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The role of osteomodulin on osteo/odontogenic differentiation in human dental pulp stem cells
BACKGROUND: Extracellular matrix secretion and odontoblastic differentiation in human dental pulp stem cells (hDPSCs) are the cellular bases for reparative dentinogenesis. Osteomodulin (OMD) is a member of the small leucine-rich proteoglycan family distributed in the extracellular matrix but little...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6341608/ https://www.ncbi.nlm.nih.gov/pubmed/30670012 http://dx.doi.org/10.1186/s12903-018-0680-6 |
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author | Lin, Wenzhen Gao, Li Jiang, Wenxin Niu, Chenguang Yuan, Keyong Hu, Xuchen Ma, Rui Huang, Zhengwei |
author_facet | Lin, Wenzhen Gao, Li Jiang, Wenxin Niu, Chenguang Yuan, Keyong Hu, Xuchen Ma, Rui Huang, Zhengwei |
author_sort | Lin, Wenzhen |
collection | PubMed |
description | BACKGROUND: Extracellular matrix secretion and odontoblastic differentiation in human dental pulp stem cells (hDPSCs) are the cellular bases for reparative dentinogenesis. Osteomodulin (OMD) is a member of the small leucine-rich proteoglycan family distributed in the extracellular matrix but little is known about its role in osteo/odontogenic differentiation. The objective of this study was to investigate the role of OMD during osteo/odontoblastic differentiation of hDPSCs. METHODS: hDPSCs were selected using immune-magnetic beads and their capability of multi-differentiation was identified. OMD knockdown was achieved using short hairpin RNA (shRNA) lentivirus and was confirmed by western blot. Gene expression was measured by real-time qPCR and osteo/odontoblastic differentiation of hDPSCs was determined by alizarin red S staining. RESULTS: Compared with uninduced cells, the transcription of OMD was up-regulated by 35-fold at the late stage of osteo/odontogenic differentiation. shRNA-mediated gene silencing of OMD decreased the expression of odontoblastic genes, such as alkaline phosphatase (ALP), dentin matrix acidic phosphoprotein 1 (DMP1) and dentin sialophosphoprotein (DSPP). Besides, knockdown of OMD attenuated the mineralized nodules formation induced by osteo/odontogenic medium. CONCLUSIONS: These results implied that OMD may play a pivotal role in modulating the osteo/odontoblastic differentiation of hDPSCs. |
format | Online Article Text |
id | pubmed-6341608 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-63416082019-01-24 The role of osteomodulin on osteo/odontogenic differentiation in human dental pulp stem cells Lin, Wenzhen Gao, Li Jiang, Wenxin Niu, Chenguang Yuan, Keyong Hu, Xuchen Ma, Rui Huang, Zhengwei BMC Oral Health Research Article BACKGROUND: Extracellular matrix secretion and odontoblastic differentiation in human dental pulp stem cells (hDPSCs) are the cellular bases for reparative dentinogenesis. Osteomodulin (OMD) is a member of the small leucine-rich proteoglycan family distributed in the extracellular matrix but little is known about its role in osteo/odontogenic differentiation. The objective of this study was to investigate the role of OMD during osteo/odontoblastic differentiation of hDPSCs. METHODS: hDPSCs were selected using immune-magnetic beads and their capability of multi-differentiation was identified. OMD knockdown was achieved using short hairpin RNA (shRNA) lentivirus and was confirmed by western blot. Gene expression was measured by real-time qPCR and osteo/odontoblastic differentiation of hDPSCs was determined by alizarin red S staining. RESULTS: Compared with uninduced cells, the transcription of OMD was up-regulated by 35-fold at the late stage of osteo/odontogenic differentiation. shRNA-mediated gene silencing of OMD decreased the expression of odontoblastic genes, such as alkaline phosphatase (ALP), dentin matrix acidic phosphoprotein 1 (DMP1) and dentin sialophosphoprotein (DSPP). Besides, knockdown of OMD attenuated the mineralized nodules formation induced by osteo/odontogenic medium. CONCLUSIONS: These results implied that OMD may play a pivotal role in modulating the osteo/odontoblastic differentiation of hDPSCs. BioMed Central 2019-01-22 /pmc/articles/PMC6341608/ /pubmed/30670012 http://dx.doi.org/10.1186/s12903-018-0680-6 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Lin, Wenzhen Gao, Li Jiang, Wenxin Niu, Chenguang Yuan, Keyong Hu, Xuchen Ma, Rui Huang, Zhengwei The role of osteomodulin on osteo/odontogenic differentiation in human dental pulp stem cells |
title | The role of osteomodulin on osteo/odontogenic differentiation in human dental pulp stem cells |
title_full | The role of osteomodulin on osteo/odontogenic differentiation in human dental pulp stem cells |
title_fullStr | The role of osteomodulin on osteo/odontogenic differentiation in human dental pulp stem cells |
title_full_unstemmed | The role of osteomodulin on osteo/odontogenic differentiation in human dental pulp stem cells |
title_short | The role of osteomodulin on osteo/odontogenic differentiation in human dental pulp stem cells |
title_sort | role of osteomodulin on osteo/odontogenic differentiation in human dental pulp stem cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6341608/ https://www.ncbi.nlm.nih.gov/pubmed/30670012 http://dx.doi.org/10.1186/s12903-018-0680-6 |
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