Li Dachuan, Liu Siyang, Lu Xiao, Gong Zhaoyang, Wang Hongli, Xia Xinlei, Lu Feizhou, Jiang Jianyuan, Zhang Yuxuan, Xu Guangyu, Zou Fei, Ma Xiaosheng
Department of Orthopedics, Huashan Hospital, Fudan University, Shanghai, China.
CNS Neurosci Ther. 2024 Dec;30(12):e70130. doi: 10.1111/cns.70130.
The treatment of spinal cord injury (SCI) is usually ineffective, because neuroinflammatory secondary injury is an important cause of the continuous development of spinal cord injury, and microglial pyroptosis is an important step of neuroinflammation. Recently, Bmal1, a core component of circadian clock genes (CCGs), has been shown to play a regulatory role in various tissues and cells. However, it is still unclear whether Bmal1 regulates microglial pyroptosis after SCI.
In this study, we established an in vivo mouse model of SCI using Bmal1 knockout (KO) mice and wild-type (WT) mice, and lipopolysaccharide (LPS)-induced pyroptosis in BV2 cells as an in vitro model. A series of molecular and histological methods were used to detect the level of pyroptosis and explore the regulatory mechanism in vivo and in vitro respectively.
Both in vitro and in vivo results showed that Bmal1 inhibited NLRP3 inflammasome activation and microglial pyroptosis after SCI. Further analysis showed that Bmal1 inhibited pyroptosis-related proteins (NLRP3, Caspase-1, ASC, GSDMD-N) and reduced the release of IL-18 and IL-1β by inhibiting the NF-κB /MMP9 pathway. It was important that NF-κB was identified as a transcription factor that promotes the expression of MMP9, which in turn regulates microglial pyroptosis after SCI.
Our study initially identified that Bmal1 regulates the NF-κB /MMP9 pathway to reduce microglial pyroptosis and thereby reduce secondary spinal cord injury, providing a new promising therapeutic target for SCI.
脊髓损伤(SCI)的治疗通常效果不佳,因为神经炎症继发性损伤是脊髓损伤持续发展的重要原因,而小胶质细胞焦亡是神经炎症的重要环节。近来,生物钟基因(CCGs)的核心成分Bmal1已被证实在多种组织和细胞中发挥调节作用。然而,Bmal1是否在脊髓损伤后调节小胶质细胞焦亡仍不清楚。
在本研究中,我们使用Bmal1基因敲除(KO)小鼠和野生型(WT)小鼠建立了脊髓损伤的体内小鼠模型,并以脂多糖(LPS)诱导BV2细胞焦亡作为体外模型。分别采用一系列分子和组织学方法检测焦亡水平,并在体内和体外探索调节机制。
体外和体内结果均显示,Bmal1在脊髓损伤后抑制NLRP3炎性小体激活和小胶质细胞焦亡。进一步分析表明,Bmal1通过抑制NF-κB/MMP9途径抑制焦亡相关蛋白(NLRP3、Caspase-1、ASC、GSDMD-N),并减少IL-18和IL-1β的释放。重要的是,NF-κB被确定为促进MMP9表达的转录因子,进而在脊髓损伤后调节小胶质细胞焦亡。
我们的研究初步确定,Bmal1通过调节NF-κB/MMP9途径减少小胶质细胞焦亡,从而减轻脊髓继发性损伤,为脊髓损伤提供了一个有前景的新治疗靶点。