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.