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用细胞外囊泡功能化的脱细胞组织基质水凝胶可促进巨噬细胞重编程和神经干细胞分化,用于脊髓损伤修复。

Decellularized tissue matrices hydrogels functionalized with extracellular vesicles promote macrophage reprogramming and neural stem cell differentiation for spinal cord injury repair.

作者信息

Deng Ming, Xie Ping, Xue Hongyang, Chen Qing, Zhou Yan, Ming Jianghua, Ma Yonggang, Liu Junqi, Huang Hui

机构信息

Department of Orthopedics, Renmin Hospital of Wuhan University, Wuhan, 430060, China.

Department of Chinese Traditional Medicine, Tongren Hospital of Wuhan University (Wuhan Third Hospital), Wuhan, 430060, China.

出版信息

J Nanobiotechnology. 2025 Feb 25;23(1):139. doi: 10.1186/s12951-025-03152-0.

Abstract

This study investigates the application of decellularized tissue matrices (DSCM) hydrogels functionalized with extracellular vesicles (EVs) derived from mesenchymal stromal cells (MSCs) for spinal cord injury (SCI) treatment. The primary focus is on how these composites influence macrophage reprogramming and neural stem cell (NSC) differentiation by modulating Slamf9 expression. MSC-derived EVs were successfully isolated, and DSCM hydrogels were prepared from porcine spinal cords. The composite material, EVs derived from MSCs (DSCM@EVs), was constructed and applied to a mouse SCI model, showing significant enhancement in NSC differentiation and axonal growth, thereby alleviating SCI. Bioinformatics and in vitro cell experiments revealed that DSCM@EVs promote the reprogramming of M1 macrophages to the M2 phenotype, reducing inflammatory responses and facilitating NSC differentiation. RNA-seq analysis identified Slamf9 as a key regulatory gene, with its suppression linked to the observed therapeutic effects. This novel approach demonstrates the potential of DSCM@EVs in SCI repair by modulating the inflammatory environment and promoting neural regeneration, offering a promising strategy for treating SCI and potentially other inflammatory neurological disorders.

摘要

本研究探讨了用间充质基质细胞(MSC)来源的细胞外囊泡(EV)功能化的脱细胞组织基质(DSCM)水凝胶在脊髓损伤(SCI)治疗中的应用。主要关注这些复合材料如何通过调节Slamf9表达来影响巨噬细胞重编程和神经干细胞(NSC)分化。成功分离出MSC来源的EV,并从猪脊髓制备了DSCM水凝胶。构建了复合材料——MSC来源的EV(DSCM@EV),并将其应用于小鼠SCI模型,结果显示NSC分化和轴突生长显著增强,从而减轻了SCI。生物信息学和体外细胞实验表明,DSCM@EV促进M1巨噬细胞重编程为M2表型,减少炎症反应并促进NSC分化。RNA测序分析确定Slamf9为关键调控基因,其抑制与观察到的治疗效果相关。这种新方法证明了DSCM@EV通过调节炎症环境和促进神经再生在SCI修复中的潜力,为治疗SCI以及潜在的其他炎症性神经系统疾病提供了一种有前景的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a44/11853540/d6018f1fcdef/12951_2025_3152_Fig1_HTML.jpg

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