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通过免疫调节微球桥接免疫-神经血管串扰以促进神经修复。

Bridging immune-neurovascular crosstalk via the immunomodulatory microspheres for promoting neural repair.

作者信息

Xu Tongtong, Gan Lin, Chen Wei, Zheng Dandan, Li Hanlai, Deng Shiyu, Qian Dongliang, Gu Tingting, Lian Qianyuan, Shen Gracie, An Qingzhu, Li Wanlu, Zhang Zhijun, Yang Guo-Yuan, Ruan Huitong, Cui Wenguo, Tang Yaohui

机构信息

Department of Orthopaedics and School of Biomedical Engineering, Shanghai Key Laboratory for Prevention and Treatment of Bone and Joint Diseases, Shanghai Institute of Traumatology and Orthopaedics, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai Jiao Tong University, 197 Ruijin 2nd Road, Shanghai, 200025, China.

Department of Neurosurgery, Huashan Hospital, Shanghai Medical School, Fudan University, 12 Wulumuqi Middle Road, Shanghai, 200040, China.

出版信息

Bioact Mater. 2024 Nov 8;44:558-571. doi: 10.1016/j.bioactmat.2024.10.031. eCollection 2025 Feb.

Abstract

The crosstalk between immune cells and the neurovascular unit plays a pivotal role in neural regeneration following central nervous system (CNS) injury. Maintaining brain immune homeostasis is crucial for restoring neurovascular function. In this study, an interactive bridge was developed via an immunomodulatory hydrogel microsphere to link the interaction network between microglia and the neurovascular unit, thereby precisely regulating immune-neurovascular crosstalk and achieving neural function recovery. This immunomodulatory crosstalk microsphere (MP/RIL4) was composed of microglia-targeted RAP12 peptide-modified interleukin-4 (IL-4) nanoparticles and boronic ester-functionalized hydrogel using biotin-avidin reaction and air-microfluidic techniques. We confirmed that the immunomodulatory microspheres reduced the expression of pro-inflammatory factors including IL-1β, iNOS, and CD86, while upregulating levels of anti-inflammatory factors such as IL-10, Arg-1, and CD206 in microglia. In addition, injection of the MP/RIL4 significantly mitigated brain atrophy volume in a mouse model of ischemic stroke, promoted neurobehavioral recovery, and enhanced the crosstalk between immune cells and the neurovascular unit, thus increasing angiogenesis and neurogenesis of stroke mice. In summary, the immunomodulatory microspheres, capable of orchestrating the interaction between immune cells and neurovascular unit, hold considerable therapeutic potential for ischemic stroke and other CNS diseases.

摘要

免疫细胞与神经血管单元之间的串扰在中枢神经系统(CNS)损伤后的神经再生中起关键作用。维持脑免疫稳态对于恢复神经血管功能至关重要。在本研究中,通过免疫调节水凝胶微球构建了一个交互桥梁,以连接小胶质细胞与神经血管单元之间的相互作用网络,从而精确调节免疫 - 神经血管串扰并实现神经功能恢复。这种免疫调节串扰微球(MP/RIL4)由靶向小胶质细胞的RAP12肽修饰的白细胞介素 - 4(IL - 4)纳米颗粒和使用生物素 - 抗生物素蛋白反应及空气微流控技术的硼酸酯功能化水凝胶组成。我们证实,免疫调节微球降低了包括IL - 1β、诱导型一氧化氮合酶(iNOS)和CD86在内的促炎因子的表达,同时上调了小胶质细胞中抗炎因子如IL - 10、精氨酸酶 - 1(Arg - 1)和CD206的水平。此外,在缺血性中风小鼠模型中注射MP/RIL4可显著减轻脑萎缩体积,促进神经行为恢复,并增强免疫细胞与神经血管单元之间的串扰,从而增加中风小鼠的血管生成和神经发生。总之,能够协调免疫细胞与神经血管单元之间相互作用的免疫调节微球对缺血性中风和其他中枢神经系统疾病具有巨大的治疗潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9939/11583666/32f4da2622a1/ga1.jpg

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