Abstract

BackgroundThe involvement of secretoglobins (SCGBs) other than SCGB1A1 (Clara cell 10-kDa protein, CC10) in human airway diseases remains unexplored. Among those SCGBs, SCGB3A2 (uteroglobin-related protein 1, UGRP1) is particularly interesting, given its structure and function similarities with SCGB1A1 (CC10). The aim of this study was to investigate the expression regulation of SCGBs other than SCGB1A1 (CC10) in human upper airway, and their potential involvement, particularly that of SCGB3A2 (UGRP1), in chronic rhinosinusitis (CRS) with nasal polyps (CRSwNP) and without nasal polyps (CRSsNP).MethodsEight SCGB family members including SCGB3A2 (UGRP1), SCGB1C1 (ligand binding protein RYD5), SCGB1D1 (lipophilin A), SCGB1D2 (lipophilin B), SCGB1D4 (interferon-γ inducible SCGB), SCGB2A1 (mammaglobin 2), SCGB2A2 (mammaglobin 1), and SCGB3A1 (uteroglobin-related protein 2) were studied. The regulation of SCGBs mRNA expression in normal nasal mucosa by proinflammatory, Th1, and Th2 cytokines was studied through nasal explant culture. SCGBs mRNA expression levels in CRSsNP and CRSwNP patients and controls were compared. The mRNA levels were detected by means of quantitative reverse transcriptase-polymerase chain reaction. The protein expression of SCGB3A2 (UGRP1) was analyzed using immunohistochemistry.ResultsThe expression of SCGBs except SCGB1D2 (lipophilin B) could be found in upper airway and be differentially regulated by different cytokines. SCGB3A2 (UGRP1) mRNA expression was induced by Th1 cytokine, but suppressed by proinflammatory and Th2 cytokines. SCGBs mRNA expression was altered in CRS; particularly, SCGB3A2 (UGRP1) protein and mRNA expression was markedly decreased in both CRSsNP and CRSwNP and its protein levels inversely correlated with the number of total infiltrating cells, preoperative sinonasal CT scores, and postoperative endoscopy and symptom scores.ConclusionSCGBs except SCGB1D2 (lipophilin B) are expressed in human upper airway and their expression can be differentially regulated by inflammatory cytokines. SCGBs mRNA expression is altered in CRS. Reduced production of UGRP1, which is likely due, at least in part, to a local cytokine environment, may contribute to the hyper-inflammation in CRS and correlates with response to surgery.

Highlights

  • The involvement of secretoglobins (SCGBs) other than SCGB1A1 (Clara cell 10-kDa protein, CC10) in human airway diseases remains unexplored

  • Confirming the mRNA data, we found that SCGB3A2 (UGRP1) protein expression was significantly decreased in both CRSsNP and CRS with nasal polyps (CRSwNP) in comparison with controls and no significant difference was found between CRSsNP and CRSwNP (Figure 4B)

  • Analyzing the relationship between SCGB3A2 (UGRP1) staining intensity and the number of inflammatory cells, we found that SCGB3A2 (UGRP1) staining intensity inversely correlated with the number of total infiltrating cells (r = -0.485 and -0.558 in the CRSsNP and CRSwNP group, respectively; P < 0.05 for both), but did not correlate with the number of eosinophils or mononuclear cells

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Summary

Introduction

The involvement of secretoglobins (SCGBs) other than SCGB1A1 (Clara cell 10-kDa protein, CC10) in human airway diseases remains unexplored. Among those SCGBs, SCGB3A2 (uteroglobin-related protein 1, UGRP1) is interesting, given its structure and function similarities with SCGB1A1 (CC10). Nine members of this superfamily have been identified in humans, which includes SCGB1A1 (Clara cell 10-kDa protein, CC10), SCGB1C1 (ligand binding protein RYD5, RYD5), SCGB1D1 (lipophilin A, LIPA), SCGB1D2 (lipophilin B, LIPB), SCGB1D4 (interferon-g inducible SCGB, IIS), SCGB2A1 (mammaglobin 2, MGB2), SCGB2A2 (mammaglobin 1, MGB1), SCGB3A1 (uteroglobin-related protein 2, UGRP2), and SCGB3A2 (uteroglobin-related protein 1, UGRP1) [1,2,3,4,5]. As to other SCGBs, whether they are involved in airway diseases has been rarely studied

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