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

被引:2
|
作者
Tang, Chunming [2 ]
Jin, Yaoyao [4 ]
Wu, Min [2 ]
Jia, Feng [5 ]
Lu, Xiaowei [6 ]
Li, Jinyu [2 ]
Wu, Jie [2 ]
Zhu, Senlin [2 ]
Wang, Zhiji [2 ]
An, Di [1 ]
Xiong, Wu [3 ]
Zhang, Yongjie [3 ]
Xu, Huae [2 ]
Chen, Xufeng [1 ]
机构
[1] Nanjing Med Univ, Affiliated Hosp 1, Dept Emergency Med, Nanjing 210029, Peoples R China
[2] Nanjing Med Univ, Sch Pharm, Dept Pharmaceut, Nanjing 211166, Peoples R China
[3] Nanjing Med Univ, Dept Human Anat, Nanjing 211166, Peoples R China
[4] Xuzhou Med Univ & Second Peoples Hosp Huaian, Affiliated Huaian Hosp, Dept Emergency, Huaian 223022, Peoples R China
[5] Nanjing Univ, Yancheng Peoples Hosp 1, Affiliated Yancheng Hosp 1, Dept Neurosurg,Med Sch, Yancheng 224008, Peoples R China
[6] Nanjing Med Univ, Affiliated Hosp 1, Dept Geriatr Neurol, Nanjing 210029, Peoples R China
关键词
Hybrid cell membrane; DNAse I conjugating; Neutrophil extracellular traps; Neutrophil hijacking; NF-kappa B; Spinal cord injury; METHYLPREDNISOLONE; INFLAMMATION; PROMOTE; DNA;
D O I
10.1016/j.mtbio.2024.101218
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
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 antiinflammatory 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-kappa B) pathway. We believe that the current study provides a new perspective for neuroinflammation inhibition and may shed new light on the treatment of SCI.
引用
收藏
页数:16
相关论文
共 39 条
  • [31] Interruption of neutrophil extracellular traps formation dictates host defense and tubular HOXA5 stability to augment efficacy of anti-Fn14 therapy against septic AKI
    Ni, Yin
    Hu, Bang-Chuan
    Wu, Guo-Hua
    Shao, Zi-Qiang
    Zheng, Yang
    Zhang, Run
    Jin, Jun
    Hong, Jun
    Yang, Xiang-Hong
    Sun, Ren-Hua
    Liu, Jin-Quan
    Mo, Shi-Jing
    THERANOSTICS, 2021, 11 (19): : 9431 - 9451
  • [32] Anti-Nogo-A Antibodies As a Potential Causal Therapy for Lower Urinary Tract Dysfunction after Spinal Cord Injury
    Schneider, Marc P.
    Sartori, Andrea M.
    Ineichen, Benjamin V.
    Moors, Selina
    Engmann, Anne K.
    Hofer, Anna-Sophie
    Weinmann, Oliver
    Kessler, Thomas M.
    Schwab, Martin E.
    JOURNAL OF NEUROSCIENCE, 2019, 39 (21) : 4066 - 4076
  • [33] Combined Activity-Based Therapy and Cervical Spinal Cord Stimulation: Active Ingredients, Targets and Mechanisms of Actions to Optimize Neurorestoration of Upper Limb Function After Cervical Spinal Cord Injury
    Gopaul, Urvashy
    Bayley, Mark Theodore
    Kalsi-Ryan, Sukhvinder
    PHYSIOTHERAPY RESEARCH INTERNATIONAL, 2025, 30 (02)
  • [34] Engineered extracellular vesicles derived from primary M2 macrophages with anti-inflammatory and neuroprotective properties for the treatment of spinal cord injury
    Chuanjie Zhang
    Daoyong Li
    Hengshuo Hu
    Zhe Wang
    Jinyu An
    Zhanshan Gao
    Kaihua Zhang
    Xifan Mei
    Chao Wu
    He Tian
    Journal of Nanobiotechnology, 19
  • [35] Engineered extracellular vesicles derived from primary M2 macrophages with anti-inflammatory and neuroprotective properties for the treatment of spinal cord injury
    Zhang, Chuanjie
    Li, Daoyong
    Hu, Hengshuo
    Wang, Zhe
    An, Jinyu
    Gao, Zhanshan
    Zhang, Kaihua
    Mei, Xifan
    Wu, Chao
    Tian, He
    JOURNAL OF NANOBIOTECHNOLOGY, 2021, 19 (01)
  • [36] A bioactive injectable self-healing anti-inflammatory hydrogel with ultralong extracellular vesicles release synergistically enhances motor functional recovery of spinal cord injury
    Wang, Chenggui
    Wang, Min
    Xia, Kaishun
    Wang, Jingkai
    Cheng, Feng
    Shi, Kesi
    Ying, Liwei
    Yu, Chao
    Xu, Haibin
    Xiao, Shining
    Liang, Chengzhen
    Li, Fangcai
    Lei, Bo
    Chen, Qixin
    BIOACTIVE MATERIALS, 2021, 6 (08) : 2523 - 2534
  • [37] Neural stem cell small extracellular vesicle-based delivery of 14-3-3t reduces apoptosis and neuroinflammation following traumatic spinal cord injury by enhancing autophagy by targeting Beclin-1
    Rong, Yuluo
    Liu, Wei
    Lv, Chengtang
    Wang, Jiaxing
    Luo, Yongjun
    Jiang, Dongdong
    Li, Linwei
    Zhou, Zheng
    Zhou, Wei
    Li, Qingqing
    Yin, Guoyong
    Yu, Lipeng
    Fan, Jin
    Cai, Weihua
    AGING-US, 2019, 11 (18): : 7723 - 7745
  • [38] Intravenous Administration of Mesenchymal Stem Cell-Derived Exosome Alleviates Spinal Cord Injury by Regulating Neutrophil Extracellular Trap Formation through Exosomal miR-125a-3p
    Morishima, Yutaka
    Kawabori, Masahito
    Yamazaki, Kazuyoshi
    Takamiya, Soichiro
    Yamaguchi, Sho
    Nakahara, Yo
    Senjo, Hajime
    Hashimoto, Daigo
    Masuda, Sakiko
    Fujioka, Yoichiro
    Ohba, Yusuke
    Mizuno, Yuki
    Kuge, Yuji
    Fujimura, Miki
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2024, 25 (04)
  • [39] Bone mesenchymal stem cell-derived extracellular vesicles deliver microRNA-23b to alleviate spinal cord injury by targeting toll-like receptor TLR4 and inhibiting NF-κB pathway activation
    Nie, Hongfei
    Jiang, Zhensong
    BIOENGINEERED, 2021, 12 (01) : 8157 - 8172