Academy of Medical Sciences & Department of Immunology, College of Basic Medical Sciences, Zhengzhou University, Zhengzhou, Henan, 450052, China.
Priority Research Centre for Healthy Lungs, School of Biomedical Sciences & Pharmacy, College of Health, Medicine and Wellbeing and Hunter Medical Research Institute, University of Newcastle, Callaghan, NSW, 2300, Australia.
Mucosal Immunol. 2022 Jun;15(6):1363-1374. doi: 10.1038/s41385-022-00556-1. Epub 2022 Aug 29.
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.
导致哮喘恶化的免疫反应与过敏原或病毒暴露有关。确定常见的免疫因素将有利于制定统一的靶向治疗方法。我们采用屋尘螨(HDM)哮喘小鼠模型,用过敏原(HDM、蟑螂提取物(CRE))或呼吸道合胞病毒(RSV)对过敏性 HDM 小鼠进行挑战。纯化的肺免疫细胞进行高维单细胞 RNA 深度测序(scRNA-seq),以生成 RNA 转录组。用 siRNA 进行基因沉默以确认 scRNA-seq 分析的有效性。scRNA-seq UMAP 分析描绘了单个免疫簇内的一系列细胞标记。SCENIC R 分析显示 CD11b DC 细胞中的调控子数量和活性增加。保守调控子因子的分析进一步确定 Creb5 是恶化组之间的共享调控子。Creb5 siRNA 减弱了 HDM、CRE 或 RSV 诱导的哮喘恶化。免疫簇的 scRNA-seq 多维分析确定了恶化组之间保守的基因途径。我们提出,这些分析为识别多方面病理中的特定治疗靶点提供了一个强有力的框架。