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Hsa_circ_0002468 通过调控 miR-561/E2F8 轴调控 SH-SY5Y 细胞的神经元分化。

Hsa_circ_0002468 Regulates the Neuronal Differentiation of SH-SY5Y Cells by Modulating the MiR-561/E2F8 Axis.

机构信息

Department of Neurology, Central South University Xiangya School of Medicine Affiliated Haikou Hospital, Haikou, Hainan, China (mainland).

Department of Neurology, The Second People's Hospital of Hunan Province, Changsha, Hunan, China (mainland).

出版信息

Med Sci Monit. 2019 Apr 5;25:2511-2519. doi: 10.12659/MSM.915518.

Abstract

BACKGROUND It has been shown that circular RNAs (circRNAs) play a vital role in the regulation of neuronal differentiation; however, the precise role of circRNAs in human neuronal differentiation remains largely unexplored. MATERIAL AND METHODS A dual-luciferase reporter assay was carried out to confirm the targets of hsa_circ_0002468, miR-561, E2F8 (E2F transcription factor 8, a protein coding gene), and miR-561. We detected the expression of hsa_circ_0002468, miR-561, and E2F8 by using quantitative real-time polymerase chain reaction (qRT-PCR) analyses. In addition, we performed the functional experiments by using a BrdU (5-bromo-2'-deoxyuridine) assay and qRT-PCR analyses. RESULTS In this study, we showed that hsa_circ_0002468 can act as a sponge of miR-561 to regulate SH-SY5Y proliferation and differentiation. A bioinformatics analysis showed that hsa_circ_0002468 had a binding site that corresponded to miR-561, which was verified by dual-luciferase reporter assay. The expression of hsa_circ_0002468 was increased during SH-SY5Y differentiation and was inversely correlated with miR-561 expression. Using qRT-PCR analysis, we showed that hsa_circ_0002468 negatively regulated miR-561 in SH-SY5Y cells. Intriguingly, the overexpression of hsa_circ_0002468 increased SH-SY5Y differentiation and reduced SH-SY5Y proliferation; the suppression of hsa_circ_0002468 led to decreased SH-SY5Y differentiation levels and increased SH-SY5Y proliferation levels. Additionally, overexpression of miR-561 rescued the SH-SY5Y proliferation deficiency induced by hsa_circ_0002468 overexpression and abolished the SH-SY5Y differentiation promoted by hsa_circ_0002468. Furthermore, E2F8 was validated as a direct target of miR-561. CONCLUSIONS Our data suggested that hsa_circ_0002468 was a novel circRNA that regulated SH-SY5Y cell proliferation and differentiation via targeting the miR-561/E2F8 axis. Therefore, manipulating hsa_circ_0002468 in SH-SY5Y cells could be a novel strategy to develop novel interventions for the treatment of relevant neurological disorders.

摘要

背景

已经表明环状 RNA(circRNAs)在神经元分化的调控中发挥着重要作用;然而,circRNAs 在人类神经元分化中的精确作用在很大程度上仍未被探索。

材料与方法

进行了双荧光素酶报告基因实验以验证 hsa_circ_0002468、miR-561、E2F8(E2F 转录因子 8,一种蛋白编码基因)和 miR-561 的靶标。我们使用实时定量聚合酶链反应(qRT-PCR)分析检测了 hsa_circ_0002468、miR-561 和 E2F8 的表达。此外,我们通过 BrdU(5-溴-2'-脱氧尿苷)测定和 qRT-PCR 分析进行了功能实验。

结果

在这项研究中,我们表明 hsa_circ_0002468 可以作为 miR-561 的海绵,调节 SH-SY5Y 的增殖和分化。生物信息学分析表明 hsa_circ_0002468 具有与 miR-561 对应的结合位点,该结合位点通过双荧光素酶报告基因实验得到了验证。hsa_circ_0002468 在 SH-SY5Y 分化过程中表达增加,与 miR-561 的表达呈负相关。通过 qRT-PCR 分析,我们表明 hsa_circ_0002468 在 SH-SY5Y 细胞中负调控 miR-561。有趣的是,hsa_circ_0002468 的过表达增加了 SH-SY5Y 的分化并减少了 SH-SY5Y 的增殖;hsa_circ_0002468 的抑制导致 SH-SY5Y 分化水平降低和增殖水平升高。此外,miR-561 的过表达挽救了 hsa_circ_0002468 过表达引起的 SH-SY5Y 增殖缺陷,并消除了 hsa_circ_0002468 促进的 SH-SY5Y 分化。此外,E2F8 被验证为 miR-561 的直接靶标。

结论

我们的数据表明,hsa_circ_0002468 是一种新型 circRNA,通过靶向 miR-561/E2F8 轴调节 SH-SY5Y 细胞的增殖和分化。因此,在 SH-SY5Y 细胞中操纵 hsa_circ_0002468 可能是开发治疗相关神经障碍的新干预措施的一种新策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/667a/6462173/c8ce35334ca0/medscimonit-25-2511-g001.jpg

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