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Engineering immunomodulatory and osteoinductive implant surfaces via mussel adhesion-mediated ion coordination and molecular clicking

Immune response and new tissue formation are important aspects of tissue repair. However, only a single aspect is generally considered in previous biomedical interventions, and the synergistic effect is unclear. Here, a dual-effect coating with immobilized immunomodulatory metal ions (e.g., Zn(2+))...

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Autores principales: Wang, Tao, Bai, Jiaxiang, Lu, Min, Huang, Chenglong, Geng, Dechun, Chen, Gang, Wang, Lei, Qi, Jin, Cui, Wenguo, Deng, Lianfu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8748715/
https://www.ncbi.nlm.nih.gov/pubmed/35013289
http://dx.doi.org/10.1038/s41467-021-27816-1
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author Wang, Tao
Bai, Jiaxiang
Lu, Min
Huang, Chenglong
Geng, Dechun
Chen, Gang
Wang, Lei
Qi, Jin
Cui, Wenguo
Deng, Lianfu
author_facet Wang, Tao
Bai, Jiaxiang
Lu, Min
Huang, Chenglong
Geng, Dechun
Chen, Gang
Wang, Lei
Qi, Jin
Cui, Wenguo
Deng, Lianfu
author_sort Wang, Tao
collection PubMed
description Immune response and new tissue formation are important aspects of tissue repair. However, only a single aspect is generally considered in previous biomedical interventions, and the synergistic effect is unclear. Here, a dual-effect coating with immobilized immunomodulatory metal ions (e.g., Zn(2+)) and osteoinductive growth factors (e.g., BMP-2 peptide) is designed via mussel adhesion-mediated ion coordination and molecular clicking strategy. Compared to the bare TiO(2) group, Zn(2+) can increase M2 macrophage recruitment by up to 92.5% in vivo and upregulate the expression of M2 cytokine IL-10 by 84.5%; while the dual-effect of Zn(2+) and BMP-2 peptide can increase M2 macrophages recruitment by up to 124.7% in vivo and upregulate the expression of M2 cytokine IL-10 by 171%. These benefits eventually significantly enhance bone-implant mechanical fixation (203.3 N) and new bone ingrowth (82.1%) compared to the bare TiO(2) (98.6 N and 45.1%, respectively). Taken together, the dual-effect coating can be utilized to synergistically modulate the osteoimmune microenvironment at the bone-implant interface, enhancing bone regeneration for successful implantation.
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spelling pubmed-87487152022-01-20 Engineering immunomodulatory and osteoinductive implant surfaces via mussel adhesion-mediated ion coordination and molecular clicking Wang, Tao Bai, Jiaxiang Lu, Min Huang, Chenglong Geng, Dechun Chen, Gang Wang, Lei Qi, Jin Cui, Wenguo Deng, Lianfu Nat Commun Article Immune response and new tissue formation are important aspects of tissue repair. However, only a single aspect is generally considered in previous biomedical interventions, and the synergistic effect is unclear. Here, a dual-effect coating with immobilized immunomodulatory metal ions (e.g., Zn(2+)) and osteoinductive growth factors (e.g., BMP-2 peptide) is designed via mussel adhesion-mediated ion coordination and molecular clicking strategy. Compared to the bare TiO(2) group, Zn(2+) can increase M2 macrophage recruitment by up to 92.5% in vivo and upregulate the expression of M2 cytokine IL-10 by 84.5%; while the dual-effect of Zn(2+) and BMP-2 peptide can increase M2 macrophages recruitment by up to 124.7% in vivo and upregulate the expression of M2 cytokine IL-10 by 171%. These benefits eventually significantly enhance bone-implant mechanical fixation (203.3 N) and new bone ingrowth (82.1%) compared to the bare TiO(2) (98.6 N and 45.1%, respectively). Taken together, the dual-effect coating can be utilized to synergistically modulate the osteoimmune microenvironment at the bone-implant interface, enhancing bone regeneration for successful implantation. Nature Publishing Group UK 2022-01-10 /pmc/articles/PMC8748715/ /pubmed/35013289 http://dx.doi.org/10.1038/s41467-021-27816-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Wang, Tao
Bai, Jiaxiang
Lu, Min
Huang, Chenglong
Geng, Dechun
Chen, Gang
Wang, Lei
Qi, Jin
Cui, Wenguo
Deng, Lianfu
Engineering immunomodulatory and osteoinductive implant surfaces via mussel adhesion-mediated ion coordination and molecular clicking
title Engineering immunomodulatory and osteoinductive implant surfaces via mussel adhesion-mediated ion coordination and molecular clicking
title_full Engineering immunomodulatory and osteoinductive implant surfaces via mussel adhesion-mediated ion coordination and molecular clicking
title_fullStr Engineering immunomodulatory and osteoinductive implant surfaces via mussel adhesion-mediated ion coordination and molecular clicking
title_full_unstemmed Engineering immunomodulatory and osteoinductive implant surfaces via mussel adhesion-mediated ion coordination and molecular clicking
title_short Engineering immunomodulatory and osteoinductive implant surfaces via mussel adhesion-mediated ion coordination and molecular clicking
title_sort engineering immunomodulatory and osteoinductive implant surfaces via mussel adhesion-mediated ion coordination and molecular clicking
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8748715/
https://www.ncbi.nlm.nih.gov/pubmed/35013289
http://dx.doi.org/10.1038/s41467-021-27816-1
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