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Sustained zinc release in cooperation with CaP scaffold promoted bone regeneration via directing stem cell fate and triggering a pro-healing immune stimuli

Metal ions have been identified as important bone metabolism regulators and widely used in the field of bone tissue engineering, however their exact role during bone regeneration remains unclear. Herein, the aim of study was to comprehensively explore the interactions between osteoinductive and oste...

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Autores principales: Huang, Xin, Huang, Donghua, Zhu, Ting, Yu, Xiaohua, Xu, Kaicheng, Li, Hengyuan, Qu, Hao, Zhou, Zhiyuan, Cheng, Kui, Wen, Wenjian, Ye, Zhaoming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8274038/
https://www.ncbi.nlm.nih.gov/pubmed/34247649
http://dx.doi.org/10.1186/s12951-021-00956-8
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author Huang, Xin
Huang, Donghua
Zhu, Ting
Yu, Xiaohua
Xu, Kaicheng
Li, Hengyuan
Qu, Hao
Zhou, Zhiyuan
Cheng, Kui
Wen, Wenjian
Ye, Zhaoming
author_facet Huang, Xin
Huang, Donghua
Zhu, Ting
Yu, Xiaohua
Xu, Kaicheng
Li, Hengyuan
Qu, Hao
Zhou, Zhiyuan
Cheng, Kui
Wen, Wenjian
Ye, Zhaoming
author_sort Huang, Xin
collection PubMed
description Metal ions have been identified as important bone metabolism regulators and widely used in the field of bone tissue engineering, however their exact role during bone regeneration remains unclear. Herein, the aim of study was to comprehensively explore the interactions between osteoinductive and osteo-immunomodulatory properties of these metal ions. In particular, the osteoinductive role of zinc ions (Zn(2+)), as well as its interactions with local immune microenvironment during bone healing process, was investigated in this study using a sustained Zn(2+) delivery system incorporating Zn(2+) into β-tricalcium phosphate/poly(L-lactic acid) (TCP/PLLA) scaffolds. The presence of Zn(2+) largely enhanced osteogenic differentiation of periosteum-derived progenitor cells (PDPCs), which was coincident with increased transition from M1 to M2 macrophages (M[Formula: see text] s). We further confirmed that induction of M2 polarization by Zn(2+) was realized via PI3K/Akt/mTOR pathway, whereas marker molecules on this pathway were strictly regulated by the addition of Zn(2+). Synergically, this favorable immunomodulatory effect of Zn(2+) further improved the osteogenic differentiation of PDPCs induced by Zn(2+) in vitro. Consistently, the spontaneous osteogenesis and pro-healing osteoimmunomodulation of the scaffolds were thoroughly identified in vivo using a rat air pouch model and a calvarial critical-size defect model. Taken together, Zn(2+)-releasing bioactive ceramics could be ideal scaffolds in bone tissue engineering due to their reciprocal interactions between osteoinductive and immunomodulatory characteristics. Clarification of this synergic role of Zn(2+) during osteogenesis could pave the way to develop more sophisticated metal-ion based orthopedic therapeutic strategies. [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-021-00956-8.
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spelling pubmed-82740382021-07-13 Sustained zinc release in cooperation with CaP scaffold promoted bone regeneration via directing stem cell fate and triggering a pro-healing immune stimuli Huang, Xin Huang, Donghua Zhu, Ting Yu, Xiaohua Xu, Kaicheng Li, Hengyuan Qu, Hao Zhou, Zhiyuan Cheng, Kui Wen, Wenjian Ye, Zhaoming J Nanobiotechnology Research Metal ions have been identified as important bone metabolism regulators and widely used in the field of bone tissue engineering, however their exact role during bone regeneration remains unclear. Herein, the aim of study was to comprehensively explore the interactions between osteoinductive and osteo-immunomodulatory properties of these metal ions. In particular, the osteoinductive role of zinc ions (Zn(2+)), as well as its interactions with local immune microenvironment during bone healing process, was investigated in this study using a sustained Zn(2+) delivery system incorporating Zn(2+) into β-tricalcium phosphate/poly(L-lactic acid) (TCP/PLLA) scaffolds. The presence of Zn(2+) largely enhanced osteogenic differentiation of periosteum-derived progenitor cells (PDPCs), which was coincident with increased transition from M1 to M2 macrophages (M[Formula: see text] s). We further confirmed that induction of M2 polarization by Zn(2+) was realized via PI3K/Akt/mTOR pathway, whereas marker molecules on this pathway were strictly regulated by the addition of Zn(2+). Synergically, this favorable immunomodulatory effect of Zn(2+) further improved the osteogenic differentiation of PDPCs induced by Zn(2+) in vitro. Consistently, the spontaneous osteogenesis and pro-healing osteoimmunomodulation of the scaffolds were thoroughly identified in vivo using a rat air pouch model and a calvarial critical-size defect model. Taken together, Zn(2+)-releasing bioactive ceramics could be ideal scaffolds in bone tissue engineering due to their reciprocal interactions between osteoinductive and immunomodulatory characteristics. Clarification of this synergic role of Zn(2+) during osteogenesis could pave the way to develop more sophisticated metal-ion based orthopedic therapeutic strategies. [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-021-00956-8. BioMed Central 2021-07-12 /pmc/articles/PMC8274038/ /pubmed/34247649 http://dx.doi.org/10.1186/s12951-021-00956-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Huang, Xin
Huang, Donghua
Zhu, Ting
Yu, Xiaohua
Xu, Kaicheng
Li, Hengyuan
Qu, Hao
Zhou, Zhiyuan
Cheng, Kui
Wen, Wenjian
Ye, Zhaoming
Sustained zinc release in cooperation with CaP scaffold promoted bone regeneration via directing stem cell fate and triggering a pro-healing immune stimuli
title Sustained zinc release in cooperation with CaP scaffold promoted bone regeneration via directing stem cell fate and triggering a pro-healing immune stimuli
title_full Sustained zinc release in cooperation with CaP scaffold promoted bone regeneration via directing stem cell fate and triggering a pro-healing immune stimuli
title_fullStr Sustained zinc release in cooperation with CaP scaffold promoted bone regeneration via directing stem cell fate and triggering a pro-healing immune stimuli
title_full_unstemmed Sustained zinc release in cooperation with CaP scaffold promoted bone regeneration via directing stem cell fate and triggering a pro-healing immune stimuli
title_short Sustained zinc release in cooperation with CaP scaffold promoted bone regeneration via directing stem cell fate and triggering a pro-healing immune stimuli
title_sort sustained zinc release in cooperation with cap scaffold promoted bone regeneration via directing stem cell fate and triggering a pro-healing immune stimuli
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8274038/
https://www.ncbi.nlm.nih.gov/pubmed/34247649
http://dx.doi.org/10.1186/s12951-021-00956-8
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