Zonula occludens-1 expression is reduced in nasal epithelial cells of allergic rhinitis patients

PeerJ. 2022 Apr 22:10:e13314. doi: 10.7717/peerj.13314. eCollection 2022.

Abstract

Allergic rhinitis (AR) is a common allergic disease characterized by disruption of nasal epithelial barrier. In this study, we investigated the mRNA expression of zonula occludens-1 (ZO-1), ZO-2 and ZO-3 and histone deacetylase 1 (HDAC1) and HDAC2 in AR patients compared to healthy controls. RNA samples were extracted from nasal epithelial cells of house dust mites (HDMs)-sensitized AR patients and healthy controls (n = 28 in each group). The RNAs were reverse transcribed into cDNAs for measurement of ZO-1, ZO-2, ZO-3, HDAC1 and HDAC2 expression levels by quantitative PCR. The mRNA expression of ZO-1 was significantly decreased in AR patients compared to healthy controls (p = 0.010). No significant difference was observed in the expression levels of ZO-2, ZO-3, HDAC1 and HDAC2 in AR patients compared to healthy controls. We found significant associations of higher HDAC2 levels in AR patients with lower frequency of changing bedsheet (p = 0.043) and with AR patients sensitized to Dermatophagoides farinae (p = 0.041). Higher expression of ZO-2 was observed in AR patients who had pets (p = 0.007). In conclusion, our data indicated that ZO-1 expression was lower in AR patients contributing to decreased integrity of nasal epithelial barrier integrity, and HDAC2 may be involved in the pathogenesis of the disease.

Keywords: Allergic rhinitis; HDAC1; HDAC2; Histone deacetylase; House dust mites; ZO-1; ZO-2; ZO-3; Zonula occludens.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Epithelial Cells / metabolism
  • Humans
  • Nasal Mucosa / metabolism
  • RNA, Messenger / metabolism
  • Rhinitis, Allergic* / metabolism
  • Tight Junctions / metabolism
  • Zonula Occludens-1 Protein* / genetics
  • Zonula Occludens-1 Protein* / metabolism

Substances

  • RNA, Messenger
  • TJP1 protein, human
  • Zonula Occludens-1 Protein

Grants and funding

This work was supported by the research grant from Universiti Sains Malaysia (USM) comprised of a Research University Grant (1001.PPSP.8012285) awarded to Noor Suryani Mohd Ashari and a Research University Grant (1001.PPSP.8012349) awarded to Kah Keng Wong. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.