Proteomic analysis of pediatric sinonasal secretions shows increased MUC5B mucin in CRS

Amarel Saieg1, Kristy J Brown2, Maria T Pena3

  • 1Center for Genetic Medicine Research, Children's National Medical Center, Washington, DC.

Pediatric Research
|November 25, 2014
PubMed
Abstract

Insights

Pediatric chronic rhinosinusitis (CRS) involves increased MUC5B mucin in nasal secretions. This study identified MUC5B as significantly elevated in CRS patients compared to controls, validating proteomic findings.

Area of Science:

  • Otorhinolaryngology
  • Proteomics
  • Mucinology

Background:

  • Chronic rhinosinusitis (CRS) in children features excessive mucus and enlarged submucosal glands.
  • The protein composition of sinonasal secretions in pediatric CRS remains largely uncharacterized.
  • A hypothesis proposed a relative increase in glandular mucin MUC5B within CRS secretions.

Purpose of the Study:

  • To investigate the global protein profile of sinonasal secretions in pediatric CRS patients.
  • To determine the relative abundance of mucins, specifically MUC5B, in pediatric CRS.
  • To identify other proteins significantly altered in pediatric CRS sinonasal secretions.

Main Methods:

  • Sinonasal secretions were collected from pediatric CRS patients undergoing surgery and from control subjects.
  • Proteomic analysis involved protein extraction, tryptic digestion, and mass spectrometry.
  • Quantitative analysis utilized the QSpec algorithm for fold change significance, with Western blot validation.

Main Results:

  • A total of 294 proteins were identified in the sinonasal secretions.
  • MUC5B was found to be significantly more abundant in CRS samples compared to other mucins (P < 0.05).
  • Other significantly elevated proteins in CRS included BP1 fold-containing family A member 1, chitinase-3-like protein 1, plastin-2, serpin 10, and BP1 fold-containing family B member 1.

Conclusions:

  • The study confirms a significant increase in MUC5B abundance in the sinonasal secretions of pediatric CRS patients.
  • These findings highlight MUC5B as a potential biomarker in pediatric CRS.
  • The proteomic data provides insights into the molecular mechanisms underlying pediatric CRS.