LncRNA GAS5 promotes epilepsy progression through the epigenetic repression of miR-219, in turn affecting CaMKIIγ/NMDAR pathway

IF 1.8 4区 医学 Q3 GENETICS & HEREDITY Journal of neurogenetics Pub Date : 2022-01-02 DOI:10.1080/01677063.2022.2067536
Chen-sheng Zhao, Dong-xing Liu, Yanping Fan, Jian-kun Wu
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引用次数: 4

Abstract

Abstract It has been widely reported that dysregulated long-chain noncoding RNAs (lncRNAs) are closely associated with epilepsy. This study aimed to probe the function of lncRNA growth arrest-specific 5 (GAS5), microRNA (miR)-219 and Calmodulin-dependent protein kinase II (CaMKII)γ/N-methyl-D-aspartate receptor (NMDAR) pathway in epilepsy. Epileptic cell and animal models were constructed using magnesium deficiency treatment and diazepam injection, respectively. GAS5 and miR-219 expressions in epileptic cell and animal models were determined using qRT-PCR assay. The protein levels of CaMKIIγ, NMDAR and apoptosis-related proteins levels were assessed by western blot. Cell counting kit-8 (CCK-8) assay was employed to determine cell proliferation. Besides, TNFα, IL-1β, IL-6 and IL-8 levels were analyzed using enzyme-linked immunosorbent assay (ELISA). Furthermore, cell apoptosis was evaluated using TUNEL staining and flow cytometric analysis. Finally, the binding relationship between GAS5 and EZH2 was verified using RIP and ChIP assay. Our results revealed that GAS5 was markedly upregulated in epileptic cell and animal models, while miR-219 was down-regulated. GAS5 knockdown dramatically increased cell proliferation of epileptic cells, whereas suppressed inflammation and the apoptosis. Furthermore, our results showed that GAS5 epigenetically suppressed transcriptional miR-219 expression via binding to EZH2. miR-219 mimics significantly enhanced cell proliferation of epileptic cells, while inhibited inflammation and the apoptosis, which was neutralized by CaMKIIγ overexpression. Finally, miR-219 inhibition reversed the effects of GAS5 silence on epileptic cells, which was eliminated by CaMKIIγ inhibition. In conclusion, GAS5 affected inflammatory response and cell apoptosis of epilepsy via inhibiting miR-219 and further regulating CaMKIIγ/NMDAR pathway (See graphic summary in Supplementary Material).
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LncRNA GAS5通过miR-219的表观遗传学抑制促进癫痫进展,进而影响CaMKIIγ/NDAR通路
摘要广泛报道,失调的长链非编码RNA(lncRNA)与癫痫密切相关。本研究旨在探讨lncRNA生长停滞特异性5(GAS5)、微小RNA(miR)-219和钙调蛋白依赖性蛋白激酶II(CaMKII)γ/N-甲基-D-天冬氨酸受体(NMDAR)通路在癫痫中的作用。分别使用镁缺乏治疗和安定注射液构建癫痫细胞和动物模型。使用qRT-PCR测定癫痫细胞和动物模型中GAS5和miR-219的表达。免疫印迹法检测CaMKIIγ、NMDAR蛋白水平及细胞凋亡相关蛋白水平。细胞计数试剂盒-8(CCK-8)测定法用于测定细胞增殖。采用酶联免疫吸附试验(ELISA)测定TNFα、IL-1β、IL-6和IL-8水平。此外,使用TUNEL染色和流式细胞术分析来评估细胞凋亡。最后,使用RIP和ChIP分析验证了GAS5和EZH2之间的结合关系。我们的研究结果显示,GAS5在癫痫细胞和动物模型中显著上调,而miR-219则下调。GAS5基因敲除显著增加癫痫细胞的增殖,同时抑制炎症和细胞凋亡。此外,我们的研究结果表明,GAS5通过与EZH2结合,表观遗传学抑制转录miR-219的表达。miR-219模拟显著增强癫痫细胞的细胞增殖,同时抑制炎症和细胞凋亡,这被CaMKIIγ过表达所中和。最后,miR-219的抑制逆转了GAS5沉默对癫痫细胞的影响,这种影响被CaMKIIγ的抑制所消除。总之,GAS5通过抑制miR-219和进一步调节CaMKIIγ/NDAR途径影响癫痫的炎症反应和细胞凋亡(见补充材料中的图形摘要)。
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来源期刊
Journal of neurogenetics
Journal of neurogenetics 医学-神经科学
CiteScore
4.40
自引率
0.00%
发文量
13
审稿时长
>12 weeks
期刊介绍: The Journal is appropriate for papers on behavioral, biochemical, or cellular aspects of neural function, plasticity, aging or disease. In addition to analyses in the traditional genetic-model organisms, C. elegans, Drosophila, mouse and the zebrafish, the Journal encourages submission of neurogenetic investigations performed in organisms not easily amenable to experimental genetics. Such investigations might, for instance, describe behavioral differences deriving from genetic variation within a species, or report human disease studies that provide exceptional insights into biological mechanisms
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