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241022s2024 xx |||||o 00| ||eng c |
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|a 10.1002/adma.202410962
|2 doi
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|a pubmed24n1629.xml
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|a (DE-627)NLM379229420
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|a (NLM)39436107
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|a DE-627
|b ger
|c DE-627
|e rakwb
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|a eng
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|a Lin, Peihua
|e verfasserin
|4 aut
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|a A Single-Cell RNA Sequencing Guided Multienzymatic Hydrogel Design for Self-Regenerative Repair in Diabetic Mandibular Defects
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|c 2024
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|a Text
|b txt
|2 rdacontent
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|a ƒaComputermedien
|b c
|2 rdamedia
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|a ƒa Online-Ressource
|b cr
|2 rdacarrier
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|a Date Completed 12.12.2024
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|a Date Revised 12.12.2024
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|a published: Print-Electronic
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|a Citation Status MEDLINE
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|a © 2024 Wiley‐VCH GmbH.
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|a Conventional bone tissue engineering materials struggle to reinstate physiological bone remodeling in a diabetic context, primarily due to the compromised repolarization of proinflammatory macrophages to anti-inflammatory macrophages. Here, leveraging single-cell RNA sequencing (scRNA-seq) technology, the pivotal role of nitric oxide (NO) and reactive oxygen species (ROS) is unveiled in impeding macrophage repolarization during physiological bone remodeling amidst diabetes. Guided by scRNA-seq analysis, we engineer a multienzymatic bone tissue engineering hydrogel scaffold (MEBTHS) composed is engineered of methylpropenylated gelatin hydrogel integrated with ruthenium nanozymes, possessing both Ru0 and Ru4+ components. This design facilitates efficient NO elimination via Ru0 while simultaneously exhibiting ROS scavenging properties through Ru4+. Consequently, MEBTHS orchestrates macrophage reprogramming by neutralizing ROS and reversing NO-mediated mitochondrial metabolism, thereby rejuvenating bone marrow-derived mesenchymal stem cells and endothelial cells within diabetic mandibular defects, producing newly formed bone with quality comparable to that of normal bone. The scRNA-seq guided multienzymatic hydrogel design fosters the restoration of self-regenerative repair, marking a significant advancement in bone tissue engineering
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|a Journal Article
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|a Ru nanozyme
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|a diabetic mandibular defects
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|a multienzymatic hydrogel
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|a self‐regenerative repair
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|a single‐cell RNA sequencing
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|a Hydrogels
|2 NLM
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|a Nitric Oxide
|2 NLM
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|a 31C4KY9ESH
|2 NLM
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|a Reactive Oxygen Species
|2 NLM
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|a Qian, Zhouyang
|e verfasserin
|4 aut
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|a Liu, Shanbiao
|e verfasserin
|4 aut
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|a Ye, Xin
|e verfasserin
|4 aut
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|a Xue, Pengpeng
|e verfasserin
|4 aut
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|a Shao, Yangjie
|e verfasserin
|4 aut
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|a Zhao, Jing
|e verfasserin
|4 aut
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|a Guan, Yunan
|e verfasserin
|4 aut
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|a Liu, Zhichao
|e verfasserin
|4 aut
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|a Chen, Yuhua
|e verfasserin
|4 aut
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|a Wang, Qiyue
|e verfasserin
|4 aut
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|a Yi, Zhigao
|e verfasserin
|4 aut
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|a Zhu, Mingjian
|e verfasserin
|4 aut
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|a Yu, Mengfei
|e verfasserin
|4 aut
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|a Ling, Daishun
|e verfasserin
|4 aut
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|a Li, Fangyuan
|e verfasserin
|4 aut
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|i Enthalten in
|t Advanced materials (Deerfield Beach, Fla.)
|d 1998
|g 36(2024), 50 vom: 01. Dez., Seite e2410962
|w (DE-627)NLM098206397
|x 1521-4095
|7 nnns
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|g volume:36
|g year:2024
|g number:50
|g day:01
|g month:12
|g pages:e2410962
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|u http://dx.doi.org/10.1002/adma.202410962
|3 Volltext
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|d 36
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