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Size-dependent gold nanoparticles induce macrophage M2 polarization and promote intracellular clearance of Staphylococcus aureus to alleviate tissue infection

Tissue infection typically results from blood transmission or the direct inoculation of bacteria following trauma. The pathogen-induced destruction of tissue prevents antibiotics from penetrating the infected site, and severe inflammation further impairs the efficacy of conventional treatment. The c...

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Autores principales: Peilin, Wang, Ying, Peng, Renyuan, Wang, Zhuoxuan, Li, Zhenwu, Yang, Mai, Zhao, Jianguo, Song, Hao, Zhang, Gang, Yin, Lin, Lin, Haodong, Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10338365/
https://www.ncbi.nlm.nih.gov/pubmed/37455821
http://dx.doi.org/10.1016/j.mtbio.2023.100700
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author Peilin, Wang
Ying, Peng
Renyuan, Wang
Zhuoxuan, Li
Zhenwu, Yang
Mai, Zhao
Jianguo, Song
Hao, Zhang
Gang, Yin
Lin, Lin
Haodong, Lin
author_facet Peilin, Wang
Ying, Peng
Renyuan, Wang
Zhuoxuan, Li
Zhenwu, Yang
Mai, Zhao
Jianguo, Song
Hao, Zhang
Gang, Yin
Lin, Lin
Haodong, Lin
author_sort Peilin, Wang
collection PubMed
description Tissue infection typically results from blood transmission or the direct inoculation of bacteria following trauma. The pathogen-induced destruction of tissue prevents antibiotics from penetrating the infected site, and severe inflammation further impairs the efficacy of conventional treatment. The current study describes the size-dependent induction of macrophage polarization using gold nanoparticles. Gold nanoparticles with a diameter of 50 ​nm (Au50) can induce M2 polarization in macrophages by inhibiting the NF-κB signaling pathway and stimulate an inflammatory response in the environment by inhibiting the MAPK signaling pathway LPS. Furthermore, the induced polarization and anti-inflammatory effects of the Au50 nanoparticles promoted the osteogenic differentiation of BMSCs in vitro. In addition, the overexpression of TREM2 in macrophage induced by Au50 nanoparticles was found to promote macrophage phagocytosis of Staphylococcus aureus, enhance the fusion of autophagosomes and lysosomes, accelerate the intracellular degradation of S. aureus, in addition to achieving an effective local treatment of osteomyelitis and infectious skin defects in conjunction with inflammatory regulation and accelerating bone regeneration. The findings, therefore, demonstrate that Au50 nanoparticles can be utilized as a promising nanomaterial for in vivo treatment of infections.
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spelling pubmed-103383652023-07-14 Size-dependent gold nanoparticles induce macrophage M2 polarization and promote intracellular clearance of Staphylococcus aureus to alleviate tissue infection Peilin, Wang Ying, Peng Renyuan, Wang Zhuoxuan, Li Zhenwu, Yang Mai, Zhao Jianguo, Song Hao, Zhang Gang, Yin Lin, Lin Haodong, Lin Mater Today Bio Full Length Article Tissue infection typically results from blood transmission or the direct inoculation of bacteria following trauma. The pathogen-induced destruction of tissue prevents antibiotics from penetrating the infected site, and severe inflammation further impairs the efficacy of conventional treatment. The current study describes the size-dependent induction of macrophage polarization using gold nanoparticles. Gold nanoparticles with a diameter of 50 ​nm (Au50) can induce M2 polarization in macrophages by inhibiting the NF-κB signaling pathway and stimulate an inflammatory response in the environment by inhibiting the MAPK signaling pathway LPS. Furthermore, the induced polarization and anti-inflammatory effects of the Au50 nanoparticles promoted the osteogenic differentiation of BMSCs in vitro. In addition, the overexpression of TREM2 in macrophage induced by Au50 nanoparticles was found to promote macrophage phagocytosis of Staphylococcus aureus, enhance the fusion of autophagosomes and lysosomes, accelerate the intracellular degradation of S. aureus, in addition to achieving an effective local treatment of osteomyelitis and infectious skin defects in conjunction with inflammatory regulation and accelerating bone regeneration. The findings, therefore, demonstrate that Au50 nanoparticles can be utilized as a promising nanomaterial for in vivo treatment of infections. Elsevier 2023-06-20 /pmc/articles/PMC10338365/ /pubmed/37455821 http://dx.doi.org/10.1016/j.mtbio.2023.100700 Text en © 2023 The Author(s) 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 Full Length Article
Peilin, Wang
Ying, Peng
Renyuan, Wang
Zhuoxuan, Li
Zhenwu, Yang
Mai, Zhao
Jianguo, Song
Hao, Zhang
Gang, Yin
Lin, Lin
Haodong, Lin
Size-dependent gold nanoparticles induce macrophage M2 polarization and promote intracellular clearance of Staphylococcus aureus to alleviate tissue infection
title Size-dependent gold nanoparticles induce macrophage M2 polarization and promote intracellular clearance of Staphylococcus aureus to alleviate tissue infection
title_full Size-dependent gold nanoparticles induce macrophage M2 polarization and promote intracellular clearance of Staphylococcus aureus to alleviate tissue infection
title_fullStr Size-dependent gold nanoparticles induce macrophage M2 polarization and promote intracellular clearance of Staphylococcus aureus to alleviate tissue infection
title_full_unstemmed Size-dependent gold nanoparticles induce macrophage M2 polarization and promote intracellular clearance of Staphylococcus aureus to alleviate tissue infection
title_short Size-dependent gold nanoparticles induce macrophage M2 polarization and promote intracellular clearance of Staphylococcus aureus to alleviate tissue infection
title_sort size-dependent gold nanoparticles induce macrophage m2 polarization and promote intracellular clearance of staphylococcus aureus to alleviate tissue infection
topic Full Length Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10338365/
https://www.ncbi.nlm.nih.gov/pubmed/37455821
http://dx.doi.org/10.1016/j.mtbio.2023.100700
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