Shi Shengbo, Zhang Zijing, Shi Pengpeng, Gong Changsheng, Zhao Zetian, Wang Tienan, Zhou Yu, Zhang Meng, Gao Junxiao, Qin Song, Wang Jianchuan, Yu Xiaobing
Affiliated Zhongshan Hospital of Dalian University, No. 6 Jiefang Street, Zhongshan District, Dalian, Liaoning Province, 116001, People's Republic of China.
Shangqiu First People's Hospital, No. 292 Kaixuan South Road, Suiyang District, Shangqiu City, Henan Province, 476005, People's Republic of China.
Mol Neurobiol. 2025 Sep 5. doi: 10.1007/s12035-025-05164-1.
Spinal cord injury (SCI) is a severe traumatic disorder of the central nervous system, often resulting in partial or complete loss of sensory and motor functions. Ferroptosis, a lipid peroxidation-driven apoptotic process triggered by iron overload, has emerged as a novel form of programmed cell death and a focal point in post-SCI cell death research. Exosomes (Exo), as delivery vehicles, exhibit multiple advantages, including superior encapsulation capacity, high targeting efficiency, and enhanced blood-brain barrier penetration to reach the central nervous system. Previous studies have identified exosomes as key carriers of bioactive molecules, including miRNAs. Our prior investigations demonstrated that miR-494 attenuates SCI progression. To investigate the therapeutic mechanism of Exo-miR-494 in SCI, this study conducted in vitro and in vivo experiments using PC12 cell models and rat SCI models. In vitro, qRT-PCR and Western blot were employed to detect the expression levels of miR-494, SIRT1, HO-1, GPX4, and 4HNE, while intracellular oxidative stress markers were measured to clarify the regulatory effects of Exo-miR-494 on cellular oxidative stress and ferroptosis. In vivo, rats with successful SCI modeling were intravenously injected with Exo-miR-494. Fluorescence quantitative PCR, Western blot, and immunofluorescence were comprehensively used to analyze the changes in SIRT1/HO-1 signaling pathway molecules and ferroptosis-related indicators in injured spinal cord tissues. HE staining and Nissl staining were applied to evaluate spinal cord tissue damage and neuronal morphology. Transmission electron microscopy was utilized to observe cellular ultrastructural changes, and Prussian blue staining was combined to detect iron deposition, thereby deeply exploring the ferroptosis mechanism. Finally, Basso, Beattie, Bresnahan (BBB) locomotor scores and inclined plane tests were used to systematically assess the motor function recovery of rats. Results revealed a significant downregulation of miR-494 post-SCI. Exo-miR-494 effectively restored miR-494 levels in injured spinal tissues, suppressed ferroptosis through SIRT1/HO-1 pathway activation, mitigated SCI progression, and enhanced functional recovery in rats. Exosomes derived from rat bone marrow mesenchymal stem cells (BMSCs) delivering miR-494 represent a potential therapeutic strategy for SCI. miR-494 targets injury sites, reduces neuronal ferroptosis after spinal cord injury by regulating the SIRT1/HO-1 signaling pathway, alleviates damage caused by spinal cord injury, and promotes motor function recovery in rats.
脊髓损伤(SCI)是一种严重的中枢神经系统创伤性疾病,常导致感觉和运动功能部分或完全丧失。铁死亡是一种由铁过载引发的脂质过氧化驱动的凋亡过程,已成为一种新型的程序性细胞死亡形式,也是SCI后细胞死亡研究的焦点。外泌体(Exo)作为递送载体,具有多种优势,包括卓越的封装能力、高靶向效率以及增强的血脑屏障穿透能力以到达中枢神经系统。先前的研究已将外泌体确定为生物活性分子(包括miRNA)的关键载体。我们之前的研究表明,miR-494可减轻SCI的进展。为了研究Exo-miR-494在SCI中的治疗机制,本研究使用PC12细胞模型和大鼠SCI模型进行了体外和体内实验。在体外,采用qRT-PCR和蛋白质免疫印迹法检测miR-494、SIRT1、HO-1、GPX4和4HNE的表达水平,同时测量细胞内氧化应激标志物,以阐明Exo-miR-494对细胞氧化应激和铁死亡的调节作用。在体内,对成功建立SCI模型的大鼠静脉注射Exo-miR-494。综合运用荧光定量PCR、蛋白质免疫印迹法和免疫荧光分析损伤脊髓组织中SIRT1/HO-1信号通路分子和铁死亡相关指标的变化。应用苏木精-伊红(HE)染色和尼氏染色评估脊髓组织损伤和神经元形态。利用透射电子显微镜观察细胞超微结构变化,并结合普鲁士蓝染色检测铁沉积,从而深入探究铁死亡机制。最后,使用Basso、Beattie、Bresnahan(BBB)运动评分和倾斜平面试验系统评估大鼠的运动功能恢复情况。结果显示,SCI后miR-494显著下调。Exo-miR-494有效恢复了受损脊髓组织中miR-494的水平,通过激活SIRT1/HO-1途径抑制铁死亡,减轻SCI的进展,并增强大鼠的功能恢复。源自大鼠骨髓间充质干细胞(BMSC)的外泌体递送miR-494代表了一种治疗SCI的潜在策略。miR-494靶向损伤部位,通过调节SIRT1/HO-1信号通路减少脊髓损伤后神经元的铁死亡,减轻脊髓损伤造成的损害,并促进大鼠运动功能恢复。