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氧化型低密度脂蛋白诱导的 ASMC 失调依赖于 circ_0000345 介导的调控机制。

Oxygenized Low-Density Lipoprotein-Induced ASMC Dysregulation Depends on circ_0000345-Mediated Regulatory Mechanism.

机构信息

Department of Cardiology, the Fourth Affiliated Hospital of Harbin Medical University.

出版信息

J Atheroscler Thromb. 2022 Dec 1;29(12):1849-1863. doi: 10.5551/jat.63327. Epub 2022 Sep 29.

Abstract

AIMS

Vascular smooth muscle cells are key participants in atherosclerosis. Circular RNA hsa_circ_0000345 (circ_0000345) and miR-647 are related to oxygenized low-density lipoprotein (ox-LDL)-induced arterial smooth muscle cell (ASMC) dysregulation. However, the relationship between circ_0000345 and miR-647 in ox-LDL-induced ASMC dysregulation is unclear.

METHODS

Relative levels of circ_0000345, miR-647, and PAP-associated domain containing 5 (PAPD5) mRNA in AS patient's serum and ox-LDL-induced ASMCs were detected via RT-qPCR. Gain-of-function experiments were utilized to analyze the effects of circ_0000345 upregulation on ox-LDL-induced cell proliferation, migration, invasion, and inflammatory response in ASMCs. The relationship between circ_0000345 or PAPD5 and miR-647 was validated by dual-luciferase reporter and RNA immunoprecipitation assays.

RESULTS

Circ_0000345 and PAPD5 were lowly expressed in AS patient's serum and ox-LDL-induced ASMCs, while miR-647 expression had an opposing trend. Mechanistically, circ_0000345 was verified as a miR-647 sponge, and miR-647 overexpression impaired the inhibitory effects of circ_0000345 upregulation on ox-LDL-induced ASMC proliferation, migration, invasion, and inflammatory response. Further experiments demonstrated that PAPD5 was a miR-647 target, and circ_0000345 adsorbed miR-647 to mediate PAPD5 expression. Also, PAPD5 inhibition relieved miR-647 silencing-mediated suppression on ox-LDL-induced ASMC proliferation, migration, invasion, and inflammatory response.

CONCLUSIONS

Circ_0000345 elevated PAPD5 expression via acting as a miR-647 sponge, resulting in alleviating ox-LDL-induced ASMC dysregulation. The study highlighted the critical role of circ_0000345 in AS.

摘要

目的

血管平滑肌细胞是动脉粥样硬化的关键参与者。环状 RNA hsa_circ_0000345(circ_0000345)和 miR-647 与氧化型低密度脂蛋白(ox-LDL)诱导的动脉平滑肌细胞(ASMC)失调有关。然而,circ_0000345 和 miR-647 在 ox-LDL 诱导的 ASMC 失调中的关系尚不清楚。

方法

通过 RT-qPCR 检测 AS 患者血清和 ox-LDL 诱导的 ASMC 中 circ_0000345、miR-647 和 PAP 相关结构域包含 5(PAPD5)mRNA 的相对水平。利用过表达实验分析 circ_0000345 上调对 ox-LDL 诱导的 ASMC 增殖、迁移、侵袭和炎症反应的影响。通过双荧光素酶报告和 RNA 免疫沉淀实验验证 circ_0000345 或 PAPD5 与 miR-647 的关系。

结果

circ_0000345 和 PAPD5 在 AS 患者血清和 ox-LDL 诱导的 ASMC 中表达水平较低,而 miR-647 的表达呈相反趋势。机制上,circ_0000345 被证实为 miR-647 的海绵体,miR-647 的过表达削弱了 circ_0000345 上调对 ox-LDL 诱导的 ASMC 增殖、迁移、侵袭和炎症反应的抑制作用。进一步的实验表明,PAPD5 是 miR-647 的靶基因,circ_0000345 通过吸附 miR-647 来调节 PAPD5 的表达。此外,PAPD5 抑制缓解了 miR-647 沉默对 ox-LDL 诱导的 ASMC 增殖、迁移、侵袭和炎症反应的抑制作用。

结论

circ_0000345 通过作为 miR-647 的海绵体来升高 PAPD5 的表达,从而减轻 ox-LDL 诱导的 ASMC 失调。该研究强调了 circ_0000345 在 AS 中的关键作用。

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