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Innate epithelial and functional differences in airway epithelium of children with acute wheeze
Journal article   Open access   Peer reviewed

Innate epithelial and functional differences in airway epithelium of children with acute wheeze

Kevin Looi, Thomas Iosifidis, Saraya Harrison, Stephen M. Stick, Peter LeSouef, Ingrid A. Laing and Anthony Kicic
Frontiers in cell and developmental biology, Vol.13, 1606915
2025
PMID: 40791985
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CC BY V4.0 Open Access

Abstract

Cell and Developmental Biology
Background: Early childhood wheeze is a major risk factor for asthma. However, not all children who wheeze will develop the disease. The airway epithelium has been shown to be involved in asthma pathogenesis. Despite this, the airway epithelium of children with acute wheeze remains poorly characterized. Methods: Upper airway epithelial cells (AEC) from children with acute wheeze and non-wheeze controls were cultured and expanded. Markers of epithelial lineage (Cytokeratin (KRT)-5, −19) and vimentin were assessed via qPCR and immunocytochemistry. Inflammatory cytokines (Interleukin (IL)-1β, −6, and −8) were measured using ELISA. Tight junction (TJ) protein expression and barrier integrity were determined via In-Cell Western and paracellular permeability assays, respectively. Results: Upper AECs from children with acute wheeze had significantly higher KRT19 and lower vimentin gene expression compared to non-wheeze controls but similar KRT5 levels. Similar staining intensities of KRT5 and KRT19 proteins were observed in both cohorts. IL-6 and IL-8 levels were not significantly different, but IL-1β was increased in cultures from children with acute wheeze compared to controls. Tight junction protein expression of claudin-1, occludin and ZO-1 were significantly lower in acute wheeze cohorts, concomitant with increased paracellular permeability. Conclusion: Airway epithelium of children experiencing acute wheeze appears abnormal, primarily with compromised epithelial barrier integrity.

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Collaboration types
Domestic collaboration
Citation topics
1 Clinical & Life Sciences
1.65 Allergy
1.65.44 Asthma
Web Of Science research areas
Cell Biology
Developmental Biology
ESI research areas
Molecular Biology & Genetics
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