长链非编码 RNA NR3C2-8:1 通过 miR-129-5p/USP10 轴促进肌萎缩侧索硬化症中 p53 介导的细胞凋亡。
The Long Non-Coding RNA NR3C2-8:1 Promotes p53-Mediated Apoptosis through the miR-129-5p/USP10 Axis in Amyotrophic Lateral Sclerosis.
机构信息
Department of Neurology, Laboratory of Neurodegenerative Disorders, National Clinical Research Center for Geriatrics, West China Hospital, Sichuan University, No.37, Guoxue Lane, Chengdu, Sichuan, 610041, China.
Department of Neurosurgery, West China Hospital, Sichuan University, No.37, Guoxue Lane, Chengdu, Sichuan, 610041, China.
出版信息
Mol Neurobiol. 2024 Oct;61(10):7466-7480. doi: 10.1007/s12035-024-04059-x. Epub 2024 Feb 23.
Motor neuron degeneration in amyotrophic lateral sclerosis (ALS) is a form of apoptosis, but the mechanisms underlying this neuronal cell death remain unclear. Numerous studies demonstrate abnormally elevated and active p53 in the central nervous system of ALS patients. Activation of p53-regulated pro-apoptotic signaling pathways may trigger motor neuron death. We previously reported decreased expression of the long non-coding RNA NR3C2-8:1 (Lnc-NR3C) in leukocytes of ALS patients. Here, we show lnc-NR3C promotes p53-mediated cell death in ALS by upregulating USP10 and promoting lnc-NR3C-triggered p53 activation, resulting in cell death. Conversely, lnc-NR3C knockdown inhibited USP10-triggered p53 activation, thereby protecting cells against oxidative stress. As a competitive endogenous RNA, lnc-NR3C competitively binds miR-129-5p, regulating the usp10/p53 axis. Elucidating the link between Lnc-NR3C and the USP10/p53 axis in an ALS cell model reveals a role for long non-coding RNAs in activating apoptosis. This provides new therapeutic opportunities in ALS.
肌萎缩侧索硬化症(ALS)中的运动神经元退化是一种细胞凋亡形式,但这种神经元细胞死亡的机制仍不清楚。许多研究表明,ALS 患者的中枢神经系统中 p53 异常升高且活跃。p53 调节的促凋亡信号通路的激活可能引发运动神经元死亡。我们之前报道了 ALS 患者白细胞中长链非编码 RNA NR3C2-8:1 (Lnc-NR3C) 的表达降低。在这里,我们显示 Lnc-NR3C 通过上调 USP10 并促进 Lnc-NR3C 触发的 p53 激活来促进 ALS 中的 p53 介导的细胞死亡,从而导致细胞死亡。相反,Lnc-NR3C 敲低抑制了 USP10 触发的 p53 激活,从而保护细胞免受氧化应激。作为一种竞争性内源性 RNA,Lnc-NR3C 竞争性结合 miR-129-5p,调节 USP10/p53 轴。阐明 ALS 细胞模型中 Lnc-NR3C 与 USP10/p53 轴之间的联系揭示了长非编码 RNA 在激活细胞凋亡中的作用。这为 ALS 提供了新的治疗机会。