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微环境自适应纳米药物通过抑制炎症级联反应和神经细胞凋亡促进脊髓修复。

Microenvironment Self-Adaptive Nanomedicine Promotes Spinal Cord Repair by Suppressing Inflammation Cascade and Neural Apoptosis.

作者信息

Qian Dingfei, Xu Jiaqi, Zhang Xuelian, Hu Fanqi, Cao Shiqi, Dong Yuan, Liu Xiaole, Yao Yawei, Yu Haichao, Lu Yichao, Ma Xiaotu, Cheng Keman, Zhao Xiao, Nie Guangjun, Zhang Xuesong

机构信息

Department of Orthopedics, Chinese PLA General Hospital, 28 Fuxing Road, Haidian District, Beijing, 100853, China.

Department of Orthopedics, The Fourth Medical Center, Chinese PLA General Hospital, 51 Fucheng Road, Haidian District, Beijing, 100048, China.

出版信息

Adv Mater. 2024 Dec;36(50):e2307624. doi: 10.1002/adma.202307624. Epub 2024 Oct 31.

Abstract

Despite various biomaterial-based strategies are tried in spinal cord injury (SCI), developing safe and effective microinvasive pharmacotherapy strategies is still an unmet clinical need. Stimuli-responsive nanomedicine has emerged as a promising non-invasion technology, which enhances drug delivery and promotes functional recovery following SCI. Considering the multiple progressive pathological events and the blood spinal cord barrier (BSCB) associating SCI, a microenvironment self-adaptive nanoparticle (custom-designed with rabies virus glycoprotein 29-RVG29 and hyaluronic acid-HA, RHNP) capable of consistently crossing the BSCB and selectively targeting inflammatory cells and neural cells based on different stages of SCI are developed. The data indicated that RHNP can effectively traverse the BSCB through RVG29, and adaptively modulate cellular internalization by selectively exposing either HA or RVG29 through diselenide bonds, depending on pathological reactive oxygen species (ROS) signals. Furthermore, curcumin is loaded into RHNP (RHNP-Cur) to improve motor function and coordination of hind-limbs in a traumatic SCI mouse model. This study finds that RHNP-Cur exhibited inhibitory effects on the inflammatory cascade originating from M1 microglia/macrophages and neurotoxic astrocytes, and protected neural cells from inflammation-induced apoptosis during nerve regeneration. Collectively, the work provides a microenvironment self-adaptive nanomedicine which enables efficient microinvasive treatment of SCI.

摘要

尽管在脊髓损伤(SCI)中尝试了各种基于生物材料的策略,但开发安全有效的微创药物治疗策略仍然是尚未满足的临床需求。刺激响应性纳米药物已成为一种有前途的非侵入性技术,可增强药物递送并促进SCI后的功能恢复。考虑到与SCI相关的多种进行性病理事件和血脊髓屏障(BSCB),开发了一种能够持续穿过BSCB并根据SCI的不同阶段选择性靶向炎症细胞和神经细胞的微环境自适应纳米颗粒(定制设计为带有狂犬病病毒糖蛋白29-RVG29和透明质酸-HA,RHNP)。数据表明,RHNP可以通过RVG29有效地穿过BSCB,并根据病理活性氧(ROS)信号通过二硒键选择性地暴露HA或RVG29来适应性地调节细胞内化。此外,将姜黄素加载到RHNP(RHNP-Cur)中以改善创伤性SCI小鼠模型中后肢的运动功能和协调性。本研究发现,RHNP-Cur对源自M1小胶质细胞/巨噬细胞和神经毒性星形胶质细胞的炎症级联反应具有抑制作用,并在神经再生过程中保护神经细胞免受炎症诱导的凋亡。总的来说,这项工作提供了一种微环境自适应纳米药物,能够对SCI进行有效的微创治疗。

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