Chen Xi, Song Ying, Chen Guanghui, Zhang Baoliang, Bai Yang, Sun Chuiguo, Fan Dongwei, Chen Zhongqiang
Department of Orthopaedics, Peking University Third Hospital, Beijing 100191, China.
Beijing Key Laboratory of Spinal Disease Research, Beijing 100191, China.
Biomedicines. 2024 Mar 18;12(3):678. doi: 10.3390/biomedicines12030678.
Oxeiptosis is a reactive oxygen species (ROS)-induced pathway of cell death. The involvement of circular RNAs (circRNAs) has been confirmed in the incidence and progression of intervertebral disc degeneration (IVDD). However, whether oxeiptosis occurs in IVDD and how circRNAs regulate oxeiptosis is still unclear. In this study, we discovered that oxeiptosis could be induced in nucleus pulposus cells (NPCs), and circFOXO3 was significantly upregulated after oxeiptosis induction. Transfection using circFOXO3 small interfering RNA (siRNA) significantly inhibited oxeiptosis in NPCs. Mechanistically, circFOXO3 upregulated acid-sensing ion channel subunit 1 (ASIC1) expression by functioning as a molecular sponge for miR-185-3p and miR-939-5p. Subsequent rescue experiments validated that circFOXO3 could regulate oxeiptosis in NPCs via the miR-185-3p/miR-939-5p-ASIC1 axis. Further research on ASIC1 functions indicated that this regulation was achieved by affecting the Calcium ion (Ca) influx mediated by ASIC1. A mouse IVDD model was established, and silencing circFOXO3 in vivo was found to inhibit IVDD development and the activation of the oxeiptosis-related pathway. Overall, circFOXO3 is one of the factors contributing to the progression of IVDD by mediating oxeiptosis.
氧化应激诱导的细胞死亡(Oxeiptosis)是一种由活性氧(ROS)诱导的细胞死亡途径。环状RNA(circRNAs)在椎间盘退变(IVDD)的发生和发展中的作用已得到证实。然而,IVDD中是否发生氧化应激诱导的细胞死亡以及circRNAs如何调节氧化应激诱导的细胞死亡仍不清楚。在本研究中,我们发现髓核细胞(NPCs)中可诱导氧化应激诱导的细胞死亡,氧化应激诱导后circFOXO3显著上调。使用circFOXO3小干扰RNA(siRNA)转染可显著抑制NPCs中的氧化应激诱导的细胞死亡。机制上,circFOXO3通过作为miR-185-3p和miR-939-5p的分子海绵上调酸敏感离子通道亚基1(ASIC1)的表达。随后的拯救实验证实,circFOXO3可通过miR-185-3p/miR-939-5p-ASIC1轴调节NPCs中的氧化应激诱导的细胞死亡。对ASIC1功能的进一步研究表明,这种调节是通过影响ASIC1介导的钙离子(Ca)内流来实现的。建立了小鼠IVDD模型,发现体内沉默circFOXO3可抑制IVDD的发展和氧化应激诱导的细胞死亡相关途径的激活。总的来说,circFOXO3是通过介导氧化应激诱导的细胞死亡促进IVDD进展的因素之一。