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Dentin sialoprotein facilitates dental mesenchymal cell differentiation and dentin formation
Dentin sialoprotein (DSP) is a dentin extracellular matrix protein. It is involved in dental mesenchymal cell lineages and dentin formation through regulation of its target gene expression. DSP mutations cause dentin genetic diseases. However, mechanisms of DSP in controlling dental mesenchymal cell...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5428264/ https://www.ncbi.nlm.nih.gov/pubmed/28331230 http://dx.doi.org/10.1038/s41598-017-00339-w |
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author | Li, Wentong Chen, Lei Chen, Zhuo Wu, Lian Feng, Junsheng Wang, Feng Shoff, Lisa Li, Xin Donly, Kevin J. MacDougall, Mary Chen, Shuo |
author_facet | Li, Wentong Chen, Lei Chen, Zhuo Wu, Lian Feng, Junsheng Wang, Feng Shoff, Lisa Li, Xin Donly, Kevin J. MacDougall, Mary Chen, Shuo |
author_sort | Li, Wentong |
collection | PubMed |
description | Dentin sialoprotein (DSP) is a dentin extracellular matrix protein. It is involved in dental mesenchymal cell lineages and dentin formation through regulation of its target gene expression. DSP mutations cause dentin genetic diseases. However, mechanisms of DSP in controlling dental mesenchymal cell differentiation are unknown. Using DSP as bait, we screened a protein library from mouse odontoblastic cells and found that DSP is a ligand and binds to cell surface receptor, occludin. Further study identified that the C-terminal DSP domain(aa 363–458) interacts with the occludin extracellular loop 2(aa 194–241). The C-terminal DSP domain induced phosphorylation of occludin Ser(490) and focal adhesion kinase (FAK) Ser(722) and Tyr(576). Coexpression of DSP, occludin and FAK was detected in dental mesenchymal cells during tooth development. Occludin physically interacts with FAK, and occludin and FAK phosphorylation can be blocked by DSP and occludin antibodies. This DSP domain facilitates dental mesenchymal cell differentiation and mineralization. Furthermore, transplantation and pulp-capping procedures revealed that this DSP domain induces endogenous dental pulp mesenchymal cell proliferation, differentiation and migration, while stimulating blood vessel proliferation. This study elucidates the mechanism of DSP in dental mesenchymal lineages and implies that DSP may serve as a therapeutic agent for dentin-pulp complex regeneration in dental caries. |
format | Online Article Text |
id | pubmed-5428264 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54282642017-05-15 Dentin sialoprotein facilitates dental mesenchymal cell differentiation and dentin formation Li, Wentong Chen, Lei Chen, Zhuo Wu, Lian Feng, Junsheng Wang, Feng Shoff, Lisa Li, Xin Donly, Kevin J. MacDougall, Mary Chen, Shuo Sci Rep Article Dentin sialoprotein (DSP) is a dentin extracellular matrix protein. It is involved in dental mesenchymal cell lineages and dentin formation through regulation of its target gene expression. DSP mutations cause dentin genetic diseases. However, mechanisms of DSP in controlling dental mesenchymal cell differentiation are unknown. Using DSP as bait, we screened a protein library from mouse odontoblastic cells and found that DSP is a ligand and binds to cell surface receptor, occludin. Further study identified that the C-terminal DSP domain(aa 363–458) interacts with the occludin extracellular loop 2(aa 194–241). The C-terminal DSP domain induced phosphorylation of occludin Ser(490) and focal adhesion kinase (FAK) Ser(722) and Tyr(576). Coexpression of DSP, occludin and FAK was detected in dental mesenchymal cells during tooth development. Occludin physically interacts with FAK, and occludin and FAK phosphorylation can be blocked by DSP and occludin antibodies. This DSP domain facilitates dental mesenchymal cell differentiation and mineralization. Furthermore, transplantation and pulp-capping procedures revealed that this DSP domain induces endogenous dental pulp mesenchymal cell proliferation, differentiation and migration, while stimulating blood vessel proliferation. This study elucidates the mechanism of DSP in dental mesenchymal lineages and implies that DSP may serve as a therapeutic agent for dentin-pulp complex regeneration in dental caries. Nature Publishing Group UK 2017-03-22 /pmc/articles/PMC5428264/ /pubmed/28331230 http://dx.doi.org/10.1038/s41598-017-00339-w Text en © The Author(s) 2017 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 Li, Wentong Chen, Lei Chen, Zhuo Wu, Lian Feng, Junsheng Wang, Feng Shoff, Lisa Li, Xin Donly, Kevin J. MacDougall, Mary Chen, Shuo Dentin sialoprotein facilitates dental mesenchymal cell differentiation and dentin formation |
title | Dentin sialoprotein facilitates dental mesenchymal cell differentiation and dentin formation |
title_full | Dentin sialoprotein facilitates dental mesenchymal cell differentiation and dentin formation |
title_fullStr | Dentin sialoprotein facilitates dental mesenchymal cell differentiation and dentin formation |
title_full_unstemmed | Dentin sialoprotein facilitates dental mesenchymal cell differentiation and dentin formation |
title_short | Dentin sialoprotein facilitates dental mesenchymal cell differentiation and dentin formation |
title_sort | dentin sialoprotein facilitates dental mesenchymal cell differentiation and dentin formation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5428264/ https://www.ncbi.nlm.nih.gov/pubmed/28331230 http://dx.doi.org/10.1038/s41598-017-00339-w |
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