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A graphene oxide-loaded processed pyritum composite hydrogel for accelerated bone regeneration via mediation of M2 macrophage polarization
A coordinated interaction between osteogenesis and the osteoimmune microenvironment plays a vital role in regulating bone healing. However, disturbances in the pro- and anti-inflammatory balance hinder the therapeutic advantages of biomaterials. In this study, a novel composite hydrogel was successf...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10430169/ https://www.ncbi.nlm.nih.gov/pubmed/37593216 http://dx.doi.org/10.1016/j.mtbio.2023.100753 |
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author | Shi, Changcan Yu, Yinting Wu, Hongjuan Liu, Huanjin Guo, Mengyu Wang, Wenxin Wang, Dan Wei, Chenxu Zhai, Hao Yan, Guojun Chen, Zhipeng Cai, Ting Li, Weidong |
author_facet | Shi, Changcan Yu, Yinting Wu, Hongjuan Liu, Huanjin Guo, Mengyu Wang, Wenxin Wang, Dan Wei, Chenxu Zhai, Hao Yan, Guojun Chen, Zhipeng Cai, Ting Li, Weidong |
author_sort | Shi, Changcan |
collection | PubMed |
description | A coordinated interaction between osteogenesis and the osteoimmune microenvironment plays a vital role in regulating bone healing. However, disturbances in the pro- and anti-inflammatory balance hinder the therapeutic advantages of biomaterials. In this study, a novel composite hydrogel was successfully fabricated using graphene oxide (GO)-loaded processed pyritum (PP) in combination with poly(ethylene glycol) diacrylate (PEGDA) and carboxymethyl chitosan (CMC). Subsequently, the immunomodulatory effects and bone regenerative potential of PP/GO@PEGDA/CMC were investigated. The results demonstrated that the PP/GO@PEGDA/CMC hydrogel possessed excellent mechanical properties, swelling capacity, and stability. Moreover, PP/GO@PEGDA/CMC prominently promoted M2 polarization and increased the levels of anti-inflammatory factors (interleukin (IL)-4, IL-10, and transforming growth factor-β). These beneficial effects facilitated the proliferation and osteogenic differentiation of bone marrow mesenchymal stem cells in vitro. Additionally, the in vivo results further verified that the implantation of PP/GO@PEGDA/CMC markedly reduced local inflammation while enhancing bone regeneration at 8 weeks post-implantation. Therefore, the results of this study provide potential therapeutic strategies for bone tissue repair and regeneration by modulating the immune microenvironment. |
format | Online Article Text |
id | pubmed-10430169 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-104301692023-08-17 A graphene oxide-loaded processed pyritum composite hydrogel for accelerated bone regeneration via mediation of M2 macrophage polarization Shi, Changcan Yu, Yinting Wu, Hongjuan Liu, Huanjin Guo, Mengyu Wang, Wenxin Wang, Dan Wei, Chenxu Zhai, Hao Yan, Guojun Chen, Zhipeng Cai, Ting Li, Weidong Mater Today Bio Full Length Article A coordinated interaction between osteogenesis and the osteoimmune microenvironment plays a vital role in regulating bone healing. However, disturbances in the pro- and anti-inflammatory balance hinder the therapeutic advantages of biomaterials. In this study, a novel composite hydrogel was successfully fabricated using graphene oxide (GO)-loaded processed pyritum (PP) in combination with poly(ethylene glycol) diacrylate (PEGDA) and carboxymethyl chitosan (CMC). Subsequently, the immunomodulatory effects and bone regenerative potential of PP/GO@PEGDA/CMC were investigated. The results demonstrated that the PP/GO@PEGDA/CMC hydrogel possessed excellent mechanical properties, swelling capacity, and stability. Moreover, PP/GO@PEGDA/CMC prominently promoted M2 polarization and increased the levels of anti-inflammatory factors (interleukin (IL)-4, IL-10, and transforming growth factor-β). These beneficial effects facilitated the proliferation and osteogenic differentiation of bone marrow mesenchymal stem cells in vitro. Additionally, the in vivo results further verified that the implantation of PP/GO@PEGDA/CMC markedly reduced local inflammation while enhancing bone regeneration at 8 weeks post-implantation. Therefore, the results of this study provide potential therapeutic strategies for bone tissue repair and regeneration by modulating the immune microenvironment. Elsevier 2023-07-30 /pmc/articles/PMC10430169/ /pubmed/37593216 http://dx.doi.org/10.1016/j.mtbio.2023.100753 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Full Length Article Shi, Changcan Yu, Yinting Wu, Hongjuan Liu, Huanjin Guo, Mengyu Wang, Wenxin Wang, Dan Wei, Chenxu Zhai, Hao Yan, Guojun Chen, Zhipeng Cai, Ting Li, Weidong A graphene oxide-loaded processed pyritum composite hydrogel for accelerated bone regeneration via mediation of M2 macrophage polarization |
title | A graphene oxide-loaded processed pyritum composite hydrogel for accelerated bone regeneration via mediation of M2 macrophage polarization |
title_full | A graphene oxide-loaded processed pyritum composite hydrogel for accelerated bone regeneration via mediation of M2 macrophage polarization |
title_fullStr | A graphene oxide-loaded processed pyritum composite hydrogel for accelerated bone regeneration via mediation of M2 macrophage polarization |
title_full_unstemmed | A graphene oxide-loaded processed pyritum composite hydrogel for accelerated bone regeneration via mediation of M2 macrophage polarization |
title_short | A graphene oxide-loaded processed pyritum composite hydrogel for accelerated bone regeneration via mediation of M2 macrophage polarization |
title_sort | graphene oxide-loaded processed pyritum composite hydrogel for accelerated bone regeneration via mediation of m2 macrophage polarization |
topic | Full Length Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10430169/ https://www.ncbi.nlm.nih.gov/pubmed/37593216 http://dx.doi.org/10.1016/j.mtbio.2023.100753 |
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