posted on 2025-05-10, 19:57authored byXiaojie Liu, Keilah G. Netto, Paul S. Foster, Fuguang Li, Ming YangMing Yang, Leon A. Sokulsky, Lujia Zhou, Huisha Xu, Chi Liu, Ming Wang, Huaqi Wang, Hui Li, Guojun Zhang
Immune responses that result in asthma exacerbation are associated with allergen or viral exposure. Identification of common immune factors will be beneficial for the development of uniformed targeted therapy. We employed a House Dust Mite (HDM) mouse model of asthma and challenged allergic HDM mice with allergens (HDM, cockroach extract (CRE)) or respiratory syncytial virus (RSV). Purified lung immune cells underwent high-dimensional single-cell RNA deep sequencing (scRNA-seq) to generate an RNA transcriptome. Gene silencing with siRNA was employed to confirm the efficacy of scRNA-seq analysis. scRNA-seq UMAP analysis portrayed an array of cell markers within individual immune clusters. SCENIC R analysis showed an increase in regulon number and activity in CD11b- DC cells. Analysis of conserved regulon factors further identified Creb5 as a shared regulon between the exacerbation groups. Creb5 siRNAs attenuated HDM, CRE or RSV-induced asthma exacerbation. scRNA-seq multidimensional analysis of immune clusters identified gene pathways that were conserved between the exacerbation groups. We propose that these analyses provide a strong framework that could be used to identify specific therapeutic targets in multifaceted pathologies.
History
Journal title
Mucosal Immunology
Volume
15
Issue
6
Pagination
1363-1374
Publisher
Elsevier
Language
en, English
College/Research Centre
College of Health, Medicine and Wellbeing
School
School of Biomedical Sciences and Pharmacy
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