontoblast-like cells, positive staining with odontogenic-related markers DMP-1 and dentin sialophosphoprotein (DSPP), under odontogenic induction with the administration of bone morphogenetic protein 4 (BMP-4). These results demonstrated that neural crest cells, especially the unlimited iNCLCs, are a promising cell source for tooth development and dental tissue/tooth organ regeneration studies.
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spelling pubmed-72900432020-06-23 Investigate the Odontogenic Differentiation and Dentin–Pulp Tissue Regeneration Potential of Neural Crest Cells Zhang, Maolin Zhang, Xiaochen Luo, Jiaxin Yan, Ran Niibe, Kunimichi Egusa, Hiroshi Zhang, Zhiyuan Xie, Ming Jiang, Xinquan Front Bioeng Biotechnol Bioengineering and Biotechnology Stem cell-based developmental engineering has been considered as a promising strategy for tissue/organ regeneration. Tooth is formed by sequential reciprocal interactions between epithelium derived from surface ectoderm and mesenchymal cells derived from cranial neural crest. The neural crest cell is an appealing cell source for tooth development and regeneration research. In this study, we investigated the odontogenic differentiation and dentin-pulp complex regeneration potential of neural crest cells. Our results showed that neural crest cells (O9-1 mouse cranial neural crest cell line) can sequentially differentiate into dentin matrix acidic phosphoprotein 1 (DMP-1)-positive odontoblasts within a developing tooth germ in vitro. Moreover, O9-1 cells and induced pluripotent stem cell (iPSC)-derived neural crest-like cells (iNCLCs) can form well-organized vascularized dentin-pulp complex when transplanted in vivo with tooth scaffold. Furthermore, both O9-1 cells and iNCLCs can be differentiated into odontoblast-like cells, positive staining with odontogenic-related markers DMP-1 and dentin sialophosphoprotein (DSPP), under odontogenic induction with the administration of bone morphogenetic protein 4 (BMP-4). These results demonstrated that neural crest cells, especially the unlimited iNCLCs, are a promising cell source for tooth development and dental tissue/tooth organ regeneration studies. Frontiers Media S.A. 2020-06-05 /pmc/articles/PMC7290043/ /pubmed/32582651 http://dx.doi.org/10.3389/fbioe.2020.00475 Text en Copyright © 2020 Zhang, Zhang, Luo, Yan, Niibe, Egusa, Zhang, Xie and Jiang. 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 Bioengineering and Biotechnology
Zhang, Maolin
Zhang, Xiaochen
Luo, Jiaxin
Yan, Ran
Niibe, Kunimichi
Egusa, Hiroshi
Zhang, Zhiyuan
Xie, Ming
Jiang, Xinquan
Investigate the Odontogenic Differentiation and Dentin–Pulp Tissue Regeneration Potential of Neural Crest Cells
title Investigate the Odontogenic Differentiation and Dentin–Pulp Tissue Regeneration Potential of Neural Crest Cells
title_full Investigate the Odontogenic Differentiation and Dentin–Pulp Tissue Regeneration Potential of Neural Crest Cells
title_fullStr Investigate the Odontogenic Differentiation and Dentin–Pulp Tissue Regeneration Potential of Neural Crest Cells
title_full_unstemmed Investigate the Odontogenic Differentiation and Dentin–Pulp Tissue Regeneration Potential of Neural Crest Cells
title_short Investigate the Odontogenic Differentiation and Dentin–Pulp Tissue Regeneration Potential of Neural Crest Cells
title_sort investigate the odontogenic differentiation and dentin–pulp tissue regeneration potential of neural crest cells
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7290043/
https://www.ncbi.nlm.nih.gov/pubmed/32582651
http://dx.doi.org/10.3389/fbioe.2020.00475
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