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Stepwise 3D-spatio-temporal magnesium cationic niche: Nanocomposite scaffold mediated microenvironment for modulating intramembranous ossification

The fate of cells and subsequent bone regeneration is highly correlated with temporospatial coordination of chemical, biological, or physical cues within a local tissue microenvironment. Deeper understanding of how mammalian cells react to local tissue microenvironment is paramount important when de...

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Autores principales: Shen, Jie, Chen, Bo, Zhai, Xinyun, Qiao, Wei, Wu, Shuilin, Liu, Xuanyong, Zhao, Ying, Ruan, Changshun, Pan, Haobo, Chu, Paul K., Cheung, Kenneth M.C., Yeung, Kelvin W.K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: KeAi Publishing 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7492774/
https://www.ncbi.nlm.nih.gov/pubmed/32995676
http://dx.doi.org/10.1016/j.bioactmat.2020.08.025
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author Shen, Jie
Chen, Bo
Zhai, Xinyun
Qiao, Wei
Wu, Shuilin
Liu, Xuanyong
Zhao, Ying
Ruan, Changshun
Pan, Haobo
Chu, Paul K.
Cheung, Kenneth M.C.
Yeung, Kelvin W.K.
author_facet Shen, Jie
Chen, Bo
Zhai, Xinyun
Qiao, Wei
Wu, Shuilin
Liu, Xuanyong
Zhao, Ying
Ruan, Changshun
Pan, Haobo
Chu, Paul K.
Cheung, Kenneth M.C.
Yeung, Kelvin W.K.
author_sort Shen, Jie
collection PubMed
description The fate of cells and subsequent bone regeneration is highly correlated with temporospatial coordination of chemical, biological, or physical cues within a local tissue microenvironment. Deeper understanding of how mammalian cells react to local tissue microenvironment is paramount important when designing next generation of biomaterials for tissue engineering. This study aims to investigate that the regulation of magnesium cationic (Mg(2+)) tissue microenvironment is able to convince early-stage bone regeneration and its mechanism undergoes intramembranous ossification. It was discovered that moderate Mg(2+) content niche (~4.11 mM) led to superior bone regeneration, while Mg(2+)-free and strong Mg(2+) content (~16.44 mM) discouraged cell adhesion, proliferation and osteogenic differentiation, thereby bone formation was rarely found. When magnesium ions diffused into free Mg zone from concentrated zone in late time point, new bone formation on free Mg zone became significant through intramembranous ossification. This study successfully demonstrates that magnesium cationic microenvironment serves as an effective biochemical cue and is able to modulate the process of bony tissue regeneration. The knowledge of how a Mg(2+) cationic microenvironment intertwines with cells and subsequent bone formation gained from this study may provide a new insight to develop the next generation of tissue-repairing biomaterials.
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spelling pubmed-74927742020-09-28 Stepwise 3D-spatio-temporal magnesium cationic niche: Nanocomposite scaffold mediated microenvironment for modulating intramembranous ossification Shen, Jie Chen, Bo Zhai, Xinyun Qiao, Wei Wu, Shuilin Liu, Xuanyong Zhao, Ying Ruan, Changshun Pan, Haobo Chu, Paul K. Cheung, Kenneth M.C. Yeung, Kelvin W.K. Bioact Mater Article The fate of cells and subsequent bone regeneration is highly correlated with temporospatial coordination of chemical, biological, or physical cues within a local tissue microenvironment. Deeper understanding of how mammalian cells react to local tissue microenvironment is paramount important when designing next generation of biomaterials for tissue engineering. This study aims to investigate that the regulation of magnesium cationic (Mg(2+)) tissue microenvironment is able to convince early-stage bone regeneration and its mechanism undergoes intramembranous ossification. It was discovered that moderate Mg(2+) content niche (~4.11 mM) led to superior bone regeneration, while Mg(2+)-free and strong Mg(2+) content (~16.44 mM) discouraged cell adhesion, proliferation and osteogenic differentiation, thereby bone formation was rarely found. When magnesium ions diffused into free Mg zone from concentrated zone in late time point, new bone formation on free Mg zone became significant through intramembranous ossification. This study successfully demonstrates that magnesium cationic microenvironment serves as an effective biochemical cue and is able to modulate the process of bony tissue regeneration. The knowledge of how a Mg(2+) cationic microenvironment intertwines with cells and subsequent bone formation gained from this study may provide a new insight to develop the next generation of tissue-repairing biomaterials. KeAi Publishing 2020-09-10 /pmc/articles/PMC7492774/ /pubmed/32995676 http://dx.doi.org/10.1016/j.bioactmat.2020.08.025 Text en © 2020 [The Author/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
Shen, Jie
Chen, Bo
Zhai, Xinyun
Qiao, Wei
Wu, Shuilin
Liu, Xuanyong
Zhao, Ying
Ruan, Changshun
Pan, Haobo
Chu, Paul K.
Cheung, Kenneth M.C.
Yeung, Kelvin W.K.
Stepwise 3D-spatio-temporal magnesium cationic niche: Nanocomposite scaffold mediated microenvironment for modulating intramembranous ossification
title Stepwise 3D-spatio-temporal magnesium cationic niche: Nanocomposite scaffold mediated microenvironment for modulating intramembranous ossification
title_full Stepwise 3D-spatio-temporal magnesium cationic niche: Nanocomposite scaffold mediated microenvironment for modulating intramembranous ossification
title_fullStr Stepwise 3D-spatio-temporal magnesium cationic niche: Nanocomposite scaffold mediated microenvironment for modulating intramembranous ossification
title_full_unstemmed Stepwise 3D-spatio-temporal magnesium cationic niche: Nanocomposite scaffold mediated microenvironment for modulating intramembranous ossification
title_short Stepwise 3D-spatio-temporal magnesium cationic niche: Nanocomposite scaffold mediated microenvironment for modulating intramembranous ossification
title_sort stepwise 3d-spatio-temporal magnesium cationic niche: nanocomposite scaffold mediated microenvironment for modulating intramembranous ossification
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7492774/
https://www.ncbi.nlm.nih.gov/pubmed/32995676
http://dx.doi.org/10.1016/j.bioactmat.2020.08.025
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