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In vitro evaluation of periapical lesion‐derived stem cells for dental pulp tissue engineering

Dental pulp tissue engineering is a promising alternative treatment for pulpitis and periapical periodontitis, and dental pulp stem cells (DPSCs) are considered to be the gold standard for dental seed cell research. Periapical lesions harbor mesenchymal stem cells with the capacity for self‐renewal...

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Autores principales: Li, Weiping, Mao, Mengying, Hu, Nan, Wang, Jia, Huang, Jing, Gu, Shensheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8727956/
https://www.ncbi.nlm.nih.gov/pubmed/34826215
http://dx.doi.org/10.1002/2211-5463.13336
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author Li, Weiping
Mao, Mengying
Hu, Nan
Wang, Jia
Huang, Jing
Gu, Shensheng
author_facet Li, Weiping
Mao, Mengying
Hu, Nan
Wang, Jia
Huang, Jing
Gu, Shensheng
author_sort Li, Weiping
collection PubMed
description Dental pulp tissue engineering is a promising alternative treatment for pulpitis and periapical periodontitis, and dental pulp stem cells (DPSCs) are considered to be the gold standard for dental seed cell research. Periapical lesions harbor mesenchymal stem cells with the capacity for self‐renewal and multilineage differentiation. However, it remains unknown whether these periapical lesion‐derived stem cells (PLDSCs) are suitable for dental pulp tissue engineering. To investigate this possibility, PLDSCs and DPSCs were isolated using the tissue outgrowth method and cultured under identical conditions. We then performed in vitro experiments to investigate their biological characteristics. Our results indicate that PLDSCs proliferate actively in vitro and exhibit similar morphology, immunophenotype and multilineage differentiation ability as DPSCs. Simultaneously, PLDSCs exhibit stronger migrative ability and express more vascular endothelial growth factor and glial cell line‐derived neurotrophic factor than DPSCs, and PLDSC‐derived conditioned medium was more effective in tube formation assay. The mRNA expression levels of immunomodulatory genes HLA‐G, IDO and ICAM‐1 were also higher in PLDSCs. However, regarding osteo/odontogenic differentiation, PLDSCs showed weaker alkaline phosphatase staining and lower calcified nodule formation compared to DPSCs, as well as lower expression of ALP, RUNX2 and DSPP, as confirmed by a quantitative RT‐PCR. The osteo/odontogenic protein expression levels of DSPP, RUNX2, DMP1 and SP7 were also higher in DPSCs. The present study demonstrates that PLDSCs demonstrate potential use as seed cells for dental pulp regeneration, especially for achieving enhanced neurovascularization.
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spelling pubmed-87279562022-01-11 In vitro evaluation of periapical lesion‐derived stem cells for dental pulp tissue engineering Li, Weiping Mao, Mengying Hu, Nan Wang, Jia Huang, Jing Gu, Shensheng FEBS Open Bio Research Articles Dental pulp tissue engineering is a promising alternative treatment for pulpitis and periapical periodontitis, and dental pulp stem cells (DPSCs) are considered to be the gold standard for dental seed cell research. Periapical lesions harbor mesenchymal stem cells with the capacity for self‐renewal and multilineage differentiation. However, it remains unknown whether these periapical lesion‐derived stem cells (PLDSCs) are suitable for dental pulp tissue engineering. To investigate this possibility, PLDSCs and DPSCs were isolated using the tissue outgrowth method and cultured under identical conditions. We then performed in vitro experiments to investigate their biological characteristics. Our results indicate that PLDSCs proliferate actively in vitro and exhibit similar morphology, immunophenotype and multilineage differentiation ability as DPSCs. Simultaneously, PLDSCs exhibit stronger migrative ability and express more vascular endothelial growth factor and glial cell line‐derived neurotrophic factor than DPSCs, and PLDSC‐derived conditioned medium was more effective in tube formation assay. The mRNA expression levels of immunomodulatory genes HLA‐G, IDO and ICAM‐1 were also higher in PLDSCs. However, regarding osteo/odontogenic differentiation, PLDSCs showed weaker alkaline phosphatase staining and lower calcified nodule formation compared to DPSCs, as well as lower expression of ALP, RUNX2 and DSPP, as confirmed by a quantitative RT‐PCR. The osteo/odontogenic protein expression levels of DSPP, RUNX2, DMP1 and SP7 were also higher in DPSCs. The present study demonstrates that PLDSCs demonstrate potential use as seed cells for dental pulp regeneration, especially for achieving enhanced neurovascularization. John Wiley and Sons Inc. 2021-12-05 /pmc/articles/PMC8727956/ /pubmed/34826215 http://dx.doi.org/10.1002/2211-5463.13336 Text en © 2021 The Authors. FEBS Open Bio published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Li, Weiping
Mao, Mengying
Hu, Nan
Wang, Jia
Huang, Jing
Gu, Shensheng
In vitro evaluation of periapical lesion‐derived stem cells for dental pulp tissue engineering
title In vitro evaluation of periapical lesion‐derived stem cells for dental pulp tissue engineering
title_full In vitro evaluation of periapical lesion‐derived stem cells for dental pulp tissue engineering
title_fullStr In vitro evaluation of periapical lesion‐derived stem cells for dental pulp tissue engineering
title_full_unstemmed In vitro evaluation of periapical lesion‐derived stem cells for dental pulp tissue engineering
title_short In vitro evaluation of periapical lesion‐derived stem cells for dental pulp tissue engineering
title_sort in vitro evaluation of periapical lesion‐derived stem cells for dental pulp tissue engineering
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8727956/
https://www.ncbi.nlm.nih.gov/pubmed/34826215
http://dx.doi.org/10.1002/2211-5463.13336
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