Li Xiao, Sun Xijuan, Xie Junning, Wan Hao
Psychosis Department 1, Qingdao Mental Health Center, Qingdao University, Qingdao 266034, PR China.
Open Mental Department, Qingdao Mental Health Center, Qingdao University, Qingdao 266034, PR China.
Brain Res. 2022 Jul 15;1787:147911. doi: 10.1016/j.brainres.2022.147911. Epub 2022 Apr 9.
Depression is an important mental disease that threatens human physical and mental health. Circular RNA (circRNA) has been confirmed to be involved in the regulation of depression progression, but the role and mechanism of circDYM in depression progression need to be further explored.
Chronic unpredictable mild stress (CUMS) mice model was constructed to assess mice depressive-like behavior using novelty-suppressed feeding test, sucrose preference test, social interaction test, and forced swimming test. The expression of circDYM, microRNA (miR)-497a-5p and glucocorticoid receptor (NR3C1) was measured by quantitative real-time PCR. The protein levels of NR3C1 and apoptosis markers were analyzed by western blot analysis. Hippocampal neurons viability, apoptosis and inflammation were detected by cell counting kit 8 assay, flow cytometry and ELISA assay. Furthermore, RNA interaction was confirmed by dual-luciferase reporter assay, RIP assay and RNA pull-down assay.
Our study showed that circDYM and NR3C1 were downregulated and miR-497a-5p was upregulated in the hippocampus tissues of CUMS mice. Overexpressed circDYM alleviated CUMS mice depressive-like behavior and repressed hippocampal neurons injury. In terms of mechanism, circDYM could upregulate NR3C1 by sponging miR-497a-5p. MiR-497a-5p overexpression reversed the regulation of circDYM on CUMS mice depressive-like behavior and hippocampal neurons injury. In addition, the function of miR-497a-5p overexpression on CUMS mice depressive-like behavior and hippocampal neurons injury also could be reversed by overexpressing NR3C1.
In summary, our study confirmed that circDYM could relieve the depressive-like behavior in CUMS mice and hippocampal neurons injury through miR-497a-5p/NR3C1 pathway. These data confirmed that circDYM had an anti-depressive function, which might be a potential target for depression treatment.
抑郁症是一种威胁人类身心健康的重要精神疾病。环状RNA(circRNA)已被证实参与抑郁症进展的调控,但circDYM在抑郁症进展中的作用及机制仍需进一步探索。
构建慢性不可预测性温和应激(CUMS)小鼠模型,采用新奇抑制摄食试验、蔗糖偏好试验、社会交互试验和强迫游泳试验评估小鼠的抑郁样行为。通过定量实时PCR检测circDYM、微小RNA(miR)-497a-5p和糖皮质激素受体(NR3C1)的表达。通过蛋白质免疫印迹分析检测NR3C1和凋亡标志物的蛋白水平。采用细胞计数试剂盒8法、流式细胞术和酶联免疫吸附测定法检测海马神经元活力、凋亡和炎症。此外,通过双荧光素酶报告基因试验、RNA免疫沉淀试验和RNA下拉试验证实RNA相互作用。
我们的研究表明,CUMS小鼠海马组织中circDYM和NR3C1表达下调,miR-497a-5p表达上调。过表达circDYM可减轻CUMS小鼠的抑郁样行为,并抑制海马神经元损伤。机制上,circDYM可通过海绵吸附miR-497a-5p上调NR3C1。miR-497a-5p过表达可逆转circDYM对CUMS小鼠抑郁样行为和海马神经元损伤的调控。此外,过表达NR3C1也可逆转miR-497a-5p过表达对CUMS小鼠抑郁样行为和海马神经元损伤的作用。
综上所述,我们的研究证实circDYM可通过miR-497a-5p/NR3C1途径缓解CUMS小鼠的抑郁样行为和海马神经元损伤。这些数据证实circDYM具有抗抑郁功能,可能是抑郁症治疗的潜在靶点。