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仿生“特洛伊木马”纤维调节先天免疫级联反应以促进神经再生。

Biomimetic "Trojan Horse" Fibers Modulate Innate Immunity Cascades for Nerve Regeneration.

作者信息

Wu Jie, Tang Jincheng, Zhang Lichen, Wang Wei, Li Ziang, Zhou Liang, Jiang Xinzhao, Huang Yiyang, Guo Qiangqiang, Wang Wenbo, Ding Zhouye, Cai Feng, Xi Kun, Gu Yong, Chen Liang

机构信息

Department of Orthopedics, The First Affiliated Hospital of Soochow University, 899 Pinghai Road, Suzhou 215006, Jiangsu, China.

出版信息

ACS Nano. 2025 Jan 14;19(1):781-802. doi: 10.1021/acsnano.4c12036. Epub 2024 Dec 21.

Abstract

Neutrophil membrane vesicles (NMVs) have been successfully applied to control the inflammatory cascade after spinal cord injury (SCI) by acting as an inflammatory factor decoy to front-load the overall inflammation regulatory window; however, the mechanisms by which NMVs regulate macrophage phenotypic shifts as well as their outcomes have rarely been reported. In this study, we demonstrated the "efferocytosis-like" effect of NMVs endocytosed by macrophages, supplementing the TCA cycle intermediate metabolite α-KG by promoting glutamine metabolism, which in turn facilitates oxidative phosphorylation and inhibits the NF-κB signaling pathway to reprogram inflammatory macrophages to the pro-regenerative phenotype. Based on these findings, a "Trojan horse" composite fiber scaffold was constructed; this comprised a carboxylated poly-l-lactic acid shell encapsulated with NMVs and a core loaded with brain-derived neurotrophic factor to spatiotemporally modulate the inflammatory microenvironment by 39.23% and sustainably promote nerve regeneration by 85.67%. In vivo experiments further confirmed the effect of NMV-coated fiber scaffolds on the regulation of early innate immune inflammation and the continuous promotion of nerve regeneration. This study not only further unravels the mechanism of neutrophil membrane-macrophage interactions but also provides a strategy for coordinating inflammatory reprogramming and nerve regeneration following SCI.

摘要

中性粒细胞膜囊泡(NMVs)已成功应用于脊髓损伤(SCI)后控制炎症级联反应,它作为炎症因子诱饵提前开启整个炎症调节窗口;然而,NMVs调节巨噬细胞表型转变的机制及其结果鲜有报道。在本研究中,我们展示了巨噬细胞内吞NMVs的“类吞噬作用”效应,通过促进谷氨酰胺代谢补充三羧酸循环中间代谢物α-酮戊二酸,进而促进氧化磷酸化并抑制NF-κB信号通路,将炎症巨噬细胞重编程为促再生表型。基于这些发现,构建了一种“特洛伊木马”复合纤维支架;它由包裹有NMVs的羧基化聚左旋乳酸外壳和负载脑源性神经营养因子的核心组成,可时空调节炎症微环境达39.23%,并可持续促进神经再生达85.67%。体内实验进一步证实了NMVs包被的纤维支架对早期先天性免疫炎症调节和神经再生持续促进的作用。本研究不仅进一步揭示了中性粒细胞膜与巨噬细胞相互作用的机制,还为脊髓损伤后协调炎症重编程和神经再生提供了一种策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68a3/11752508/c4171fc02a94/nn4c12036_0011.jpg

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