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ECM-mimetic immunomodulatory hydrogel for methicillin-resistant Staphylococcus aureus–infected chronic skin wound healing

The treatment of difficult-to-heal wounds remains a substantial clinical challenge due to deteriorative tissue microenvironment including the loss of extracellular matrix (ECM), excessive inflammation, impaired angiogenesis, and bacterial infection. Inspired by the chemical components, fibrous struc...

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Autores principales: Liu, Wenshuai, Gao, Rui, Yang, Chunfang, Feng, Zujian, Ou-Yang, Wenbin, Pan, Xiangbin, Huang, Pingsheng, Zhang, Chuangnian, Kong, Deling, Wang, Weiwei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9269894/
https://www.ncbi.nlm.nih.gov/pubmed/35857459
http://dx.doi.org/10.1126/sciadv.abn7006
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author Liu, Wenshuai
Gao, Rui
Yang, Chunfang
Feng, Zujian
Ou-Yang, Wenbin
Pan, Xiangbin
Huang, Pingsheng
Zhang, Chuangnian
Kong, Deling
Wang, Weiwei
author_facet Liu, Wenshuai
Gao, Rui
Yang, Chunfang
Feng, Zujian
Ou-Yang, Wenbin
Pan, Xiangbin
Huang, Pingsheng
Zhang, Chuangnian
Kong, Deling
Wang, Weiwei
author_sort Liu, Wenshuai
collection PubMed
description The treatment of difficult-to-heal wounds remains a substantial clinical challenge due to deteriorative tissue microenvironment including the loss of extracellular matrix (ECM), excessive inflammation, impaired angiogenesis, and bacterial infection. Inspired by the chemical components, fibrous structure, and biological function of natural ECM, antibacterial and tissue environment–responsive glycopeptide hybrid hydrogel was developed for chronic wound healing. The hydrogel can facilitate the cell proliferation and macrophage polarization to M2 phenotype, and show potent antibacterial efficacy against both Gram-negative and Gram-positive bacteria. Significantly, the glycopeptide hydrogel accelerated the reconstruction of methicillin-resistant Staphylococcus aureus (MRSA)–infected full-thickness diabetic and scalding skin by orchestrating a pro-regenerative response indicated by abundant M2-type macrophages, attenuated inflammation, and promoted angiogenesis. Collectively, ECM-mimetic and immunomodulatory glycopeptide hydrogel is a promising multifunctional dressing to reshape the damaged tissue environment without additional drugs, exogenous cytokines, or cells, providing an effective strategy for the repair and regeneration of chronic cutaneous wounds.
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spelling pubmed-92698942022-07-20 ECM-mimetic immunomodulatory hydrogel for methicillin-resistant Staphylococcus aureus–infected chronic skin wound healing Liu, Wenshuai Gao, Rui Yang, Chunfang Feng, Zujian Ou-Yang, Wenbin Pan, Xiangbin Huang, Pingsheng Zhang, Chuangnian Kong, Deling Wang, Weiwei Sci Adv Biomedicine and Life Sciences The treatment of difficult-to-heal wounds remains a substantial clinical challenge due to deteriorative tissue microenvironment including the loss of extracellular matrix (ECM), excessive inflammation, impaired angiogenesis, and bacterial infection. Inspired by the chemical components, fibrous structure, and biological function of natural ECM, antibacterial and tissue environment–responsive glycopeptide hybrid hydrogel was developed for chronic wound healing. The hydrogel can facilitate the cell proliferation and macrophage polarization to M2 phenotype, and show potent antibacterial efficacy against both Gram-negative and Gram-positive bacteria. Significantly, the glycopeptide hydrogel accelerated the reconstruction of methicillin-resistant Staphylococcus aureus (MRSA)–infected full-thickness diabetic and scalding skin by orchestrating a pro-regenerative response indicated by abundant M2-type macrophages, attenuated inflammation, and promoted angiogenesis. Collectively, ECM-mimetic and immunomodulatory glycopeptide hydrogel is a promising multifunctional dressing to reshape the damaged tissue environment without additional drugs, exogenous cytokines, or cells, providing an effective strategy for the repair and regeneration of chronic cutaneous wounds. American Association for the Advancement of Science 2022-07-08 /pmc/articles/PMC9269894/ /pubmed/35857459 http://dx.doi.org/10.1126/sciadv.abn7006 Text en Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Biomedicine and Life Sciences
Liu, Wenshuai
Gao, Rui
Yang, Chunfang
Feng, Zujian
Ou-Yang, Wenbin
Pan, Xiangbin
Huang, Pingsheng
Zhang, Chuangnian
Kong, Deling
Wang, Weiwei
ECM-mimetic immunomodulatory hydrogel for methicillin-resistant Staphylococcus aureus–infected chronic skin wound healing
title ECM-mimetic immunomodulatory hydrogel for methicillin-resistant Staphylococcus aureus–infected chronic skin wound healing
title_full ECM-mimetic immunomodulatory hydrogel for methicillin-resistant Staphylococcus aureus–infected chronic skin wound healing
title_fullStr ECM-mimetic immunomodulatory hydrogel for methicillin-resistant Staphylococcus aureus–infected chronic skin wound healing
title_full_unstemmed ECM-mimetic immunomodulatory hydrogel for methicillin-resistant Staphylococcus aureus–infected chronic skin wound healing
title_short ECM-mimetic immunomodulatory hydrogel for methicillin-resistant Staphylococcus aureus–infected chronic skin wound healing
title_sort ecm-mimetic immunomodulatory hydrogel for methicillin-resistant staphylococcus aureus–infected chronic skin wound healing
topic Biomedicine and Life Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9269894/
https://www.ncbi.nlm.nih.gov/pubmed/35857459
http://dx.doi.org/10.1126/sciadv.abn7006
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