Induction of peripheral lymph node addressin in human nasal mucosa with eosinophilic chronic rhinosinusitis.

Abstract

Eosinophilic chronic rhinosinusitis (ECRS) is characterised by formation of nasal polyps with prominent eosinophilic infiltration; however, how eosinophils are recruited in this pathological setting remains unclear. In the present study, we carried out quantitative immunohistochemical analysis of nasal polyps associated with ECRS (n=30) and non-ECRS (n=30) to evaluate expression of an L-selectin ligand peripheral lymph node addressin (PNAd) on vascular endothelial cells. We found that PNAd was induced primarily on the luminal surface of venular vessels present in nasal mucosa in both ECRS and non-ECRS, while the number of PNAd-expressing vessels in ECRS significantly exceeded that seen in non-ECRS. Moreover, the number of eosinophils attached to the luminal surface of PNAd-expressing vessels in ECRS was significantly greater than that in non-ECRS, while the number of neutrophils and lymphocytes attached did not differ significantly between conditions. Furthermore, eosinophils, which express cell surface L-selectin, adhered to PNAd-expressing Chinese hamster ovary (CHO) cells in a calcium-dependent manner, and that adhesion was significantly inhibited by pretreatment of eosinophils with DREG-56, an anti-human L-selectin monoclonal antibody. These findings combined suggest that interaction between L-selectin and PNAd plays at least a partial role in eosinophil recruitment in human nasal mucosa with ECRS.

• Authors: Toshiki Tsutsumiuchi, Hitomi Hoshino, Shigeharu Fujieda, Motohiro Kobayashi
• Journal: Pathology (Pathology) Vol. 51 Issue 3 Pg. 268-273 (Apr 2019) ISSN: 1465-3931 [Electronic] England
• PMID: 30837082 (Publication Type: Journal Article)
• Copyright: Copyright © 2019 Royal College of Pathologists of Australasia. Published by Elsevier B.V. All rights reserved.

Chemical References

• Antigens, Surface
• L-selectin counter-receptors
• Membrane Proteins

Topics

• Animals
• Antigens, Surface (metabolism)
• CHO Cells
• Cricetinae
• Cricetulus
• Eosinophils (metabolism, pathology)
• Humans
• Membrane Proteins (metabolism)
• Nasal Mucosa (metabolism, pathology)
• Nasal Polyps (metabolism, pathology)
• Rhinitis (metabolism, pathology)
• Sinusitis (metabolism, pathology)