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Effect of TNF-α on the proliferation and osteogenesis of human periodontal mesenchymal stem cells
The aim of the present study was to investigate the effect of tumor necrosis factor-α (TNF-α) on the proliferation and osteogenesis of human periodontal mesenchymal stem cells (hPDLSCs). Antigen expression in hPDLSCs was detected by flow cytometry. hPDLSCs were divided into four groups: A control gr...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7967876/ https://www.ncbi.nlm.nih.gov/pubmed/33747173 http://dx.doi.org/10.3892/etm.2021.9851 |
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author | Cao, Yiting Wang, Yiwei Li, Chenlin Jiang, Qian Zhu, Laikuan |
author_facet | Cao, Yiting Wang, Yiwei Li, Chenlin Jiang, Qian Zhu, Laikuan |
author_sort | Cao, Yiting |
collection | PubMed |
description | The aim of the present study was to investigate the effect of tumor necrosis factor-α (TNF-α) on the proliferation and osteogenesis of human periodontal mesenchymal stem cells (hPDLSCs). Antigen expression in hPDLSCs was detected by flow cytometry. hPDLSCs were divided into four groups: A control group with no TNF-α treatment, and three experimental groups treated with 0.1, 1 and 10 ng/ml TNF-α, respectively. The effect of TNF-α on proliferation of hPDLSCs in vitro was detected using a Cell Counting Kit-8 assay. Differentiation into an osteogenic lineage was detected by alkaline phosphatase sand alizarin red staining, and the mRNA and protein expression levels of runt-related transcription factor 2 (Runx2), osteocalcin (OCN) and type I collagen (Col-I) were detected using reverse transcription-quantitative PCR and western blot respectively. Following treatment with 10 ng/ml TNF-α, proliferation was significantly increased compared with an untreated control group (P<0.01). Additionally, there was a significant inhibition of alkaline phosphatase enzyme activity, alizarin red mineralization node size, and in the gene and protein expression levels of osteogenic differentiation markers, including Runx2, OCN and COL-I (all, P<0.05). Taken together, the results indicated that treatment with 10 ng/ml TNF-α promoted the proliferation of hPDLSCs in vitro and inhibited osteogenic differentiation of hPDLSCs, providing an experimental basis for regulation of hPDLSC-mediated periodontal tissue regeneration. |
format | Online Article Text |
id | pubmed-7967876 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-79678762021-03-19 Effect of TNF-α on the proliferation and osteogenesis of human periodontal mesenchymal stem cells Cao, Yiting Wang, Yiwei Li, Chenlin Jiang, Qian Zhu, Laikuan Exp Ther Med Articles The aim of the present study was to investigate the effect of tumor necrosis factor-α (TNF-α) on the proliferation and osteogenesis of human periodontal mesenchymal stem cells (hPDLSCs). Antigen expression in hPDLSCs was detected by flow cytometry. hPDLSCs were divided into four groups: A control group with no TNF-α treatment, and three experimental groups treated with 0.1, 1 and 10 ng/ml TNF-α, respectively. The effect of TNF-α on proliferation of hPDLSCs in vitro was detected using a Cell Counting Kit-8 assay. Differentiation into an osteogenic lineage was detected by alkaline phosphatase sand alizarin red staining, and the mRNA and protein expression levels of runt-related transcription factor 2 (Runx2), osteocalcin (OCN) and type I collagen (Col-I) were detected using reverse transcription-quantitative PCR and western blot respectively. Following treatment with 10 ng/ml TNF-α, proliferation was significantly increased compared with an untreated control group (P<0.01). Additionally, there was a significant inhibition of alkaline phosphatase enzyme activity, alizarin red mineralization node size, and in the gene and protein expression levels of osteogenic differentiation markers, including Runx2, OCN and COL-I (all, P<0.05). Taken together, the results indicated that treatment with 10 ng/ml TNF-α promoted the proliferation of hPDLSCs in vitro and inhibited osteogenic differentiation of hPDLSCs, providing an experimental basis for regulation of hPDLSC-mediated periodontal tissue regeneration. D.A. Spandidos 2021-05 2021-02-26 /pmc/articles/PMC7967876/ /pubmed/33747173 http://dx.doi.org/10.3892/etm.2021.9851 Text en Copyright: © Cao et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Cao, Yiting Wang, Yiwei Li, Chenlin Jiang, Qian Zhu, Laikuan Effect of TNF-α on the proliferation and osteogenesis of human periodontal mesenchymal stem cells |
title | Effect of TNF-α on the proliferation and osteogenesis of human periodontal mesenchymal stem cells |
title_full | Effect of TNF-α on the proliferation and osteogenesis of human periodontal mesenchymal stem cells |
title_fullStr | Effect of TNF-α on the proliferation and osteogenesis of human periodontal mesenchymal stem cells |
title_full_unstemmed | Effect of TNF-α on the proliferation and osteogenesis of human periodontal mesenchymal stem cells |
title_short | Effect of TNF-α on the proliferation and osteogenesis of human periodontal mesenchymal stem cells |
title_sort | effect of tnf-α on the proliferation and osteogenesis of human periodontal mesenchymal stem cells |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7967876/ https://www.ncbi.nlm.nih.gov/pubmed/33747173 http://dx.doi.org/10.3892/etm.2021.9851 |
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