Circular RNA circ_0001445 alleviates the ox-LDL-induced endothelial injury in human primary aortic endothelial cells through regulating ABCG1 via acting as a sponge of miR-208b-5p
- PMID: 35391605
- DOI: 10.1007/s11748-022-01799-2
Circular RNA circ_0001445 alleviates the ox-LDL-induced endothelial injury in human primary aortic endothelial cells through regulating ABCG1 via acting as a sponge of miR-208b-5p
Abstract
Background: Coronary artery disease (CAD) originates from the blockage of the inner walls of the coronary arteries due to a plaque buildup. Circular RNA (circRNA) circ_0001445 has been reported to be downregulated in patients with a higher coronary atherosclerotic burden. This study is designed to explore the role and mechanism of circ_0001445 on the oxidized low-density lipoprotein (ox-LDL)-induced endothelial cell damage.
Methods: Circ_0001445, microRNA-208b-5p (miR-208b-5p), and ATP-binding cassette sub-family G member 1 (ABCG1) levels were detected by real-time quantitative polymerase chain reaction (RT-qPCR). Inflammatory cytokines levels, cell viability, proliferation, migration were detected by Enzyme-linked immunosorbent assay (ELISA) kits, Cell Counting Kit-8 (CCK-8), 5-ethynyl-2'-deoxyuridine (EdU), and transwell assays, respectively. Protein levels were determined by western blot assay. The binding between miR-208b-5p and circ_0001445 or ABCG1 was predicted by circBank or TargetScan, and then verified by a dual-luciferase reporter, RNA Immunoprecipitation (RIP), and RNA pull-down assays.
Results: Circ_0001445 and ABCG1 were decreased, and miR-208b-5p was increased in CAD patients and ox-LDL-treated HAECs. Also, circ_0001445 overexpression could weaken ox-LDL-triggered HAEC injury by boosting proliferation, migration, and repressing inflammation and extracellular matrix (ECM). Mechanically, circ_0001445 directly targeted miR-208b-5p. Furthermore, miR-208b-5p mediated the modulation of circ_0001445 in ox-LDL-induced HAEC injury. ABCG1 acted as a direct target of miR-208b-5p, and the downregulation of miR-208b-5p relieved ox-LDL-induced HAEC damage by interacting with ABCG1. Additionally, circ_0001445 regulated ABCG1 expression by sponging miR-208b-5p.
Conclusion: Circ_0001445 could abate ox-LDL-mediated HAEC damage by the miR-208b-5p/ABCG1 axis, providing a novel insight into the pathogenesis and treatment of CAD.
Keywords: ABCG1; Circ_0001445; Coronary artery disease; Mir-208b-5p; Ox-LDL.
© 2022. The Author(s), under exclusive licence to The Japanese Association for Thoracic Surgery.
Similar articles
-
Role and mechanism of circular RNA circ_0050486 in regulating oxidized low-density lipoprotein-induced injury in endothelial cells.Clin Hemorheol Microcirc. 2022;82(2):107-124. doi: 10.3233/CH-211259. Clin Hemorheol Microcirc. 2022. PMID: 35723090
-
Circular RNA circ_0124644 exacerbates the ox-LDL-induced endothelial injury in human vascular endothelial cells through regulating PAPP-A by acting as a sponge of miR-149-5p.Mol Cell Biochem. 2020 Aug;471(1-2):51-61. doi: 10.1007/s11010-020-03764-0. Epub 2020 Jun 4. Mol Cell Biochem. 2020. PMID: 32500475
-
Circ_0093887 upregulates CCND2 and SUCNR1 to inhibit the ox-LDL-induced endothelial dysfunction in atherosclerosis by functioning as a miR-876-3p sponge.Clin Exp Pharmacol Physiol. 2021 Aug;48(8):1137-1149. doi: 10.1111/1440-1681.13504. Epub 2021 Apr 29. Clin Exp Pharmacol Physiol. 2021. PMID: 33844344
-
Silencing of OIP5-AS1 Protects Endothelial Cells From ox-LDL-Triggered Injury by Regulating KLF5 Expression via Sponging miR-135a-5p.Front Cardiovasc Med. 2021 Mar 12;8:596506. doi: 10.3389/fcvm.2021.596506. eCollection 2021. Front Cardiovasc Med. 2021. PMID: 33778018 Free PMC article.
-
CircUsp9x/miR-599/stim1 axis regulates proliferation and migration in vascular smooth muscle cells induced by oxidized-low density lipoprotein.Clin Exp Hypertens. 2023 Dec 31;45(1):2280758. doi: 10.1080/10641963.2023.2280758. Epub 2023 Nov 14. Clin Exp Hypertens. 2023. PMID: 37963203 Review.
Cited by
-
The potential role and mechanism of circRNAs in foam cell formation.Noncoding RNA Res. 2023 Mar 21;8(3):315-325. doi: 10.1016/j.ncrna.2023.03.005. eCollection 2023 Sep. Noncoding RNA Res. 2023. PMID: 37032721 Free PMC article. Review.
-
CircRNA Networks in CAD: Multi-Cellular Mechanisms and Clinical Potential.Int J Gen Med. 2025 Jun 12;18:3129-3150. doi: 10.2147/IJGM.S524189. eCollection 2025. Int J Gen Med. 2025. PMID: 40529348 Free PMC article. Review.
-
Extracellular Non-Coding RNAs in Cardiovascular Diseases.Pharmaceutics. 2023 Jan 3;15(1):155. doi: 10.3390/pharmaceutics15010155. Pharmaceutics. 2023. PMID: 36678784 Free PMC article. Review.
-
Genetic and Epigenetic Regulation of Lipoxygenase Pathways and Reverse Cholesterol Transport in Atherogenesis.Genes (Basel). 2022 Aug 18;13(8):1474. doi: 10.3390/genes13081474. Genes (Basel). 2022. PMID: 36011386 Free PMC article. Review.
-
Role of Circular RNAs in Atherosclerosis through Regulation of Inflammation, Cell Proliferation, Migration, and Apoptosis: Focus on Atherosclerotic Cerebrovascular Disease.Medicina (Kaunas). 2023 Aug 14;59(8):1461. doi: 10.3390/medicina59081461. Medicina (Kaunas). 2023. PMID: 37629751 Free PMC article. Review.
References
-
- Malakar AK, Choudhury D, Halder B, et al. A review on coronary artery disease, its risk factors, and therapeutics. J Cell Physiol. 2019;234(10):16812–23. https://doi.org/10.1002/jcp.28350 . - DOI - PubMed
-
- McCullough PA. Coronary artery disease. Clin J Am Soc Nephrol. 2007;2(3):611–6. https://doi.org/10.2215/cjn.03871106 . - DOI - PubMed
-
- Li X, Wu C, Lu J, et al. Cardiovascular risk factors in China: a nationwide population-based cohort study. Lancet Public Health. 2020;5(12):e672–81. https://doi.org/10.1016/s2468-2667(20)30191-2 . - DOI - PubMed
-
- Liu L. Cardiovascular diseases in China. Biochem Cell Biol. 2007;85(2):157–63. https://doi.org/10.1139/o07-004 . - DOI - PubMed
-
- Bentzon JF, Otsuka F, Virmani R, et al. Mechanisms of plaque formation and rupture. Circ Res. 2014;114(12):1852–66. https://doi.org/10.1161/circresaha.114.302721 . - DOI - PubMed
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Miscellaneous