Jiangsu Province Key Laboratory of Anesthesiology, Xuzhou Medical University, Xuzhou 221004, China,
Jiangsu Province Key Laboratory of Anesthesia and Analgesia Application Technology, Xuzhou Medical University, Xuzhou 221004, China, and.
J Neurosci. 2019 Mar 13;39(11):2125-2143. doi: 10.1523/JNEUROSCI.1631-18.2018. Epub 2019 Jan 16.
Dysfunctions of gene transcription and translation in the nociceptive pathways play the critical role in development and maintenance of chronic pain. Circular RNAs (circRNAs) are emerging as new players in regulation of gene expression, but whether and how circRNAs are involved in chronic pain remain elusive. We showed here that complete Freund's adjuvant-induced chronic inflammation pain significantly increased circRNA-Filip1l (filamin A interacting protein 1-like) expression in spinal neurons of mice. Blockage of this increase attenuated complete Freund's adjuvant-induced nociceptive behaviors, and overexpression of spinal circRNA-Filip1l in naive mice mimicked the nociceptive behaviors as evidenced by decreased thermal and mechanical nociceptive threshold. Furthermore, we found that mature circRNA-Filip1l expression was negatively regulated by miRNA-1224 via binding and splicing of precursor of circRNA-Filip1l (pre-circRNA-Filip1l) in the Argonaute-2 ()-dependent manner. Increase of spinal circRNA-Filip1l expression resulted from the decrease of miRNA-1224 expression under chronic inflammation pain state. miRNA-1224 knockdown or overexpression induced nociceptive behaviors in naive mice, which was prevented by the knockdown of spinal circRNA-Filip1l. Finally, we demonstrated that a ubiquitin protein ligase E3 component -recognin 5 (), validated as a target of circRNA-Filip1l, plays a pivotal role in regulation of nociception by spinal circRNA-Filip1l. These data suggest that miRNA-1224-mediated and Ago2-dependent modulation of spinal circRNA-Filip1l expression regulates nociception via targeting , revealing a novel epigenetic mechanism of interaction between miRNA and circRNA in chronic inflammation pain. circRNAs are emerging as new players in regulation of gene expression. Here, we found that the increase of circRNA-Filip1l mediated by miRNA-1224 in an Ago2-dependent way in the spinal cord is involved in regulation of nociception via targeting Our study reveals a novel epigenetic mechanism of interaction between miRNA and circRNA in chronic inflammation pain.
基因转录和翻译功能障碍在伤害性通路中发挥关键作用,参与慢性疼痛的发生和维持。环状 RNA(circRNA)作为基因表达调控的新成员不断涌现,但 circRNA 是否以及如何参与慢性疼痛仍不清楚。我们在这里表明,完全弗氏佐剂诱导的慢性炎症疼痛显著增加了小鼠脊髓神经元中环状 RNA-Filip1l(细丝蛋白 A 相互作用蛋白 1 样)的表达。阻断这种增加可减轻完全弗氏佐剂诱导的痛觉行为,而在正常小鼠中过表达脊髓环状 RNA-Filip1l 可模拟痛觉行为,表现为热和机械痛觉阈值降低。此外,我们发现成熟的 circRNA-Filip1l 表达受 miRNA-1224 的负调控,通过结合和剪接 circRNA-Filip1l 的前体(pre-circRNA-Filip1l),该过程依赖于 Argonaute-2(AGO2)。在慢性炎症疼痛状态下,circRNA-Filip1l 表达的增加是由于 miRNA-1224 表达的减少。脊髓内 miRNA-1224 敲低或过表达可在正常小鼠中诱导痛觉行为,而脊髓 circRNA-Filip1l 的敲低可阻止这种行为。最后,我们证明一种泛素蛋白连接酶 E3 成分识别蛋白 5(UBR5),验证为 circRNA-Filip1l 的靶标,在通过脊髓 circRNA-Filip1l 调节痛觉中起关键作用。这些数据表明,miRNA-1224 介导的和 Ago2 依赖性的脊髓 circRNA-Filip1l 表达调节通过靶向 ,通过靶向 ,调节 nociception。我们的研究揭示了慢性炎症疼痛中 miRNA 和 circRNA 之间相互作用的新表观遗传机制。circRNA 作为基因表达调控的新成员不断涌现。在这里,我们发现 miRNA-1224 依赖 Ago2 在脊髓中增加 circRNA-Filip1l 的表达,通过靶向 参与调节 nociception。我们的研究揭示了慢性炎症疼痛中 miRNA 和 circRNA 之间相互作用的新表观遗传机制。