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A click chemistry-mediated all-peptide cell printing hydrogel platform for diabetic wound healing

High glucose-induced vascular endothelial injury is a major pathological factor involved in non-healing diabetic wounds. To interrupt this pathological process, we design an all-peptide printable hydrogel platform based on highly efficient and precise one-step click chemistry of thiolated γ-polyglut...

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Autores principales: Huang, Jinjian, Yang, Rong, Jiao, Jiao, Li, Ze, Wang, Penghui, Liu, Ye, Li, Sicheng, Chen, Canwen, Li, Zongan, Qu, Guiwen, Chen, Kang, Wu, Xiuwen, Chi, Bo, Ren, Jianan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10687272/
https://www.ncbi.nlm.nih.gov/pubmed/38030636
http://dx.doi.org/10.1038/s41467-023-43364-2
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author Huang, Jinjian
Yang, Rong
Jiao, Jiao
Li, Ze
Wang, Penghui
Liu, Ye
Li, Sicheng
Chen, Canwen
Li, Zongan
Qu, Guiwen
Chen, Kang
Wu, Xiuwen
Chi, Bo
Ren, Jianan
author_facet Huang, Jinjian
Yang, Rong
Jiao, Jiao
Li, Ze
Wang, Penghui
Liu, Ye
Li, Sicheng
Chen, Canwen
Li, Zongan
Qu, Guiwen
Chen, Kang
Wu, Xiuwen
Chi, Bo
Ren, Jianan
author_sort Huang, Jinjian
collection PubMed
description High glucose-induced vascular endothelial injury is a major pathological factor involved in non-healing diabetic wounds. To interrupt this pathological process, we design an all-peptide printable hydrogel platform based on highly efficient and precise one-step click chemistry of thiolated γ-polyglutamic acid, glycidyl methacrylate-conjugated γ-polyglutamic acid, and thiolated arginine-glycine-aspartate sequences. Vascular endothelial growth factor 165-overexpressed human umbilical vein endothelial cells are printed using this platform, hence fabricating a living material with high cell viability and precise cell spatial distribution control. This cell-laden hydrogel platform accelerates the diabetic wound healing of rats based on the unabated vascular endothelial growth factor 165 release, which promotes angiogenesis and alleviates damages on vascular endothelial mitochondria, thereby reducing tissue hypoxia, downregulating inflammation, and facilitating extracellular matrix remodeling. Together, this study offers a promising strategy for fabricating tissue-friendly, high-efficient, and accurate 3D printed all-peptide hydrogel platform for cell delivery and self-renewable growth factor therapy.
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spelling pubmed-106872722023-11-30 A click chemistry-mediated all-peptide cell printing hydrogel platform for diabetic wound healing Huang, Jinjian Yang, Rong Jiao, Jiao Li, Ze Wang, Penghui Liu, Ye Li, Sicheng Chen, Canwen Li, Zongan Qu, Guiwen Chen, Kang Wu, Xiuwen Chi, Bo Ren, Jianan Nat Commun Article High glucose-induced vascular endothelial injury is a major pathological factor involved in non-healing diabetic wounds. To interrupt this pathological process, we design an all-peptide printable hydrogel platform based on highly efficient and precise one-step click chemistry of thiolated γ-polyglutamic acid, glycidyl methacrylate-conjugated γ-polyglutamic acid, and thiolated arginine-glycine-aspartate sequences. Vascular endothelial growth factor 165-overexpressed human umbilical vein endothelial cells are printed using this platform, hence fabricating a living material with high cell viability and precise cell spatial distribution control. This cell-laden hydrogel platform accelerates the diabetic wound healing of rats based on the unabated vascular endothelial growth factor 165 release, which promotes angiogenesis and alleviates damages on vascular endothelial mitochondria, thereby reducing tissue hypoxia, downregulating inflammation, and facilitating extracellular matrix remodeling. Together, this study offers a promising strategy for fabricating tissue-friendly, high-efficient, and accurate 3D printed all-peptide hydrogel platform for cell delivery and self-renewable growth factor therapy. Nature Publishing Group UK 2023-11-29 /pmc/articles/PMC10687272/ /pubmed/38030636 http://dx.doi.org/10.1038/s41467-023-43364-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Huang, Jinjian
Yang, Rong
Jiao, Jiao
Li, Ze
Wang, Penghui
Liu, Ye
Li, Sicheng
Chen, Canwen
Li, Zongan
Qu, Guiwen
Chen, Kang
Wu, Xiuwen
Chi, Bo
Ren, Jianan
A click chemistry-mediated all-peptide cell printing hydrogel platform for diabetic wound healing
title A click chemistry-mediated all-peptide cell printing hydrogel platform for diabetic wound healing
title_full A click chemistry-mediated all-peptide cell printing hydrogel platform for diabetic wound healing
title_fullStr A click chemistry-mediated all-peptide cell printing hydrogel platform for diabetic wound healing
title_full_unstemmed A click chemistry-mediated all-peptide cell printing hydrogel platform for diabetic wound healing
title_short A click chemistry-mediated all-peptide cell printing hydrogel platform for diabetic wound healing
title_sort click chemistry-mediated all-peptide cell printing hydrogel platform for diabetic wound healing
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10687272/
https://www.ncbi.nlm.nih.gov/pubmed/38030636
http://dx.doi.org/10.1038/s41467-023-43364-2
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