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Metformin carbon nanodots promote odontoblastic differentiation of dental pulp stem cells by pathway of autophagy

Human dental pulp stem cells (hDPSCs) have been a focus of pulp regeneration research because of their excellent odontogenic potential and availability. Applying the odontoblastic differentiation of hDPSCs to tooth regeneration has been challenging. Metformin-based carbon nanodots (MCDs) were synthe...

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Autores principales: Lu, Jinjin, Li, Rui, Ni, Shilei, Xie, Yuandong, Liu, Xinchen, Zhang, Kai, Li, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9506707/
https://www.ncbi.nlm.nih.gov/pubmed/36159662
http://dx.doi.org/10.3389/fbioe.2022.1002291
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author Lu, Jinjin
Li, Rui
Ni, Shilei
Xie, Yuandong
Liu, Xinchen
Zhang, Kai
Li, Yi
author_facet Lu, Jinjin
Li, Rui
Ni, Shilei
Xie, Yuandong
Liu, Xinchen
Zhang, Kai
Li, Yi
author_sort Lu, Jinjin
collection PubMed
description Human dental pulp stem cells (hDPSCs) have been a focus of pulp regeneration research because of their excellent odontogenic potential and availability. Applying the odontoblastic differentiation of hDPSCs to tooth regeneration has been challenging. Metformin-based carbon nanodots (MCDs) were synthesized and characterized to investigate their effects in vitro on odontoblastic hDPSC differentiation and the underlying mechanism. MCDs were synthesized by a hydrothermal treatment method and characterized using transmission electron microscopy (TEM), Fourier transform infrared spectroscopy, and X-ray photoelectron spectroscopy. The biocompatibility and fluorescence properties of the MCDs in Dulbecco’s modified Eagle’s medium high-glucose culture medium and the in vitro odontogenic potential and related mechanism of the bioactive nanomaterial was explored. TEM images showed that MCDs were spherical in shape with a size of approximately 5.9 nm. MCDs showed biological safety in cell viability, apoptosis, and fluorescence labelling ability at a concentration up to 200 μg/ml in vitro. The presence of MCDs facilitated high-efficiency odontogenic differentiation of hDPSCs by promoting odontogenic gene and protein expression. Moreover, MCDs promoted odontoblastic hDPSC differentiation via autophagy. MCDs are capable of activating autophagy and enhancing the odontogenic differentiation of hDPSCs by upregulating odontoblast gene marker (DMP1, DSPP, RUNX2, and SP7) and protein (DSPP and DMP1) expression.
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spelling pubmed-95067072022-09-24 Metformin carbon nanodots promote odontoblastic differentiation of dental pulp stem cells by pathway of autophagy Lu, Jinjin Li, Rui Ni, Shilei Xie, Yuandong Liu, Xinchen Zhang, Kai Li, Yi Front Bioeng Biotechnol Bioengineering and Biotechnology Human dental pulp stem cells (hDPSCs) have been a focus of pulp regeneration research because of their excellent odontogenic potential and availability. Applying the odontoblastic differentiation of hDPSCs to tooth regeneration has been challenging. Metformin-based carbon nanodots (MCDs) were synthesized and characterized to investigate their effects in vitro on odontoblastic hDPSC differentiation and the underlying mechanism. MCDs were synthesized by a hydrothermal treatment method and characterized using transmission electron microscopy (TEM), Fourier transform infrared spectroscopy, and X-ray photoelectron spectroscopy. The biocompatibility and fluorescence properties of the MCDs in Dulbecco’s modified Eagle’s medium high-glucose culture medium and the in vitro odontogenic potential and related mechanism of the bioactive nanomaterial was explored. TEM images showed that MCDs were spherical in shape with a size of approximately 5.9 nm. MCDs showed biological safety in cell viability, apoptosis, and fluorescence labelling ability at a concentration up to 200 μg/ml in vitro. The presence of MCDs facilitated high-efficiency odontogenic differentiation of hDPSCs by promoting odontogenic gene and protein expression. Moreover, MCDs promoted odontoblastic hDPSC differentiation via autophagy. MCDs are capable of activating autophagy and enhancing the odontogenic differentiation of hDPSCs by upregulating odontoblast gene marker (DMP1, DSPP, RUNX2, and SP7) and protein (DSPP and DMP1) expression. Frontiers Media S.A. 2022-09-09 /pmc/articles/PMC9506707/ /pubmed/36159662 http://dx.doi.org/10.3389/fbioe.2022.1002291 Text en Copyright © 2022 Lu, Li, Ni, Xie, Liu, Zhang and Li. https://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
Lu, Jinjin
Li, Rui
Ni, Shilei
Xie, Yuandong
Liu, Xinchen
Zhang, Kai
Li, Yi
Metformin carbon nanodots promote odontoblastic differentiation of dental pulp stem cells by pathway of autophagy
title Metformin carbon nanodots promote odontoblastic differentiation of dental pulp stem cells by pathway of autophagy
title_full Metformin carbon nanodots promote odontoblastic differentiation of dental pulp stem cells by pathway of autophagy
title_fullStr Metformin carbon nanodots promote odontoblastic differentiation of dental pulp stem cells by pathway of autophagy
title_full_unstemmed Metformin carbon nanodots promote odontoblastic differentiation of dental pulp stem cells by pathway of autophagy
title_short Metformin carbon nanodots promote odontoblastic differentiation of dental pulp stem cells by pathway of autophagy
title_sort metformin carbon nanodots promote odontoblastic differentiation of dental pulp stem cells by pathway of autophagy
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9506707/
https://www.ncbi.nlm.nih.gov/pubmed/36159662
http://dx.doi.org/10.3389/fbioe.2022.1002291
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