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Bio-clickable mussel-inspired peptides improve titanium-based material osseointegration synergistically with immunopolarization-regulation

Upon the osteoporotic condition, sluggish osteogenesis, excessive bone resorption, and chronic inflammation make the osseointegration of bioinert titanium (Ti) implants with surrounding bone tissues difficult, often lead to prosthesis loosening, bone collapse, and implant failure. In this study, we...

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Autores principales: Sun, Jie, Huang, Yingkang, Zhao, Huan, Niu, Junjie, Ling, Xuwei, Zhu, Can, Wang, Lin, Yang, Huilin, Yang, Zhilu, Pan, Guoqing, Shi, Qin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: KeAi Publishing 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8586442/
https://www.ncbi.nlm.nih.gov/pubmed/34820551
http://dx.doi.org/10.1016/j.bioactmat.2021.10.003
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author Sun, Jie
Huang, Yingkang
Zhao, Huan
Niu, Junjie
Ling, Xuwei
Zhu, Can
Wang, Lin
Yang, Huilin
Yang, Zhilu
Pan, Guoqing
Shi, Qin
author_facet Sun, Jie
Huang, Yingkang
Zhao, Huan
Niu, Junjie
Ling, Xuwei
Zhu, Can
Wang, Lin
Yang, Huilin
Yang, Zhilu
Pan, Guoqing
Shi, Qin
author_sort Sun, Jie
collection PubMed
description Upon the osteoporotic condition, sluggish osteogenesis, excessive bone resorption, and chronic inflammation make the osseointegration of bioinert titanium (Ti) implants with surrounding bone tissues difficult, often lead to prosthesis loosening, bone collapse, and implant failure. In this study, we firstly designed clickable mussel-inspired peptides (DOPA-N3) and grafted them onto the surfaces of Ti materials through robust catechol-TiO(2) coordinative interactions. Then, two dibenzylcyclooctyne (DBCO)-capped bioactive peptides RGD and BMP-2 bioactive domain (BMP-2) were clicked onto the DOPA-N3-coated Ti material surfaces via bio-orthogonal reaction. We characterized the surface morphology and biocompatibility of the Ti substrates and optimized the osteogenic capacity of Ti surfaces through adjusting the ideal ratios of BMP-2/RGD at 3:1. In vitro, the dual-functionalized Ti substrates exhibited excellent promotion on adhesion and osteogenesis of mesenchymal stem cells (MSCs), and conspicuous immunopolarization-regulation to shift macrophages to alternative (M2) phenotypes and inhibit inflammation, as well as enhancement of osseointegration and mechanical stability in osteoporotic rats. In summary, our biomimetic surface modification strategy by bio-orthogonal reaction provided a convenient and feasible method to resolve the bioinertia and clinical complications of Ti-based implants, which was conducive to the long-term success of Ti implants, especially in the osteoporotic or inflammatory conditions.
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spelling pubmed-85864422021-11-23 Bio-clickable mussel-inspired peptides improve titanium-based material osseointegration synergistically with immunopolarization-regulation Sun, Jie Huang, Yingkang Zhao, Huan Niu, Junjie Ling, Xuwei Zhu, Can Wang, Lin Yang, Huilin Yang, Zhilu Pan, Guoqing Shi, Qin Bioact Mater Article Upon the osteoporotic condition, sluggish osteogenesis, excessive bone resorption, and chronic inflammation make the osseointegration of bioinert titanium (Ti) implants with surrounding bone tissues difficult, often lead to prosthesis loosening, bone collapse, and implant failure. In this study, we firstly designed clickable mussel-inspired peptides (DOPA-N3) and grafted them onto the surfaces of Ti materials through robust catechol-TiO(2) coordinative interactions. Then, two dibenzylcyclooctyne (DBCO)-capped bioactive peptides RGD and BMP-2 bioactive domain (BMP-2) were clicked onto the DOPA-N3-coated Ti material surfaces via bio-orthogonal reaction. We characterized the surface morphology and biocompatibility of the Ti substrates and optimized the osteogenic capacity of Ti surfaces through adjusting the ideal ratios of BMP-2/RGD at 3:1. In vitro, the dual-functionalized Ti substrates exhibited excellent promotion on adhesion and osteogenesis of mesenchymal stem cells (MSCs), and conspicuous immunopolarization-regulation to shift macrophages to alternative (M2) phenotypes and inhibit inflammation, as well as enhancement of osseointegration and mechanical stability in osteoporotic rats. In summary, our biomimetic surface modification strategy by bio-orthogonal reaction provided a convenient and feasible method to resolve the bioinertia and clinical complications of Ti-based implants, which was conducive to the long-term success of Ti implants, especially in the osteoporotic or inflammatory conditions. KeAi Publishing 2021-10-07 /pmc/articles/PMC8586442/ /pubmed/34820551 http://dx.doi.org/10.1016/j.bioactmat.2021.10.003 Text en © 2021 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 Article
Sun, Jie
Huang, Yingkang
Zhao, Huan
Niu, Junjie
Ling, Xuwei
Zhu, Can
Wang, Lin
Yang, Huilin
Yang, Zhilu
Pan, Guoqing
Shi, Qin
Bio-clickable mussel-inspired peptides improve titanium-based material osseointegration synergistically with immunopolarization-regulation
title Bio-clickable mussel-inspired peptides improve titanium-based material osseointegration synergistically with immunopolarization-regulation
title_full Bio-clickable mussel-inspired peptides improve titanium-based material osseointegration synergistically with immunopolarization-regulation
title_fullStr Bio-clickable mussel-inspired peptides improve titanium-based material osseointegration synergistically with immunopolarization-regulation
title_full_unstemmed Bio-clickable mussel-inspired peptides improve titanium-based material osseointegration synergistically with immunopolarization-regulation
title_short Bio-clickable mussel-inspired peptides improve titanium-based material osseointegration synergistically with immunopolarization-regulation
title_sort bio-clickable mussel-inspired peptides improve titanium-based material osseointegration synergistically with immunopolarization-regulation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8586442/
https://www.ncbi.nlm.nih.gov/pubmed/34820551
http://dx.doi.org/10.1016/j.bioactmat.2021.10.003
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