Aryl hydrocarbon receptor and IL-13 signaling crosstalk in human keratinocytes and atopic dermatitis

Atopic dermatitis (AD) is an allergic skin disease mediated by skin barrier impairment and IL-13-driven immune response. Activation of the aryl hydrocarbon receptor (AHR) has shown promise in early clinical trials for AD; however, the mechanism by which AHR partially ameliorates AD is not well known...

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Veröffentlicht in:Frontiers in allergy 2024, Vol.5, p.1323405-1323405
Hauptverfasser: Proper, Steven P, Dwyer, Alexander T, Appiagyei, Andrews, Felton, Jennifer M, Ben-Baruch Morgenstern, Netali, Marlman, Justin M, Kotliar, Michael, Barski, Artem, Troutman, Ty D, Rothenberg, Marc E, Mersha, Tesfaye B, Azouz, Nurit P
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Sprache:eng
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Zusammenfassung:Atopic dermatitis (AD) is an allergic skin disease mediated by skin barrier impairment and IL-13-driven immune response. Activation of the aryl hydrocarbon receptor (AHR) has shown promise in early clinical trials for AD; however, the mechanism by which AHR partially ameliorates AD is not well known. Gene expression data from human biopsies were analyzed, and compared to gene expression from RNA-sequencing in our HaCaT cell model system. Western blot, ELISA qRT-PCR were used to further explore the relationship between AHR and IL-13 signaling in HaCaT cells. The AHR target gene decreased in lesional skin compared with healthy control skin (  = 4.30 × 10 ). Single-cell RNA sequencing (scRNAseq) demonstrated increased expression (  
ISSN:2673-6101
2673-6101
DOI:10.3389/falgy.2024.1323405