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Photothermal-Controlled Release of IL-4 in IL-4/PDA-Immobilized Black Titanium Dioxide (TiO(2)) Nanotubes Surface to Enhance Osseointegration: An In Vivo Study

Host immune response has gradually been accepted as a critical factor in achieving successful implant osseointegration. The aim of this study is to create a favorable immune microenvironment by the dominant release of IL-4 during the initial few days after implant insertion to mitigate early inflamm...

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Autores principales: Chen, Bo, Liang, Yu, Song, Yunjia, Liang, Yunkai, Jiao, Jian, Bai, Hong, Li, Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9457063/
https://www.ncbi.nlm.nih.gov/pubmed/36079344
http://dx.doi.org/10.3390/ma15175962
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author Chen, Bo
Liang, Yu
Song, Yunjia
Liang, Yunkai
Jiao, Jian
Bai, Hong
Li, Ying
author_facet Chen, Bo
Liang, Yu
Song, Yunjia
Liang, Yunkai
Jiao, Jian
Bai, Hong
Li, Ying
author_sort Chen, Bo
collection PubMed
description Host immune response has gradually been accepted as a critical factor in achieving successful implant osseointegration. The aim of this study is to create a favorable immune microenvironment by the dominant release of IL-4 during the initial few days after implant insertion to mitigate early inflammatory reactions and facilitate osseointegration. Herein, the B-TNT/PDA/IL-4 substrate was established by immobilizing an interleukin-4 (IL-4)/polydopamine (PDA) coating on a black TiO(2) nanotube (B-TNT) surface, achieving on-demand IL-4 release under near infrared (NIR) irradiation. Gene Ontology (GO) enrichment analyses based on high-throughput DNA microarray data revealed that IL-4 addition inhibited osteoclast differentiation and function. Animal experiment results suggested that the B-TNT/PDA/IL-4+Laser substrate induced the least inflammatory, tartrate-resistant acid phosphatase, inducible nitric oxide synthase and the most CD163 positive cells, compared to the Ti group at 7 days post-implantation. In addition, 28 days post-implantation, micro-computed tomography results showed the highest bone volume/total volume, trabecular thickness, trabecular number and the lowest trabecular separation, while Hematoxylin-eosin and Masson-trichrome staining revealed the largest amount of new bone formation for the B-TNT/PDA/IL-4+Laser group. This study revealed the osteoimmunoregulatory function of the novel B-TNT/PDA/IL-4 surface by photothermal release of IL-4 at an early period post-implantation, thus paving a new way for dental implant surface modification.
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spelling pubmed-94570632022-09-09 Photothermal-Controlled Release of IL-4 in IL-4/PDA-Immobilized Black Titanium Dioxide (TiO(2)) Nanotubes Surface to Enhance Osseointegration: An In Vivo Study Chen, Bo Liang, Yu Song, Yunjia Liang, Yunkai Jiao, Jian Bai, Hong Li, Ying Materials (Basel) Article Host immune response has gradually been accepted as a critical factor in achieving successful implant osseointegration. The aim of this study is to create a favorable immune microenvironment by the dominant release of IL-4 during the initial few days after implant insertion to mitigate early inflammatory reactions and facilitate osseointegration. Herein, the B-TNT/PDA/IL-4 substrate was established by immobilizing an interleukin-4 (IL-4)/polydopamine (PDA) coating on a black TiO(2) nanotube (B-TNT) surface, achieving on-demand IL-4 release under near infrared (NIR) irradiation. Gene Ontology (GO) enrichment analyses based on high-throughput DNA microarray data revealed that IL-4 addition inhibited osteoclast differentiation and function. Animal experiment results suggested that the B-TNT/PDA/IL-4+Laser substrate induced the least inflammatory, tartrate-resistant acid phosphatase, inducible nitric oxide synthase and the most CD163 positive cells, compared to the Ti group at 7 days post-implantation. In addition, 28 days post-implantation, micro-computed tomography results showed the highest bone volume/total volume, trabecular thickness, trabecular number and the lowest trabecular separation, while Hematoxylin-eosin and Masson-trichrome staining revealed the largest amount of new bone formation for the B-TNT/PDA/IL-4+Laser group. This study revealed the osteoimmunoregulatory function of the novel B-TNT/PDA/IL-4 surface by photothermal release of IL-4 at an early period post-implantation, thus paving a new way for dental implant surface modification. MDPI 2022-08-29 /pmc/articles/PMC9457063/ /pubmed/36079344 http://dx.doi.org/10.3390/ma15175962 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Chen, Bo
Liang, Yu
Song, Yunjia
Liang, Yunkai
Jiao, Jian
Bai, Hong
Li, Ying
Photothermal-Controlled Release of IL-4 in IL-4/PDA-Immobilized Black Titanium Dioxide (TiO(2)) Nanotubes Surface to Enhance Osseointegration: An In Vivo Study
title Photothermal-Controlled Release of IL-4 in IL-4/PDA-Immobilized Black Titanium Dioxide (TiO(2)) Nanotubes Surface to Enhance Osseointegration: An In Vivo Study
title_full Photothermal-Controlled Release of IL-4 in IL-4/PDA-Immobilized Black Titanium Dioxide (TiO(2)) Nanotubes Surface to Enhance Osseointegration: An In Vivo Study
title_fullStr Photothermal-Controlled Release of IL-4 in IL-4/PDA-Immobilized Black Titanium Dioxide (TiO(2)) Nanotubes Surface to Enhance Osseointegration: An In Vivo Study
title_full_unstemmed Photothermal-Controlled Release of IL-4 in IL-4/PDA-Immobilized Black Titanium Dioxide (TiO(2)) Nanotubes Surface to Enhance Osseointegration: An In Vivo Study
title_short Photothermal-Controlled Release of IL-4 in IL-4/PDA-Immobilized Black Titanium Dioxide (TiO(2)) Nanotubes Surface to Enhance Osseointegration: An In Vivo Study
title_sort photothermal-controlled release of il-4 in il-4/pda-immobilized black titanium dioxide (tio(2)) nanotubes surface to enhance osseointegration: an in vivo study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9457063/
https://www.ncbi.nlm.nih.gov/pubmed/36079344
http://dx.doi.org/10.3390/ma15175962
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