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环状 RNA circPHKA2 通过竞争性结合 miR-574-5p 调控 SOD2 缓解 OGD 诱导的人脑微血管内皮细胞损伤

Circular RNA circPHKA2 Relieves OGD-Induced Human Brain Microvascular Endothelial Cell Injuries through Competitively Binding miR-574-5p to Modulate SOD2.

机构信息

Department of Neurosurgery, The Affiliated Hospital of Southwest Medical University, China.

Sichuan Clinical Research Center for Neurosurgery, China.

出版信息

Oxid Med Cell Longev. 2021 Nov 8;2021:3823122. doi: 10.1155/2021/3823122. eCollection 2021.

Abstract

BACKGROUND

Circular RNA phosphorylase kinase regulatory subunit alpha 2 (circPHKA2; hsa_circ_0090002) has a significantly, specifically different expression in acute ischemic stroke (AIS) patients' blood. Here, we intended to investigate the role and mechanism of circPHKA2 in oxygen-glucose deprivation- (OGD-) induced stoke model in human brain microvascular endothelial cells (HBMEC).

METHODS

Expression of circPHKA2, microRNA- (miR-) 574-5p, and superoxide dismutase-2 (SOD2) was detected by quantitative PCR and western blotting. Cell injury was measured by detecting cell proliferation (EdU assay and CCK-8 assay), migration (transwell assay), neovascularization (tube formation assay), apoptosis (flow cytometry and western blotting), endoplasmic reticulum stress (western blotting), and oxidative stress (assay kits). Direct intermolecular interaction was determined by bioinformatics algorithms, dual-luciferase reporter assay, biotin-labelled miRNA capture, and argonaute 2 RNA immunoprecipitation.

RESULTS

circPHKA2 was downregulated in AIS patients' blood in SOD2-correlated manner. Reexpressing circPHKA2 rescued EdU incorporation, cell viability and migration, tube formation, B cell lymphoma-2 (Bcl-2) expression, and SOD activity of OGD-induced HBMEC and alleviate apoptotic rate and levels of Bcl-2-associated protein (Bax), glucose-regulated protein 78 kD (GRP78), C/EBP-homologous protein (CHOP), caspase-12, reactive oxygen species (ROS), and malondialdehyde (MDA). Additionally, blocking SOD2 partially attenuated these roles of circPHKA2 overexpression. Molecularly, circPHKA2 upregulated SOD2 expression via interacting with miR-574-5p, and miR-574-5p could target SOD2. Similarly, allied to neurovascular protection of circPHKA2 was the downregulation of miR-574-5p.

CONCLUSION

circPHKA2 could protect HBMEC against OGD-induced cerebral stroke model via the miR-574-5p/SOD2 axis, suggesting circPHKA2 as a novel and promising candidate in ischemic brain injury.

摘要

背景

环状 RNA 磷酸化酶激酶调节亚基α 2(circPHKA2;hsa_circ_0090002)在急性缺血性脑卒中(AIS)患者的血液中有明显的、特异性的差异表达。在这里,我们旨在研究 circPHKA2 在人脑血管内皮细胞(HBMEC)氧葡萄糖剥夺(OGD)诱导的中风模型中的作用和机制。

方法

通过定量 PCR 和 Western blot 检测 circPHKA2、microRNA-(miR-)574-5p 和超氧化物歧化酶-2(SOD2)的表达。通过检测细胞增殖(EdU 检测和 CCK-8 检测)、迁移(Transwell 检测)、新生血管形成(管形成检测)、细胞凋亡(流式细胞术和 Western blot)、内质网应激(Western blot)和氧化应激(试剂盒)来测量细胞损伤。通过生物信息学算法、双荧光素酶报告基因检测、生物素标记的 miRNA 捕获和 Argonaute 2 RNA 免疫沉淀来确定直接分子间相互作用。

结果

circPHKA2在 SOD2 相关的方式下调 AIS 患者的血液中。在 OGD 诱导的 HBMEC 中,再表达 circPHKA2 可恢复 EdU 掺入、细胞活力和迁移、管形成、B 细胞淋巴瘤-2(Bcl-2)表达和 SOD 活性,并减轻凋亡率和 Bcl-2 相关蛋白(Bax)、葡萄糖调节蛋白 78kD(GRP78)、C/EBP 同源蛋白(CHOP)、半胱天冬酶-12、活性氧(ROS)和丙二醛(MDA)的水平。此外,阻断 SOD2 可部分减弱 circPHKA2 过表达的这些作用。分子上,circPHKA2 通过与 miR-574-5p 相互作用而上调 SOD2 的表达,并且 miR-574-5p 可以靶向 SOD2。同样,circPHKA2 对神经血管的保护作用与 miR-574-5p 的下调有关。

结论

circPHKA2 通过 miR-574-5p/SOD2 轴保护 HBMEC 免受 OGD 诱导的脑中风模型,表明 circPHKA2 作为缺血性脑损伤的一种新的有前途的候选物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc17/8592726/0eb8276843f8/OMCL2021-3823122.001.jpg

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