Targeted Repair of Spinal Cord Injury Based on miRNA‐124‐3p–Loaded Mesoporous Silica Camouflaged by Stem Cell Membrane Modified with Rabies Virus Glycoprotein

狂犬病病毒 脊髓损伤 介孔二氧化硅 轴突 干细胞 间充质干细胞 脊髓 化学 介孔材料 医学 细胞生物学 免疫学 生物 病毒 神经科学 生物化学 催化作用
作者
Xiangchuang Fan,Lusen Shi,Zimeng Yang,Yiwei Li,Chi Zhang,Baoshuai Bai,Lü Chen,Elzat Elham‐Yilizati Yilihamu,Zhangyang Qi,Wenxiang Li,Peng Xiao,Mingshan Liu,Jichuan Qiu,Fan Yang,Ning Ran,Yifan Shang,Jiaxing Liu,T. Zhang,Xiaohong Kong,Hong Liu
出处
期刊:Advanced Science [Wiley]
卷期号:11 (21): e2309305-e2309305 被引量:31
标识
DOI:10.1002/advs.202309305
摘要

Spinal cord injury (SCI) has no effective treatment modalities. It faces a significant global therapeutical challenge, given its features of poor axon regeneration, progressive local inflammation, and inefficient systemic drug delivery due to the blood-spinal cord barrier (BSCB). To address these challenges, a new nano complex that achieves targeted drug delivery to the damaged spinal cord is proposed, which contains a mesoporous silica nanoparticle core loaded with microRNA and a cloaking layer of human umbilical cord mesenchymal stem cell membrane modified with rabies virus glycoprotein (RVG). The nano complex more readily crosses the damaged BSCB with its exosome-resembling properties, including appropriate size and a low-immunogenic cell membrane disguise and accumulates in the injury center because of RVG, where it releases abundant microRNAs to elicit axon sprouting and rehabilitate the inflammatory microenvironment. Culturing with nano complexes promotes axonal growth in neurons and M2 polarization in microglia. Furthermore, it showed that SCI mice treated with this nano complex by tail vein injection display significant improvement in axon regrowth, microenvironment regulation, and functional restoration. The efficacy and biocompatibility of the targeted delivery of microRNA by nano complexes demonstrate their immense potential as a noninvasive treatment for SCI.
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