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Titanium dioxide nanotubes promote M2 polarization by inhibiting macrophage glycolysis and ultimately accelerate endothelialization

Titanium has been widely used in prosthetic valves, but they are associated with serious defects in titanium‐based prosthetic valves, such as thrombosis, calcification, and decay. Therefore, it is very important to biofunctionalize titanium‐based valves to reduce inflammation and accelerate endothel...

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Autores principales: Yu, Wen P., Ding, Jing L., Liu, Xin L., Zhu, Guo D., Lin, Feng, Xu, Jian J., Wang, Ziyao, Zhou, Jian L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8342206/
https://www.ncbi.nlm.nih.gov/pubmed/33835721
http://dx.doi.org/10.1002/iid3.429
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author Yu, Wen P.
Ding, Jing L.
Liu, Xin L.
Zhu, Guo D.
Lin, Feng
Xu, Jian J.
Wang, Ziyao
Zhou, Jian L.
author_facet Yu, Wen P.
Ding, Jing L.
Liu, Xin L.
Zhu, Guo D.
Lin, Feng
Xu, Jian J.
Wang, Ziyao
Zhou, Jian L.
author_sort Yu, Wen P.
collection PubMed
description Titanium has been widely used in prosthetic valves, but they are associated with serious defects in titanium‐based prosthetic valves, such as thrombosis, calcification, and decay. Therefore, it is very important to biofunctionalize titanium‐based valves to reduce inflammation and accelerate endothelialization of stents and antithrombosis. The titanium dioxide nanotubes were prepared from pure titanium (Ti) by anodic oxidation method in this study. The effects of titanium dioxide nanotubes on the metabolism of macrophages and the inflammatory reaction as implants were studied in vitro. The polarization state of macrophages and the ability to accelerate endothelialization were analyzed. The results demonstrated that titanium nanotubes promote M2 polarization of macrophages by inhibiting glycolysis and activating the Adenosine monophosphate‐activated protein kinase (AMPK) signaling pathway. In general, biofunctionalization titanium with nanotube could inhibit macrophage glycolysis, reduce inflammatory factor release and promote M2 polarization by activating the AMPK signaling pathway. And endothelialization was accelerated in vitro. Our result demonstrated that titanium nanotube could act as a potential approach to biofunctionlize titanium‐based prosthetic valves for endothelialization.
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spelling pubmed-83422062021-08-11 Titanium dioxide nanotubes promote M2 polarization by inhibiting macrophage glycolysis and ultimately accelerate endothelialization Yu, Wen P. Ding, Jing L. Liu, Xin L. Zhu, Guo D. Lin, Feng Xu, Jian J. Wang, Ziyao Zhou, Jian L. Immun Inflamm Dis Original Articles Titanium has been widely used in prosthetic valves, but they are associated with serious defects in titanium‐based prosthetic valves, such as thrombosis, calcification, and decay. Therefore, it is very important to biofunctionalize titanium‐based valves to reduce inflammation and accelerate endothelialization of stents and antithrombosis. The titanium dioxide nanotubes were prepared from pure titanium (Ti) by anodic oxidation method in this study. The effects of titanium dioxide nanotubes on the metabolism of macrophages and the inflammatory reaction as implants were studied in vitro. The polarization state of macrophages and the ability to accelerate endothelialization were analyzed. The results demonstrated that titanium nanotubes promote M2 polarization of macrophages by inhibiting glycolysis and activating the Adenosine monophosphate‐activated protein kinase (AMPK) signaling pathway. In general, biofunctionalization titanium with nanotube could inhibit macrophage glycolysis, reduce inflammatory factor release and promote M2 polarization by activating the AMPK signaling pathway. And endothelialization was accelerated in vitro. Our result demonstrated that titanium nanotube could act as a potential approach to biofunctionlize titanium‐based prosthetic valves for endothelialization. John Wiley and Sons Inc. 2021-04-09 /pmc/articles/PMC8342206/ /pubmed/33835721 http://dx.doi.org/10.1002/iid3.429 Text en © 2021 The Authors. Immunity, Inflammation and Disease published by John Wiley & Sons Ltd https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Yu, Wen P.
Ding, Jing L.
Liu, Xin L.
Zhu, Guo D.
Lin, Feng
Xu, Jian J.
Wang, Ziyao
Zhou, Jian L.
Titanium dioxide nanotubes promote M2 polarization by inhibiting macrophage glycolysis and ultimately accelerate endothelialization
title Titanium dioxide nanotubes promote M2 polarization by inhibiting macrophage glycolysis and ultimately accelerate endothelialization
title_full Titanium dioxide nanotubes promote M2 polarization by inhibiting macrophage glycolysis and ultimately accelerate endothelialization
title_fullStr Titanium dioxide nanotubes promote M2 polarization by inhibiting macrophage glycolysis and ultimately accelerate endothelialization
title_full_unstemmed Titanium dioxide nanotubes promote M2 polarization by inhibiting macrophage glycolysis and ultimately accelerate endothelialization
title_short Titanium dioxide nanotubes promote M2 polarization by inhibiting macrophage glycolysis and ultimately accelerate endothelialization
title_sort titanium dioxide nanotubes promote m2 polarization by inhibiting macrophage glycolysis and ultimately accelerate endothelialization
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8342206/
https://www.ncbi.nlm.nih.gov/pubmed/33835721
http://dx.doi.org/10.1002/iid3.429
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