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lncRNA-SNHG14 通过海绵 miR-19a-3p 调控 ROR 表达促进动脉粥样硬化。

lncRNA-SNHG14 Promotes Atherosclerosis by Regulating ROR Expression through Sponge miR-19a-3p.

机构信息

Department of Physiology, Jining Medical College, Jining, Shandong, China.

Department of Pharmacy, Jining Medical College, Jining, Shandong, China.

出版信息

Comput Math Methods Med. 2020 Aug 25;2020:3128053. doi: 10.1155/2020/3128053. eCollection 2020.

DOI:10.1155/2020/3128053
PMID:32908577
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7468621/
Abstract

Coronary heart disease (CHD) is the most common cardiovascular disease with high prevalence, disability, and mortality. The balance between proliferation and apoptosis of vascular smooth muscle cells (VSMCs) plays a key role in the initiation of atherosclerosis. In this study, we found a significant decrease in the expression of lncRNA-SNHG14 in atherosclerotic plaque tissues of ApoE-/- mice. Overexpression of lncRNA-SNHG14 can inhibit VSMC proliferation while promoting apoptosis. There is a potential reciprocal regulatory relationship between lncRNASNHG14 and miR-19a-3p, which inhibit each other's expression in vascular smooth muscle cells. In addition, the luciferase reporter gene analysis results showed that there was a direct interaction between miR-19a-3p and the 3'UTR of ROR. The results of qRT-PCR showed that the level of ROR mRNA was significantly increased in the aortas treated with miR-19a-3p and SNHG14 compared with that treated with miR-19a-3p alone. In conclusion, we demonstrated that lncRNA-SNHG14 regulates the apoptosis/proliferation balance of VSMCs in atherosclerosis.

摘要

冠心病(CHD)是最常见的心血管疾病,具有高患病率、高致残率和高死亡率。血管平滑肌细胞(VSMCs)的增殖和凋亡平衡在动脉粥样硬化的发生中起着关键作用。在本研究中,我们发现载脂蛋白 E 基因敲除(ApoE-/-)小鼠动脉粥样硬化斑块组织中 lncRNA-SNHG14 的表达显著降低。lncRNA-SNHG14 的过表达可以抑制 VSMC 的增殖,同时促进其凋亡。lncRNA-SNHG14 和 miR-19a-3p 之间存在潜在的相互调节关系,它们在血管平滑肌细胞中相互抑制表达。此外,荧光素酶报告基因分析结果表明 miR-19a-3p 与 ROR 的 3'UTR 之间存在直接相互作用。qRT-PCR 结果显示,与单独转染 miR-19a-3p 相比,转染 miR-19a-3p 和 SNHG14 可使主动脉中 ROR mRNA 的水平显著升高。综上所述,我们证明了 lncRNA-SNHG14 调节动脉粥样硬化中 VSMCs 的凋亡/增殖平衡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7231/7468621/cbed5eb22278/CMMM2020-3128053.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7231/7468621/f5bf8c17d781/CMMM2020-3128053.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7231/7468621/2776bbeaf651/CMMM2020-3128053.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7231/7468621/8f184f4acf87/CMMM2020-3128053.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7231/7468621/535088465aab/CMMM2020-3128053.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7231/7468621/cbed5eb22278/CMMM2020-3128053.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7231/7468621/f5bf8c17d781/CMMM2020-3128053.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7231/7468621/2776bbeaf651/CMMM2020-3128053.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7231/7468621/8f184f4acf87/CMMM2020-3128053.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7231/7468621/535088465aab/CMMM2020-3128053.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7231/7468621/cbed5eb22278/CMMM2020-3128053.005.jpg

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