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3D printed Ti-5Cu alloy accelerates osteogenic differentiation of MC3T3-E1 cells by stimulating the M2 phenotype polarization of macrophages

Ti-5Cu alloy has been proved to have excellent mechanical properties and cell compatibility and has certain antibacterial properties due to the addition of Cu. However, there are few studies on the effects of Ti-5Cu alloy on macrophage polarization and immune-related bone formation. In this study, w...

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Autores principales: Zhao, Xin, Zhou, Xing, Sun, Hui, Shi, Huixin, Song, Yiping, Wang, Qiang, Zhang, Guangping, Xu, Dake
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9585254/
https://www.ncbi.nlm.nih.gov/pubmed/36275667
http://dx.doi.org/10.3389/fimmu.2022.1001526
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author Zhao, Xin
Zhou, Xing
Sun, Hui
Shi, Huixin
Song, Yiping
Wang, Qiang
Zhang, Guangping
Xu, Dake
author_facet Zhao, Xin
Zhou, Xing
Sun, Hui
Shi, Huixin
Song, Yiping
Wang, Qiang
Zhang, Guangping
Xu, Dake
author_sort Zhao, Xin
collection PubMed
description Ti-5Cu alloy has been proved to have excellent mechanical properties and cell compatibility and has certain antibacterial properties due to the addition of Cu. However, there are few studies on the effects of Ti-5Cu alloy on macrophage polarization and immune-related bone formation. In this study, we prepared Ti-5Cu alloy by three-dimensional printing technology and found that Ti-5Cu alloy presented a much smoother surface compared with Ti. In addition, the CCK-8 results indicated the Ti-5Cu alloy had no cytotoxicity to RAW264.7 cells by co-culture. The results of inductively coupled plasma mass spectrometry showed that the concentration of Cu(2+) was 0.133 mg/L after 7 days of co-culture, and the CCK-8 results proved that Cu(2+) had no cytotoxicity to RAW264.7 at this concentration. Then, we studied the effects of Ti-5Cu alloy on macrophage polarization; it was shown that the Ti-5Cu alloy is more prone to modulate the RAW264.7 polarization towards the M2 phenotype and the conditioned medium derived from Ti-5Cu alloy significantly promoted the proliferation and osteogenic differentiation of MC3T3-E1 cells. However, when the expression of Oncostatin M (OSM) gene of RAW264.7 was knocked down, the osteogenic differentiation of MC3T3-E1 cells was decreased. This suggests that the OSM secreted by RAW264.7 co-cultured with Ti-5Cu alloy could accelerate the osteogenic differentiation of MC3T3-E1 cells by acting on OSMR/gp130 receptors.
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spelling pubmed-95852542022-10-22 3D printed Ti-5Cu alloy accelerates osteogenic differentiation of MC3T3-E1 cells by stimulating the M2 phenotype polarization of macrophages Zhao, Xin Zhou, Xing Sun, Hui Shi, Huixin Song, Yiping Wang, Qiang Zhang, Guangping Xu, Dake Front Immunol Immunology Ti-5Cu alloy has been proved to have excellent mechanical properties and cell compatibility and has certain antibacterial properties due to the addition of Cu. However, there are few studies on the effects of Ti-5Cu alloy on macrophage polarization and immune-related bone formation. In this study, we prepared Ti-5Cu alloy by three-dimensional printing technology and found that Ti-5Cu alloy presented a much smoother surface compared with Ti. In addition, the CCK-8 results indicated the Ti-5Cu alloy had no cytotoxicity to RAW264.7 cells by co-culture. The results of inductively coupled plasma mass spectrometry showed that the concentration of Cu(2+) was 0.133 mg/L after 7 days of co-culture, and the CCK-8 results proved that Cu(2+) had no cytotoxicity to RAW264.7 at this concentration. Then, we studied the effects of Ti-5Cu alloy on macrophage polarization; it was shown that the Ti-5Cu alloy is more prone to modulate the RAW264.7 polarization towards the M2 phenotype and the conditioned medium derived from Ti-5Cu alloy significantly promoted the proliferation and osteogenic differentiation of MC3T3-E1 cells. However, when the expression of Oncostatin M (OSM) gene of RAW264.7 was knocked down, the osteogenic differentiation of MC3T3-E1 cells was decreased. This suggests that the OSM secreted by RAW264.7 co-cultured with Ti-5Cu alloy could accelerate the osteogenic differentiation of MC3T3-E1 cells by acting on OSMR/gp130 receptors. Frontiers Media S.A. 2022-10-07 /pmc/articles/PMC9585254/ /pubmed/36275667 http://dx.doi.org/10.3389/fimmu.2022.1001526 Text en Copyright © 2022 Zhao, Zhou, Sun, Shi, Song, Wang, Zhang and Xu 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 Immunology
Zhao, Xin
Zhou, Xing
Sun, Hui
Shi, Huixin
Song, Yiping
Wang, Qiang
Zhang, Guangping
Xu, Dake
3D printed Ti-5Cu alloy accelerates osteogenic differentiation of MC3T3-E1 cells by stimulating the M2 phenotype polarization of macrophages
title 3D printed Ti-5Cu alloy accelerates osteogenic differentiation of MC3T3-E1 cells by stimulating the M2 phenotype polarization of macrophages
title_full 3D printed Ti-5Cu alloy accelerates osteogenic differentiation of MC3T3-E1 cells by stimulating the M2 phenotype polarization of macrophages
title_fullStr 3D printed Ti-5Cu alloy accelerates osteogenic differentiation of MC3T3-E1 cells by stimulating the M2 phenotype polarization of macrophages
title_full_unstemmed 3D printed Ti-5Cu alloy accelerates osteogenic differentiation of MC3T3-E1 cells by stimulating the M2 phenotype polarization of macrophages
title_short 3D printed Ti-5Cu alloy accelerates osteogenic differentiation of MC3T3-E1 cells by stimulating the M2 phenotype polarization of macrophages
title_sort 3d printed ti-5cu alloy accelerates osteogenic differentiation of mc3t3-e1 cells by stimulating the m2 phenotype polarization of macrophages
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9585254/
https://www.ncbi.nlm.nih.gov/pubmed/36275667
http://dx.doi.org/10.3389/fimmu.2022.1001526
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