Yuan Yajiang, Fan Xiangyi, Guo Zhanpeng, Zhou Zipeng, Gao Weiran
Department of Orthopedics, First Affiliated Hospital of Jinzhou Medical University, Jinzhou, China.
Department of Otolaryngology-Head and Neck Surgery, First Affiliated Hospital of Jinzhou Medical University, Jinzhou, China.
Anal Cell Pathol (Amst). 2022 Mar 27;2022:3634908. doi: 10.1155/2022/3634908. eCollection 2022.
Spinal cord injury (SCI) is an extreme neurological impairment with few effective drug treatments. Pyroptosis is a recently found and proven type of programmed cell death that is characterized by a reliance on inflammatory caspases and the release of a large number of proinflammatory chemicals. Pyroptosis differs from other cell death mechanisms such as apoptosis and necrosis in terms of morphological traits, incidence, and regulatory mechanism. Pyroptosis is widely involved in the occurrence and development of SCI. In-depth research on pyroptosis will help researchers better understand its involvement in the onset, progression, and prognosis of SCI, as well as provide new therapeutic prevention and treatment options. Herein, we investigated the role of AMPK-mediated activation of the NLRP3 inflammasome in the neuroprotection of MET-regulated pyroptosis. We found that MET treatment reduced NLRP3 inflammasome activation by activating phosphorylated AMPK and reduced proinflammatory cytokine (IL-1, IL-6, and TNF-) release. At the same time, MET improved motor function recovery in rats after SCI by reducing motor neuron loss in the anterior horn of the spinal cord. Taken together, our study confirmed that MET inhibits neuronal pyroptosis after SCI via the AMPK/NLRP3 signaling pathway, which is mostly dependent on the AMPK pathway increase, hence decreasing NLRP3 inflammasome activation.
脊髓损伤(SCI)是一种严重的神经功能障碍,有效的药物治疗方法很少。细胞焦亡是最近发现并得到证实的一种程序性细胞死亡类型,其特征是依赖炎性半胱天冬酶并释放大量促炎化学物质。细胞焦亡在形态特征、发生率和调节机制方面与其他细胞死亡机制(如凋亡和坏死)不同。细胞焦亡广泛参与SCI的发生和发展。对细胞焦亡的深入研究将有助于研究人员更好地理解其在SCI的发病、进展和预后中的作用,并提供新的治疗预防和治疗选择。在此,我们研究了AMPK介导的NLRP3炎性小体激活在MET调节的细胞焦亡神经保护中的作用。我们发现,MET治疗通过激活磷酸化AMPK降低了NLRP3炎性小体的激活,并减少了促炎细胞因子(IL-1、IL-6和TNF-)的释放。同时,MET通过减少脊髓前角运动神经元的损失,改善了SCI大鼠的运动功能恢复。综上所述,我们的研究证实,MET通过AMPK/NLRP3信号通路抑制SCI后神经元的细胞焦亡,这主要依赖于AMPK通路的增强,从而减少NLRP3炎性小体的激活。