Inhibition of hsa_circ_0002570 suppresses high-glucose-induced angiogenesis and inflammation in retinal microvascular endothelial cells through miR-1243/angiomotin axis

Cell Stress Chaperones. 2020 Sep;25(5):767-777. doi: 10.1007/s12192-020-01111-2. Epub 2020 Apr 21.

Abstract

Diabetic retinopathy (DR) is the most severe microvascular complication of diabetes and a major cause of visual impairment and blindness. However, the treatment for DR is still limited. Our study aimed to explore the role of circular RNA_0002570 in DR. First, we predicted the potential microRNA and mRNA that could bind to circ_0002570 and identified the miR-1243 and angiomotin gene; then, we used RT-PCR and Western blot to measure their expression. Next, we evaluated the abilities of proliferation, migration, and angiogenesis in vitro in human retinal microvascular endothelial cells (hRMECs) by CCK-8, transwell assay, and tube formation assay, respectively. To analyze the relationship among miR-1243, circ_0002570, and angiomotin, RNA pull-down and luciferase assay were performed. Our results showed that, in DR patients and high-glucose-induced hRMECs, miR-1243, circ_0002570, and angiomotin were all abnormally expressed. MiR-1243 could directly and competitively bind to both circ_0002570 and angiomotin mRNA to inhibit their expression. Moreover, circ_0002570 suppressed the abilities of proliferation, migration, and angiogenesis in hRMECs induced by high glucose, which was dependent on miR-1243-angiomotin axis. Furthermore, circ_0002570 could upregulate angiomotin by targeting miR-1243 to mediate the dysfunction of hRMECs induced by high glucose. In conclusion, circ_0002570 might serve as a potential target for diagnosis and treatment for DR.

Keywords: Angiomotin; Diabetic retinopathy; ceRNA; hsa-circ-0002570; miR1243.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Angiomotins
  • Cell Line
  • Diabetic Retinopathy / metabolism*
  • Diabetic Retinopathy / pathology
  • Endothelial Cells / cytology
  • Endothelial Cells / metabolism*
  • Humans
  • Intercellular Signaling Peptides and Proteins / metabolism*
  • MicroRNAs / metabolism*
  • Microfilament Proteins / metabolism*
  • Neovascularization, Pathologic
  • RNA, Circular / metabolism*

Substances

  • AMOT protein, human
  • Angiomotins
  • Intercellular Signaling Peptides and Proteins
  • MIRN1243 microRNA, human
  • MicroRNAs
  • Microfilament Proteins
  • RNA, Circular