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Shifting focus from bacteria to host neutrophil extracellular traps of biodegradable pure Zn to combat implant centered infection
The widespread use of orthopedic implants to support or replace bones is increasingly threatened by the risk of incurable bacterial infections, impenetrable microbial biofilms, and irreversible antibiotic resistance. In the past, the development of anti-infective biomaterials focused solely on direc...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
KeAi Publishing
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9483647/ https://www.ncbi.nlm.nih.gov/pubmed/36185738 http://dx.doi.org/10.1016/j.bioactmat.2022.09.004 |
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author | Peng, Feng Xie, Juning Liu, Haiming Zheng, Yufeng Qian, Xin Zhou, Ruixiang Zhong, Hua Zhang, Yu Li, Mei |
author_facet | Peng, Feng Xie, Juning Liu, Haiming Zheng, Yufeng Qian, Xin Zhou, Ruixiang Zhong, Hua Zhang, Yu Li, Mei |
author_sort | Peng, Feng |
collection | PubMed |
description | The widespread use of orthopedic implants to support or replace bones is increasingly threatened by the risk of incurable bacterial infections, impenetrable microbial biofilms, and irreversible antibiotic resistance. In the past, the development of anti-infective biomaterials focused solely on direct antibacterial properties while ignoring the host's immune response. Inspired by the clearance of infection by the innate neutrophil response and participation in anti-infectious immunity of Zn ions, we report an innovative neutrophil extracellular traps (NETs) strategy, induced by biodegradable pure Zn, which achieved therapeutic efficacy toward biomaterial-related infections. Our in vitro and in vivo data showed that pure Zn was favorable for NETs formation by promoting the release of DNA fibers and granule proteins in a reactive oxygen species (ROS)-dependent manner, thereby retraining and degrading bacteria with an efficiency of up to 99.5%. Transcriptome analysis revealed that cytoskeletal rearrangement and toll-like receptor (TLR) signaling pathway were also involved in Zn-induced NETs formation. Furthermore, the in vivo results of a Staphylococcus aureus (S. aureus)-infected rat model verified that pure Zn potentiated the bactericidal capability of neutrophils around implants, and promoted osseointegration in S. aureus-infected rat femurs. This antibacterial immunity concept lays a foundation for the development of other antibacterial biomaterials and holds great promise for treating orthopedic infections. |
format | Online Article Text |
id | pubmed-9483647 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | KeAi Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-94836472022-09-30 Shifting focus from bacteria to host neutrophil extracellular traps of biodegradable pure Zn to combat implant centered infection Peng, Feng Xie, Juning Liu, Haiming Zheng, Yufeng Qian, Xin Zhou, Ruixiang Zhong, Hua Zhang, Yu Li, Mei Bioact Mater Article The widespread use of orthopedic implants to support or replace bones is increasingly threatened by the risk of incurable bacterial infections, impenetrable microbial biofilms, and irreversible antibiotic resistance. In the past, the development of anti-infective biomaterials focused solely on direct antibacterial properties while ignoring the host's immune response. Inspired by the clearance of infection by the innate neutrophil response and participation in anti-infectious immunity of Zn ions, we report an innovative neutrophil extracellular traps (NETs) strategy, induced by biodegradable pure Zn, which achieved therapeutic efficacy toward biomaterial-related infections. Our in vitro and in vivo data showed that pure Zn was favorable for NETs formation by promoting the release of DNA fibers and granule proteins in a reactive oxygen species (ROS)-dependent manner, thereby retraining and degrading bacteria with an efficiency of up to 99.5%. Transcriptome analysis revealed that cytoskeletal rearrangement and toll-like receptor (TLR) signaling pathway were also involved in Zn-induced NETs formation. Furthermore, the in vivo results of a Staphylococcus aureus (S. aureus)-infected rat model verified that pure Zn potentiated the bactericidal capability of neutrophils around implants, and promoted osseointegration in S. aureus-infected rat femurs. This antibacterial immunity concept lays a foundation for the development of other antibacterial biomaterials and holds great promise for treating orthopedic infections. KeAi Publishing 2022-09-15 /pmc/articles/PMC9483647/ /pubmed/36185738 http://dx.doi.org/10.1016/j.bioactmat.2022.09.004 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 Peng, Feng Xie, Juning Liu, Haiming Zheng, Yufeng Qian, Xin Zhou, Ruixiang Zhong, Hua Zhang, Yu Li, Mei Shifting focus from bacteria to host neutrophil extracellular traps of biodegradable pure Zn to combat implant centered infection |
title | Shifting focus from bacteria to host neutrophil extracellular traps of biodegradable pure Zn to combat implant centered infection |
title_full | Shifting focus from bacteria to host neutrophil extracellular traps of biodegradable pure Zn to combat implant centered infection |
title_fullStr | Shifting focus from bacteria to host neutrophil extracellular traps of biodegradable pure Zn to combat implant centered infection |
title_full_unstemmed | Shifting focus from bacteria to host neutrophil extracellular traps of biodegradable pure Zn to combat implant centered infection |
title_short | Shifting focus from bacteria to host neutrophil extracellular traps of biodegradable pure Zn to combat implant centered infection |
title_sort | shifting focus from bacteria to host neutrophil extracellular traps of biodegradable pure zn to combat implant centered infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9483647/ https://www.ncbi.nlm.nih.gov/pubmed/36185738 http://dx.doi.org/10.1016/j.bioactmat.2022.09.004 |
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