Zhang Jinwei, Chen Xin, Du Kejun, Zhang Zhi, Ma Yuan, Kuang Yongqin, Yu Sixun, Shu Haifeng
Department of Neurosurgery, General Hospital of Western Theater Command of PLA, Chengdu, China.
Department of Neurosurgery, Sichuan Tianfu New Area People's Hospital, Chengdu, China.
PLoS One. 2025 Apr 15;20(4):e0321447. doi: 10.1371/journal.pone.0321447. eCollection 2025.
The recovery process from traumatic brain injury (TBI) is significantly impeded by inhibitors such as Nogo-A, myelin associated glycoprotein, and oligodendrocyte myelin glycoprotein, which exert an impact on the regeneration and repair of neuronal axons through their binding to Nogo-66 receptor 1 (NgR1). Recent research findings have revealed that NgR1 signaling may play a pivotal role in various seizure mechanisms, including the regulation of synaptic plasticity and migration of neural precursor cells. In this study, wild type (WT) and NgR1 knockout (KO) mice were utilized to establish craniocerebral injury models, while pentylenetetrazol (PTZ) was employed to induce seizures in both groups of mice following TBI. The results revealed that NgR1 KO mice exhibited heightened levels of neuronal electrical activity, along with elevated seizure scores compared to WT controls. Immunofluorescence staining demonstrated an increase in the number of excitatory synapses (P < 0.001) and a decrease in inhibitory synaptic density (P < 0.001) in NgR1 KO mice. Furthermore, the NgR1 KO model mice also displayed an augmentation in the number of presynaptic vesicles (P < 0.001), a narrowing of the synaptic gap (P < 0.001), and an elongation of the synaptic active region (P < 0.001). Our findings have demonstrated that in the previous single cognition of NgR1 inhibition in nerve function repair following TBI, revealing the potential risks associated with inhibiting NgR1 activity in nerve function repair following TBI, and providing a new perspective for understanding the role of NgR1 in the nervous system.
诸如Nogo-A、髓磷脂相关糖蛋白和少突胶质细胞髓磷脂糖蛋白等抑制因子会显著阻碍创伤性脑损伤(TBI)的恢复过程,这些抑制因子通过与Nogo-66受体1(NgR1)结合,对神经元轴突的再生和修复产生影响。最近的研究结果表明,NgR1信号传导可能在各种癫痫发作机制中起关键作用,包括对突触可塑性的调节和神经前体细胞的迁移。在本研究中,利用野生型(WT)和NgR1基因敲除(KO)小鼠建立颅脑损伤模型,同时在两组小鼠TBI后使用戊四氮(PTZ)诱导癫痫发作。结果显示,与WT对照组相比,NgR1基因敲除小鼠的神经元电活动水平升高,癫痫发作评分也升高。免疫荧光染色显示,NgR1基因敲除小鼠的兴奋性突触数量增加(P < 0.001),抑制性突触密度降低(P < 0.001)。此外,NgR1基因敲除模型小鼠的突触前囊泡数量也增加(P < 0.001),突触间隙变窄(P < 0.001),突触活性区域延长(P < 0.001)。我们的研究结果表明,以往对TBI后神经功能修复中NgR1抑制作用的单一认识存在局限性,揭示了TBI后神经功能修复中抑制NgR1活性的潜在风险,并为理解NgR1在神经系统中的作用提供了新的视角。