Suppr超能文献

一种用于主动靶向中性粒细胞胞外陷阱和脊髓损伤治疗的仿生抗神经炎症纳米平台。

A biomimic anti-neuroinflammatory nanoplatform for active neutrophil extracellular traps targeting and spinal cord injury therapy.

作者信息

Tang Chunming, Jin Yaoyao, Wu Min, Jia Feng, Lu Xiaowei, Li Jinyu, Wu Jie, Zhu Senlin, Wang Zhiji, An Di, Xiong Wu, Zhang Yongjie, Xu Huae, Chen Xufeng

机构信息

Department of Pharmaceutics, School of Pharmacy, Nanjing Medical University, Nanjing, 211166, China.

Department of Emergency, The Affiliated Huai'an Hospital of Xuzhou Medical University and The Second People's Hospital of Huai'an, Huai'an, 223022, China.

出版信息

Mater Today Bio. 2024 Aug 24;28:101218. doi: 10.1016/j.mtbio.2024.101218. eCollection 2024 Oct.

Abstract

Traumatic spinal cord injury (SCI) always leads to severe neurological deficits and permanent damage. Neuroinflammation is a vital process of SCI and have become a promising target for SCI treatment. However, the neuroinflammation-targeted therapy would hinder the functional recovery of spinal cord and lead to the treatment failure. Herein, a biomimic anti-neuroinflammatory nanoplatform (DHCNPs) was developed for active neutrophil extracellular traps (NETs) targeting and SCI treatment. The curcumin-loaded liposome with the anti-inflammatory property acted as the core of the DHCNPs. Platelet membrane and neutrophil membrane were fused to form the biomimic hybrid membrane of the DHCNPs for hijacking neutrophils and neutralizing the elevated neutrophil-related proinflammatory cytokines, respectively. DNAse I modification on the hybrid membrane could achieve NETs degradation, blood spinal cord barrier, and neuron repair. Further studies proved that the DHCNPs could reprogram the multifaceted neuroinflammation and reverse the SCI process via nuclear factor kappa-B (NF-κB) pathway. We believe that the current study provides a new perspective for neuroinflammation inhibition and may shed new light on the treatment of SCI.

摘要

创伤性脊髓损伤(SCI)总会导致严重的神经功能缺损和永久性损伤。神经炎症是SCI的一个重要过程,已成为SCI治疗的一个有前景的靶点。然而,以神经炎症为靶点的治疗会阻碍脊髓功能恢复并导致治疗失败。在此,我们开发了一种仿生抗神经炎症纳米平台(DHCNPs)用于靶向活性中性粒细胞胞外陷阱(NETs)及治疗SCI。具有抗炎特性的载姜黄素脂质体作为DHCNPs的核心。血小板膜和中性粒细胞膜融合形成DHCNPs的仿生杂化膜,分别用于劫持中性粒细胞和中和升高的中性粒细胞相关促炎细胞因子。杂化膜上的脱氧核糖核酸酶I修饰可实现NETs降解、血脊髓屏障修复及神经元修复。进一步研究证明,DHCNPs可通过核因子κB(NF-κB)途径对多方面的神经炎症进行重编程并逆转SCI进程。我们相信,当前的研究为神经炎症抑制提供了新的视角,可能为SCI的治疗带来新的启示。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验