Specific Circular RNA Signature of Endothelial Cells: Potential Implications in Vascular Pathophysiology

Leïla Halidou Diallo1, Jérôme Mariette2, Nathalie Laugero1

  • 1U1297-I2MC, INSERM, University of Toulouse, 1 Avenue Jean Poulhes, BP 84225, 31432 Toulouse, France.

Insights

Circular RNAs (circRNAs) show cell-specific expression in endothelial cells, offering unique signatures for cell identification. Four specific circRNAs (circCARD6, circPLXNA2, circCASC15, circEPHB4) are linked to vascular functions and cancer.

Area of Science:

  • Vascular Biology
  • Genomics
  • Cancer Research

Background:

  • Circular RNAs (circRNAs) are emerging regulators of gene expression.
  • Previous studies linked circRNAs to endothelial and cancer cell functions independently.
  • No comparative analysis of circRNA expression across different endothelial cell types existed.

Purpose of the Study:

  • To comparatively analyze circRNA expression profiles in arterial, venous, and lymphatic endothelial cells.
  • To identify common and distinct circRNA signatures.
  • To explore the potential of circRNAs in understanding vascular physiology and pathology.

Main Methods:

  • Analysis of public and original RNA sequencing datasets.
  • Identification and comparison of circRNA expression across endothelial cell types.
  • Bioinformatic analysis to determine circRNA origin and cell-specific signatures.

Main Results:

  • Identified 4713 distinct circRNAs, with 95% originating from exons.
  • Demonstrated that circRNA expression is more cell-type specific than linear RNA.
  • Discovered unique circRNA signatures for each endothelial cell type.
  • Identified a four-circRNA signature (circCARD6, circPLXNA2, circCASC15, circEPHB4) specific to endothelial cells.

Conclusions:

  • CircRNA expression profiles are highly specific to endothelial cell types, outperforming linear RNAs for cell discrimination.
  • A novel endothelial cell-specific circRNA signature was identified, implicating genes in migration and cancer progression.
  • These findings may enhance understanding of (lymph)angiogenesis and tumor metastasis, offering new therapeutic targets.