Department of Neurology, The First People's Hospital of Wenling, Wenling, Zhejiang, China.
Department of Neurology, The First People's Hospital of Wenling, Wenling, Zhejiang, China.
Biochem Biophys Res Commun. 2020 Feb 5;522(2):388-394. doi: 10.1016/j.bbrc.2019.11.102. Epub 2019 Nov 21.
Parkinson's disease (PD) is a neurodegenerative disease which is characterized by the substantia nigra dopaminergic neurons denatured. Circular RNA (circRNA) DLGAP4 (circDLGAP4) was found to have neuroprotective effect. In this study, we aimed to investigate whether circDLGAP4 participates in the progression of PD. Here, our results showed that circDLGAP4 expression was decreased in MPTP-induced PD mouse model and MPP-induced PD cell models. In vitro study revealed that circDLGAP4 could promote viability, reduce apoptosis, decrease mitochondrial damage, enhance autophagy and thereby attenuated the neurotoxic effects of MPP in SH-SY5Y and MN9D cells. Further research suggested that circDLGAP4 exerted its functions via regulating miR-134-5p. Moreover, we demonstrated that CREB was a target of miR-134-5p and CREB expression could be regulated by circDLGAP4/miR-134-5p axis. CircDLGAP4/miR-134-5p could also modulate the activation of CREB signaling and thereby influence the expression of CREB target genes including BDNF, Bcl-2 and PGC-1α in SH-SY5Y and MN9D cells. In all, our study identifies that circDLGAP4 exerts neuroprotective effects via modulating miR-134-5p/CREB pathway both in human and mouse.
帕金森病(PD)是一种神经退行性疾病,其特征是黑质多巴胺能神经元变性。环状 RNA(circRNA)DLGAP4(circDLGAP4)被发现具有神经保护作用。在本研究中,我们旨在研究 circDLGAP4 是否参与 PD 的进展。研究结果表明,MPTP 诱导的 PD 小鼠模型和 MPP 诱导的 PD 细胞模型中 circDLGAP4 的表达降低。体外研究表明,circDLGAP4 可以促进细胞活力,减少细胞凋亡,减少线粒体损伤,增强自噬,从而减轻 MPP 对 SH-SY5Y 和 MN9D 细胞的神经毒性作用。进一步的研究表明,circDLGAP4 通过调节 miR-134-5p 发挥作用。此外,我们证明 CREB 是 miR-134-5p 的靶基因,并且 CREB 的表达可以通过 circDLGAP4/miR-134-5p 轴进行调节。circDLGAP4/miR-134-5p 还可以调节 CREB 信号的激活,从而影响包括 BDNF、Bcl-2 和 PGC-1α 在内的 CREB 靶基因在 SH-SY5Y 和 MN9D 细胞中的表达。总之,我们的研究表明 circDLGAP4 通过调节 miR-134-5p/CREB 通路在人和小鼠中发挥神经保护作用。