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Bioinspired drug-delivery system emulating the natural bone healing cascade for diabetic periodontal bone regeneration

Diabetes mellitus (DM) aggravates periodontitis, resulting in accelerated periodontal bone resorption. Disordered glucose metabolism in DM causes reactive oxygen species (ROS) overproduction resulting in compromised bone healing, which makes diabetic periodontal bone regeneration a major challenge....

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Detalles Bibliográficos
Autores principales: Wang, He, Chang, Xiaowei, Ma, Qian, Sun, Boyang, Li, Han, Zhou, Jinmin, Hu, Yiyao, Yang, Xiaoyu, Li, Jie, Chen, Xin, Song, Jinlin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: KeAi Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9483739/
https://www.ncbi.nlm.nih.gov/pubmed/36185747
http://dx.doi.org/10.1016/j.bioactmat.2022.08.029
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author Wang, He
Chang, Xiaowei
Ma, Qian
Sun, Boyang
Li, Han
Zhou, Jinmin
Hu, Yiyao
Yang, Xiaoyu
Li, Jie
Chen, Xin
Song, Jinlin
author_facet Wang, He
Chang, Xiaowei
Ma, Qian
Sun, Boyang
Li, Han
Zhou, Jinmin
Hu, Yiyao
Yang, Xiaoyu
Li, Jie
Chen, Xin
Song, Jinlin
author_sort Wang, He
collection PubMed
description Diabetes mellitus (DM) aggravates periodontitis, resulting in accelerated periodontal bone resorption. Disordered glucose metabolism in DM causes reactive oxygen species (ROS) overproduction resulting in compromised bone healing, which makes diabetic periodontal bone regeneration a major challenge. Inspired by the natural bone healing cascade, a mesoporous silica nanoparticle (MSN)-incorporated PDLLA (poly(dl-lactide))-PEG-PDLLA (PPP) thermosensitive hydrogel with stepwise cargo release is designed to emulate the mesenchymal stem cell “recruitment-osteogenesis” cascade for diabetic periodontal bone regeneration. During therapy, SDF-1 quickly escapes from the hydrogel due to diffusion for early rat bone marrow stem cell (rBMSC) recruitment. Simultaneously, slow degradation of the hydrogel starts to gradually expose the MSNs for sustained release of metformin, which can scavenge the overproduced ROS under high glucose conditions to reverse the inhibited osteogenesis of rBMSCs by reactivating the AMPK/β-catenin pathway, resulting in regulation of the diabetic microenvironment and facilitation of osteogenesis. In vitro experiments indicate that the hydrogel markedly restores the inhibited migration and osteogenic capacities of rBMSCs under high glucose conditions. In vivo results suggest that it can effectively recruit rBMSCs to the periodontal defect and significantly promote periodontal bone regeneration under type 2 DM. In conclusion, our work provides a novel therapeutic strategy of a bioinspired drug-delivery system emulating the natural bone healing cascade for diabetic periodontal bone regeneration.
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spelling pubmed-94837392022-09-30 Bioinspired drug-delivery system emulating the natural bone healing cascade for diabetic periodontal bone regeneration Wang, He Chang, Xiaowei Ma, Qian Sun, Boyang Li, Han Zhou, Jinmin Hu, Yiyao Yang, Xiaoyu Li, Jie Chen, Xin Song, Jinlin Bioact Mater Article Diabetes mellitus (DM) aggravates periodontitis, resulting in accelerated periodontal bone resorption. Disordered glucose metabolism in DM causes reactive oxygen species (ROS) overproduction resulting in compromised bone healing, which makes diabetic periodontal bone regeneration a major challenge. Inspired by the natural bone healing cascade, a mesoporous silica nanoparticle (MSN)-incorporated PDLLA (poly(dl-lactide))-PEG-PDLLA (PPP) thermosensitive hydrogel with stepwise cargo release is designed to emulate the mesenchymal stem cell “recruitment-osteogenesis” cascade for diabetic periodontal bone regeneration. During therapy, SDF-1 quickly escapes from the hydrogel due to diffusion for early rat bone marrow stem cell (rBMSC) recruitment. Simultaneously, slow degradation of the hydrogel starts to gradually expose the MSNs for sustained release of metformin, which can scavenge the overproduced ROS under high glucose conditions to reverse the inhibited osteogenesis of rBMSCs by reactivating the AMPK/β-catenin pathway, resulting in regulation of the diabetic microenvironment and facilitation of osteogenesis. In vitro experiments indicate that the hydrogel markedly restores the inhibited migration and osteogenic capacities of rBMSCs under high glucose conditions. In vivo results suggest that it can effectively recruit rBMSCs to the periodontal defect and significantly promote periodontal bone regeneration under type 2 DM. In conclusion, our work provides a novel therapeutic strategy of a bioinspired drug-delivery system emulating the natural bone healing cascade for diabetic periodontal bone regeneration. KeAi Publishing 2022-09-14 /pmc/articles/PMC9483739/ /pubmed/36185747 http://dx.doi.org/10.1016/j.bioactmat.2022.08.029 Text en © 2022 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
Wang, He
Chang, Xiaowei
Ma, Qian
Sun, Boyang
Li, Han
Zhou, Jinmin
Hu, Yiyao
Yang, Xiaoyu
Li, Jie
Chen, Xin
Song, Jinlin
Bioinspired drug-delivery system emulating the natural bone healing cascade for diabetic periodontal bone regeneration
title Bioinspired drug-delivery system emulating the natural bone healing cascade for diabetic periodontal bone regeneration
title_full Bioinspired drug-delivery system emulating the natural bone healing cascade for diabetic periodontal bone regeneration
title_fullStr Bioinspired drug-delivery system emulating the natural bone healing cascade for diabetic periodontal bone regeneration
title_full_unstemmed Bioinspired drug-delivery system emulating the natural bone healing cascade for diabetic periodontal bone regeneration
title_short Bioinspired drug-delivery system emulating the natural bone healing cascade for diabetic periodontal bone regeneration
title_sort bioinspired drug-delivery system emulating the natural bone healing cascade for diabetic periodontal bone regeneration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9483739/
https://www.ncbi.nlm.nih.gov/pubmed/36185747
http://dx.doi.org/10.1016/j.bioactmat.2022.08.029
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