Differential Expression of the Aryl Hydrocarbon Receptor and Transforming Growth Factor Beta 1 in Chronic Rhinosinusitis with Nasal Polyps with Allergic Rhinitis

ORL J Otorhinolaryngol Relat Spec. 2017;79(6):295-305. doi: 10.1159/000481510. Epub 2017 Nov 29.

Abstract

Objective: This study aimed to determine the aryl hydrocarbon receptor (AhR) and transforming growth factor beta 1 (TGF-β1) expression levels in chronic rhinosinusitis (CRS) and their possible correlation with allergic state and tissue remodeling.

Methods: Patients were enrolled and divided into the following groups: CRS without nasal polyps (NP) without allergic rhinitis (AR) (CRSsNPsAR; n = 20), CRS with NP with AR (CRSwNPwAR; n = 20), CRS with NP without AR (CRSwNPsAR; n = 20), and controls (n = 15). Tissue samples were analyzed by Masson trichrome staining for collagen, while the location and expression of AhR and TGF-β1 were analyzed by immunohistochemistry, quantitative reverse transcription polymerase chain reaction (qRT-PCR), and Western blotting.

Results: The collagen amounts as well as AhR and TGF-β1 mRNA and protein expression levels were significantly increased in the CRSsNPsAR group compared with the CRSwNP (CRSwNPsAR and CRSwNPwAR) samples (p < 0.01). However, higher collagen amounts (p < 0.05) and higher TGF-β1 (p < 0.05) but lower AhR expression levels (p < 0.05) were detected in the CRSwNPwAR versus the CRSwNPsAR patients. Both AhR and TGF-β1 expression were positively correlated with the collagen level in CRS samples (p < 0.01).

Conclusions: Elevated AhR expression may be involved in the progression of tissue remodeling in CRSsNPsAR similar to TGF-β1 expression. Conversely, lower AhR expression may be involved in allergic reactions in CRSwNPwAR.

Keywords: Allergic rhinitis; Aryl hydrocarbon receptor; Chronic rhinosinusitis; Nasal polyps; Transforming growth factor beta 1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Blotting, Western
  • Chronic Disease
  • Collagen / metabolism
  • Female
  • Genetic Predisposition to Disease
  • Humans
  • Immunohistochemistry
  • Male
  • Middle Aged
  • Nasal Mucosa / metabolism
  • Nasal Mucosa / pathology
  • Nasal Polyps / complications
  • Nasal Polyps / metabolism*
  • Paranasal Sinuses / metabolism
  • Paranasal Sinuses / pathology
  • Real-Time Polymerase Chain Reaction
  • Receptors, Aryl Hydrocarbon / metabolism*
  • Rhinitis / complications
  • Rhinitis / metabolism*
  • Sinusitis / complications
  • Sinusitis / metabolism*
  • Transforming Growth Factor beta1 / metabolism*
  • Young Adult

Substances

  • Receptors, Aryl Hydrocarbon
  • Transforming Growth Factor beta1
  • Collagen