The EphA1 and EphA2 Signaling Modulates the Epithelial Permeability in Human Sinonasal Epithelial Cells and the Rhinovirus Infection Induces Epithelial Barrier Dysfunction via EphA2 Receptor Signaling

Int J Mol Sci. 2023 Feb 11;24(4):3629. doi: 10.3390/ijms24043629.

Abstract

Deficiencies in epithelial barrier integrity are involved in the pathogenesis of chronic rhinosinusitis (CRS). This study aimed to investigate the role of ephrinA1/ephA2 signaling on sinonasal epithelial permeability and rhinovirus-induced epithelial permeability. This role in the process of epithelial permeability was evaluated by stimulating ephA2 with ephrinA1 and inactivating ephA2 with ephA2 siRNA or inhibitor in cells exposed to rhinovirus infection. EphrinA1 treatment increased epithelial permeability, which was associated with decreased expression of ZO-1, ZO-2, and occludin. These effects of ephrinA1 were attenuated by blocking the action of ephA2 with ephA2 siRNA or inhibitor. Furthermore, rhinovirus infection upregulated the expression levels of ephrinA1 and ephA2, increasing epithelial permeability, which was suppressed in ephA2-deficient cells. These results suggest a novel role of ephrinA1/ephA2 signaling in epithelial barrier integrity in the sinonasal epithelium, suggesting their participation in rhinovirus-induced epithelial dysfunction.

Keywords: chronic rhinosinusitis; ephrinA1; ephrinA2 receptor; epithelial barrier; rhinovirus.

MeSH terms

  • Cell Membrane Permeability* / genetics
  • Cell Membrane Permeability* / physiology
  • Epithelial Cells* / metabolism
  • Epithelial Cells* / physiology
  • Humans
  • Picornaviridae Infections / metabolism
  • RNA, Double-Stranded
  • RNA, Small Interfering / metabolism
  • Receptor, EphA1*
  • Receptor, EphA2* / metabolism
  • Rhinovirus / pathogenicity
  • Signal Transduction / physiology

Substances

  • Receptor, EphA1
  • Receptor, EphA2
  • RNA, Double-Stranded
  • RNA, Small Interfering

Grants and funding

This work was supported by The Basic Science Research Program through the National Research Foundation of Korea (2022R1A2C1003461).