Nie Xinyu, Liu Yanting, Yuan Tianyang, Yu Tong, Yun Zhihe, Xue Wu, Yu Tao, An Junyan, Dai Anyuan, Wu Kun, Liu Qinyi
Department of Orthopaedic, The second hospital of Jilin University, Changchun, China.
Department of Neurosurgery, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, South Korea.
J Nanobiotechnology. 2024 Jul 31;22(1):456. doi: 10.1186/s12951-024-02737-5.
Spinal cord injury (SCI) compromises the blood-spinal cord barrier (BSCB) and induces neuroinflammation, potentially exacerbating neuronal damage. This underscores the importance of maintaining BSCB integrity and mitigating neuroinflammation in SCI treatment. Our study explores an innovative approach to treating SCI by utilizing platelet-rich plasma-derived exosomes (PRP-Exos) to stabilize BSCB function and alleviate neuroinflammation. We successfully isolated exosomes from platelet-rich plasma and conducted both in vivo and in vitro experiments to assess the therapeutic effects of PRP-Exos and explore their potential mechanisms in stabilizing the BSCB, reducing neuroinflammation, and promoting neural functional recovery.In vitro results demonstrate that PRP-Exos significantly reduce the permeability of bEnd.3 cells under hypoxic-hypoglycemic conditions, thereby restoring the integrity of tight junctions. Additionally, our study elucidates the critical role of the NF-κB signaling pathway in the amelioration of neuroinflammation by PRP-Exos. In the SCI model, local injection of hydrogel-encapsulated PRP-Exos reduced Evans blue dye leakage, enhanced the expression of tight junction proteins, alleviated the inflammatory environment in the damaged area, and improved neural functional recovery. In conclusion, PRP-Exos presents a promising and effective treatment option for SCI.
脊髓损伤(SCI)会破坏血脊髓屏障(BSCB)并引发神经炎症,可能会加剧神经元损伤。这凸显了在脊髓损伤治疗中维持血脊髓屏障完整性和减轻神经炎症的重要性。我们的研究探索了一种创新的脊髓损伤治疗方法,即利用富含血小板血浆衍生的外泌体(PRP-Exos)来稳定血脊髓屏障功能并减轻神经炎症。我们成功地从富含血小板血浆中分离出外泌体,并进行了体内和体外实验,以评估PRP-Exos的治疗效果,并探索其在稳定血脊髓屏障、减轻神经炎症和促进神经功能恢复方面的潜在机制。体外实验结果表明,PRP-Exos在缺氧低血糖条件下能显著降低bEnd.3细胞的通透性,从而恢复紧密连接的完整性。此外,我们的研究阐明了NF-κB信号通路在PRP-Exos改善神经炎症中的关键作用。在脊髓损伤模型中,局部注射水凝胶包裹的PRP-Exos可减少伊文思蓝染料渗漏,增强紧密连接蛋白的表达,减轻损伤区域的炎症环境,并改善神经功能恢复。总之,PRP-Exos为脊髓损伤提供了一种有前景且有效的治疗选择。