Institute of Chronic Disease Risks Assessment, Henan University, Jinming Avenue, Kaifeng, 475004, China.
School of Basic Medical Sciences, Henan University, Kaifeng, 475004, Henan, China.
Mol Neurobiol. 2024 Mar;61(3):1271-1281. doi: 10.1007/s12035-023-03614-2. Epub 2023 Sep 12.
Autophagy is a conservative self-degradation system, which includes the two major processes of enveloping abnormal proteins, organelles and other macromolecules, and transferring them into lysosomes for the subsequent degradation. It holds the stability of the intracellular environment under stress. So far, three types of autophagy have been found: microautophagy, chaperone-mediated autophagy and macroautophagy. Many diseases have the pathological process of autophagy dysfunction, such as nervous system diseases. Pyroptosis is one kind of programmed cell death mediated by gasdermin (GSDM). In this process of pyroptosis, the activated caspase-3, caspase-4/5/11, or caspase-1 cleaves GSDM into the N-terminal pore-forming domain (PFD). The oligomer of PFD combines with the cell membrane to form membrane holes, thus leading to pyroptosis. Pyroptosis plays a key role in multiple tissues and organs. Many studies have revealed that autophagy and pyroptosis participate in the nervous system, but the mechanisms need to be fully clarified. Here, we focused on the recent articles on the role and mechanism of pyroptosis and autophagy in the pathological processes of the nervous system.
自噬是一种保守的自我降解系统,它包括两个主要过程:包裹异常蛋白质、细胞器和其他大分子,并将它们转移到溶酶体中进行后续降解。它在压力下维持细胞内环境的稳定性。迄今为止,已经发现了三种自噬:微自噬、伴侣介导的自噬和巨自噬。许多疾病的病理过程都与自噬功能障碍有关,如神经系统疾病。细胞焦亡是一种由 gasdermin (GSDM) 介导的程序性细胞死亡。在这个细胞焦亡过程中,激活的 caspase-3、caspase-4/5/11 或 caspase-1 将 GSDM 切割成 N 端孔形成结构域 (PFD)。PFD 的寡聚体与细胞膜结合形成膜孔,从而导致细胞焦亡。细胞焦亡在多个组织和器官中发挥关键作用。许多研究表明,自噬和细胞焦亡参与神经系统,但需要充分阐明其机制。在这里,我们重点关注了最近关于细胞焦亡和自噬在神经系统病理过程中的作用和机制的文章。