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Analysis of Combinatorial miRNA Treatments to Regulate Cell Cycle and Angiogenesis
Published on: March 30, 2019
Hsa_circ_0008360 sponges miR-186-5p to target CCND2 to modulate high glucose-induced vascular endothelial dysfunction
Qian-Qian Zhu1, Xi-Bin Pu1, Tian-Chi Chen1
1Department of Vascular Surgery, the First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, Zhejiang Province, P.R. China.
Insights
Circular RNA hsa_circ_0008360 exacerbates high glucose-induced vascular endothelial dysfunction by sponging miR-186-5p and targeting CCND2. Silencing circ_0008360 protects against endothelial dysfunction, suggesting it as a therapeutic target.
Area of Science:
- Molecular Biology
- Cell Biology
- Biochemistry
Background:
- Vascular endothelial dysfunction is a critical factor in disease progression.
- Circular RNAs (circRNAs) are implicated in vascular endothelial dysfunction.
- The specific role of circRNA hsa_circ_0008360 (circ_0008360) in high glucose-induced endothelial dysfunction is not well understood.
Purpose of the Study:
- To investigate the role and mechanism of circ_0008360 in high glucose-induced human umbilical vascular endothelium cell (HUVEC) dysfunction.
- To explore the regulatory pathway involving circ_0008360, miR-186-5p, and cyclin D2 (CCND2).
Main Methods:
- Human umbilical vascular endothelium cells (HUVECs) were treated with high glucose (HG).
- Quantitative real-time polymerase chain reaction (qRT-PCR) and western blot were used to measure circ_0008360, miR-186-5p, and CCND2 levels.
- Cell viability, apoptosis, migration, and tube formation assays assessed endothelial dysfunction.
- Dual-luciferase reporter, RNA pull-down, and RNA immunoprecipitation (RIP) assays determined molecular interactions.
Main Results:
- Circ_0008360 expression was significantly upregulated in HG-treated HUVECs.
- Knockdown of circ_0008360 improved cell viability, migration, and tube formation, while reducing apoptosis in HG conditions.
- Circ_0008360 acted as a molecular sponge for miR-186-5p; miR-186-5p targeted CCND2, and this pathway mediated the protective effects of circ_0008360 silence.
Conclusions:
- Circ_0008360 knockdown attenuates high glucose-induced vascular endothelial dysfunction by regulating the miR-186-5p/CCND2 axis.
- Circ_0008360 may serve as a potential therapeutic target for treating vascular endothelial dysfunction.
Abstract:
Vascular endothelial dysfunction is associated with the progress of many diseases. Circular RNAs (circRNAs) take part in the dysfunction of vascular endothelium. CircRNA hsa_circ_0008360 (circ_0008360) is dysregulated in high glucose-treated vascular endothelium, while the role and mechanism of circ_0008360 in high glucose-induced dysfunction remain unknown. Human umbilical vascular endothelium cells (HUVEC) were stimulated via high glucose. The abundances of circ_0008360, miR-186-5p and cyclin D2 (CCND2) were examined via quantitative real-time polymerase chain reaction or western blot. Vascular endothelial dysfunction was assessed via cell viability, apoptosis, migration and tube formation. The target relationship between miR-186-5p and circ_0008360 or CCND2 was analyzed via dual-luciferase reporter, RNA pull-down and RNA immunoprecipitation analyses. Circ_0008360 expression was enhanced in high-glucose-treated HUVEC. Circ_0008360 silence mitigated high glucose-induced suppression of viability, migration, tube formation, and increase in apoptosis in HUVEC. MiR-186-5p was sponged by circ_0008360, and miR-186-5p inhibition reversed the effect of circ_0008360 silence on high glucose-induced vascular endothelial dysfunction. MiR-186-5p alleviated high glucose-induced vascular endothelial dysfunction via targeting CCND2. CCND2 interference abolished the aggravated effect of circ_0008360 on high glucose-induced vascular endothelial dysfunction. Circ_0008360 knockdown attenuated high glucose-induced vascular endothelial dysfunction via regulating miR-186-5p and CCND2, indicating circ_0008360 might act as a target for the treatment of vascular endothelial dysfunction.Abbreviations: circRNAs, circular RNAs; HUVEC, human umbilical vascular endothelium cells; CCND2, cyclin D2; XPNPEP3, X-prolyl aminopeptidase 3; ceRNAs, competing endogenous RNAs; miRNAs, microRNAs; qRT-PCR, quantitative real-time polymerase chain reaction; RIP, RNA immunoprecipitation; HIF-1α, hypoxia inducible factor 1 alpha; TLR3, toll-like receptor 3; AKAP12, A-Kinase Anchoring Protein 12; ox-LDL, oxidized low-density lipoprotein; HG, high glucose; NG, normal glucose.
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