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Injectable thermosensitive chitosan/gelatin hydrogel for dental pulp stem cells proliferation and differentiation

[Image: see text] Introduction: Biocompatible and biodegradable scaffolds based on natural polymers such as gelatin and chitosan (CS) provide suitable microenvironments in dental tissue engineering. In the present study, we report on the synthesis of injectable thermosensitive hydrogel (PNIPAAm-g-CS...

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Autores principales: Samiei, Mohammad, Dalir Abdollahinia, Elaheh, Amiryaghoubi, Nazanin, Fathi, Marziyeh, Barar, Jaleh, Omidi, Yadollah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tabriz University of Medical Sciences (TUOMS Publishing Group) 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9923811/
https://www.ncbi.nlm.nih.gov/pubmed/36816999
http://dx.doi.org/10.34172/bi.2022.23904
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author Samiei, Mohammad
Dalir Abdollahinia, Elaheh
Amiryaghoubi, Nazanin
Fathi, Marziyeh
Barar, Jaleh
Omidi, Yadollah
author_facet Samiei, Mohammad
Dalir Abdollahinia, Elaheh
Amiryaghoubi, Nazanin
Fathi, Marziyeh
Barar, Jaleh
Omidi, Yadollah
author_sort Samiei, Mohammad
collection PubMed
description [Image: see text] Introduction: Biocompatible and biodegradable scaffolds based on natural polymers such as gelatin and chitosan (CS) provide suitable microenvironments in dental tissue engineering. In the present study, we report on the synthesis of injectable thermosensitive hydrogel (PNIPAAm-g-CS copolymer/gelatin hybrid hydrogel) for osteogenic differentiation of human dental pulp stem cells (hDPSCs). Methods: The CS-g-PNIPAAm was synthesized using the reaction of carboxyl terminated PNIPAAm with CS, which was then mixed with various amounts of gelatin solution in the presence of genipin as a chemical crosslinker to gain a homogenous solution. The chemical composition and microstructures of the fabricated hydrogels were confirmed by FT-IR and SEM analysis, respectively. To evaluate the mechanical properties (e.g., storage and loss modulus of the gels), the rheological analysis was considered. Calcium deposition and ALP activity of DPSCs were carried out using alizarin red staining and ALP test. While the live/dead assay was performed to study its toxicity, the real-time PCR was conducted to investigate the osteogenic differentiation of hDPSCs cultured on prepared hydrogels. Results: The hydrogels with higher gelatin incorporation showed a slightly looser network compared to the other ones. The hydrogel with less gelatin indicates a rather higher value of G', indicating a higher elasticity due to more crosslinking reaction of amine groups of CS via a covalent bond with genipin. All the hydrogels contained viable cells with negligible dead cells, indicating the high biocompatibility of the prepared hydrogels for hDPSCs. The quantitative results of alizarin red staining displayed a significant rise in calcium deposition in hDPSCs cultured on prepared hydrogels after 21 days. Further, hDPSCs cultured on hydrogel with more gelatin displayed the most ALP activity. The expression of late osteogenic genes such as OCN and BMP-2 were respectively 6 and 4 times higher on the hydrogel with more gelatin than the control group after 21 days. Conclusion: The prepared PNIPAAm-g-CS copolymer/gelatin hybrid hydrogel presented great features (e.g., porous structure, suitable rheological behavior, and improved cell viability), and resulted in osteogenic differentiation necessary for dental tissue engineering.
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spelling pubmed-99238112023-02-16 Injectable thermosensitive chitosan/gelatin hydrogel for dental pulp stem cells proliferation and differentiation Samiei, Mohammad Dalir Abdollahinia, Elaheh Amiryaghoubi, Nazanin Fathi, Marziyeh Barar, Jaleh Omidi, Yadollah Bioimpacts Original Article [Image: see text] Introduction: Biocompatible and biodegradable scaffolds based on natural polymers such as gelatin and chitosan (CS) provide suitable microenvironments in dental tissue engineering. In the present study, we report on the synthesis of injectable thermosensitive hydrogel (PNIPAAm-g-CS copolymer/gelatin hybrid hydrogel) for osteogenic differentiation of human dental pulp stem cells (hDPSCs). Methods: The CS-g-PNIPAAm was synthesized using the reaction of carboxyl terminated PNIPAAm with CS, which was then mixed with various amounts of gelatin solution in the presence of genipin as a chemical crosslinker to gain a homogenous solution. The chemical composition and microstructures of the fabricated hydrogels were confirmed by FT-IR and SEM analysis, respectively. To evaluate the mechanical properties (e.g., storage and loss modulus of the gels), the rheological analysis was considered. Calcium deposition and ALP activity of DPSCs were carried out using alizarin red staining and ALP test. While the live/dead assay was performed to study its toxicity, the real-time PCR was conducted to investigate the osteogenic differentiation of hDPSCs cultured on prepared hydrogels. Results: The hydrogels with higher gelatin incorporation showed a slightly looser network compared to the other ones. The hydrogel with less gelatin indicates a rather higher value of G', indicating a higher elasticity due to more crosslinking reaction of amine groups of CS via a covalent bond with genipin. All the hydrogels contained viable cells with negligible dead cells, indicating the high biocompatibility of the prepared hydrogels for hDPSCs. The quantitative results of alizarin red staining displayed a significant rise in calcium deposition in hDPSCs cultured on prepared hydrogels after 21 days. Further, hDPSCs cultured on hydrogel with more gelatin displayed the most ALP activity. The expression of late osteogenic genes such as OCN and BMP-2 were respectively 6 and 4 times higher on the hydrogel with more gelatin than the control group after 21 days. Conclusion: The prepared PNIPAAm-g-CS copolymer/gelatin hybrid hydrogel presented great features (e.g., porous structure, suitable rheological behavior, and improved cell viability), and resulted in osteogenic differentiation necessary for dental tissue engineering. Tabriz University of Medical Sciences (TUOMS Publishing Group) 2023 2022-06-20 /pmc/articles/PMC9923811/ /pubmed/36816999 http://dx.doi.org/10.34172/bi.2022.23904 Text en © 2023 The Author(s). https://creativecommons.org/licenses/by-nc/4.0/This work is published by BioImpacts as an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ). Non-commercial uses of the work are permitted, provided the original work is properly cited.
spellingShingle Original Article
Samiei, Mohammad
Dalir Abdollahinia, Elaheh
Amiryaghoubi, Nazanin
Fathi, Marziyeh
Barar, Jaleh
Omidi, Yadollah
Injectable thermosensitive chitosan/gelatin hydrogel for dental pulp stem cells proliferation and differentiation
title Injectable thermosensitive chitosan/gelatin hydrogel for dental pulp stem cells proliferation and differentiation
title_full Injectable thermosensitive chitosan/gelatin hydrogel for dental pulp stem cells proliferation and differentiation
title_fullStr Injectable thermosensitive chitosan/gelatin hydrogel for dental pulp stem cells proliferation and differentiation
title_full_unstemmed Injectable thermosensitive chitosan/gelatin hydrogel for dental pulp stem cells proliferation and differentiation
title_short Injectable thermosensitive chitosan/gelatin hydrogel for dental pulp stem cells proliferation and differentiation
title_sort injectable thermosensitive chitosan/gelatin hydrogel for dental pulp stem cells proliferation and differentiation
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9923811/
https://www.ncbi.nlm.nih.gov/pubmed/36816999
http://dx.doi.org/10.34172/bi.2022.23904
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