Exosomes mediate interepithelial transfer of functional P-glycoprotein in chronic rhinosinusitis with nasal polyps

Laryngoscope. 2017 Sep;127(9):E295-E300. doi: 10.1002/lary.26614. Epub 2017 May 9.

Abstract

Objective: P-glycoprotein (P-gp) drives type-2 helper T-cell inflammation in chronic rhinosinusitis with nasal polyps (CRSwNP) through unknown posttranslational mechanisms of overexpression. A recent randomized clinical trial demonstrated that inhibition of P-gp was as effective as oral steroids and biologics in treating CRSwNP. Exosomes are 30- to 150-nm vesicles capable of intercellular membrane protein transfer. The aims of this study were 1) to determine whether CRSwNP mucus exosomes are enriched with P-gp, and 2) whether exosomal P-gp can be functionally transferred to autologous epithelial cells as a putative mechanism for the proinflammatory overexpression of P-gp in CRSwNP.

Study design: Institutional review board-approved study in CRSwNP and control patients (n = 10 per group).

Methods: P-gp content of purified mucus exosomes was characterized by transmission electron microscopy and enzyme-linked immunosorbent assay. Epithelial transfer of exosomal P-gp was determined by time-lapse fluorescent microscopy and calcein acetoxymethylester functional P-gp assay.

Results: CD63+/P-gp+ exosomes were detected in both groups. P-gp was significantly enriched in CRSwNP exosomes relative to control (median 198.5; interquartile range 123.6-270.5 vs. 74.4; 41.3-95.0 pcg P-gp/109 exosomes, P = 0.002). Exosomes were absorbed by epithelial cells within 10 minutes, resulting in a significant increase in P-gp activity in CRSwNP patients relative to control (P = 0.006).

Conclusion: Here we demonstrate the presence and P-gp enrichment of mucus-derived exosomes, or rhinosomes, in CRSwNP. These rhinosomes are capable of rapid intercellular transfer of P-gp, leading to increased P-gp function within recipient cells. This represents a novel mechanism for maintaining P-gp overexpression in CRSwNP, and more generally for interepithelial transfer of other proteins between mucosal epithelial cells.

Level of evidence: NA. Laryngoscope, 127:E295-E300, 2017.

Keywords: Chronic rhinosinusitis with nasal polyps; P-glycoprotein; epithelium; exosome; rhinosome; sinonasal mucus.

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B, Member 1 / physiology*
  • Adult
  • Aged
  • Case-Control Studies
  • Cell Communication
  • Chronic Disease
  • Enzyme-Linked Immunosorbent Assay
  • Epithelial Cells / physiology
  • Exosomes / physiology*
  • Female
  • Humans
  • Male
  • Middle Aged
  • Nasal Mucosa / cytology
  • Nasal Polyps / metabolism*
  • Rhinitis / metabolism*
  • Sinusitis / metabolism*
  • Young Adult

Substances

  • ATP Binding Cassette Transporter, Subfamily B, Member 1