Wang Shu-Chao, Hu Xi-Min, Xiong Kun
Center for Medical Research, The Second Xiangya Hospital of Central South University; Department of Anatomy and Neurobiology, School of Basic Medical Sciences, Central South University, Changsha, Hunan Province, China.
Department of Anatomy and Neurobiology, School of Basic Medical Sciences, Central South University, Changsha, Hunan Province, China.
Neural Regen Res. 2023 Jan;18(1):74-80. doi: 10.4103/1673-5374.341043.
Regulated cell death predominantly involves apoptosis, autophagy, and regulated necrosis. It is vital that we understand how key regulatory signals can control the process of cell death. Pin1 is a cis-trans isomerase that catalyzes the isomerization of phosphorylated serine or threonine-proline motifs of a protein, thereby acting as a crucial molecular switch and regulating the protein functionality and the signaling pathways involved. However, we know very little about how Pin1-associated pathways might play a role in regulated cell death. In this paper, we review the role of Pin1 in regulated cell death and related research progress and summarize Pin1-related pathways in regulated cell death. Aside from the involvement of Pin1 in the apoptosis that accompanies neurodegenerative diseases, accumulating evidence suggests that Pin1 also plays a role in regulated necrosis and autophagy, thereby exhibiting distinct effects, including both neurotoxic and neuroprotective effects. Gaining an enhanced understanding of Pin1 in neuronal death may provide us with new options for the development of therapeutic target for neurodegenerative disorders.
程序性细胞死亡主要涉及细胞凋亡、自噬和程序性坏死。了解关键调控信号如何控制细胞死亡过程至关重要。Pin1是一种顺反异构酶,可催化蛋白质磷酸化丝氨酸或苏氨酸 - 脯氨酸基序的异构化,从而作为关键的分子开关,调节蛋白质功能和相关信号通路。然而,我们对Pin1相关途径如何在程序性细胞死亡中发挥作用知之甚少。在本文中,我们综述了Pin1在程序性细胞死亡中的作用及相关研究进展,并总结了程序性细胞死亡中与Pin1相关的途径。除了Pin1参与神经退行性疾病伴随的细胞凋亡外,越来越多的证据表明Pin1在程序性坏死和自噬中也发挥作用,从而表现出不同的效应,包括神经毒性和神经保护作用。深入了解Pin1在神经元死亡中的作用可能为我们开发神经退行性疾病治疗靶点提供新的选择。