Single-cell transcriptomic characterization reveals the landscape of airway remodeling and inflammation in a cynomolgus monkey model of asthma.

IF 8.3 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY
ACS Applied Materials & Interfaces Pub Date : 2022-11-10 eCollection Date: 2022-01-01 DOI:10.3389/fimmu.2022.1040442
Yingshuo Wang, Xinyan Dong, Caizhe Pan, Cihang Zhu, Hantao Qi, Yifan Wang, Hao Wei, Qiangmin Xie, Lei Wu, Huijuan Shen, Shuxian Li, Yicheng Xie
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Abstract

Monkey disease models, which are comparable to humans in terms of genetic, anatomical, and physiological characteristics, are important for understanding disease mechanisms and evaluating the efficiency of biological treatments. Here, we established an A.suum-induced model of asthma in cynomolgus monkeys to profile airway inflammation and remodeling in the lungs by single-cell RNA sequencing (scRNA-seq). The asthma model results in airway hyperresponsiveness and remodeling, demonstrated by pulmonary function test and histological characterization. scRNA-seq reveals that the model elevates the numbers of stromal, epithelial and mesenchymal cells (MCs). Particularly, the model increases the numbers of endothelial cells (ECs), fibroblasts (Fibs) and smooth muscle cells (SMCs) in the lungs, with upregulated gene expression associated with cell functions enriched in cell migration and angiogenesis in ECs and Fibs, and VEGF-driven cell proliferation, apoptotic process and complement activation in SMCs. Interestingly, we discover a novel Fib subtype that mediates type I inflammation in the asthmatic lungs. Moreover, MCs in the asthmatic lungs are found to regulate airway remodeling and immunological responses, with elevated gene expression enriched in cell migration, proliferation, angiogenesis and innate immunological responses. Not only the numbers of epithelial cells in the asthmatic lungs change at the time of lung tissue collection, but also their gene expressions are significantly altered, with an enrichment in the biological processes of IL-17 signaling pathway and apoptosis in the majority of subtypes of epithelial cells. Moreover, the ubiquitin process and DNA repair are more prevalent in ciliated epithelial cells. Last, cell-to-cell interaction analysis reveals a complex network among stromal cells, MCs and macrophages that contribute to the development of asthma and airway remodeling. Our findings provide a critical resource for understanding the principle underlying airway remodeling and inflammation in a monkey model of asthma, as well as valuable hints for the future treatment of asthma, especially the airway remodeling-characterized refractory asthma.

单细胞转录组表征揭示了哮喘猴模型中气道重塑和炎症的全貌。
猴疾病模型在遗传、解剖和生理特征方面与人类相似,对于了解疾病机制和评估生物疗法的效率非常重要。在这里,我们建立了一个由麂皮蝇诱发的哮喘模型,通过单细胞RNA测序(scRNA-seq)来描述肺部气道炎症和重塑。scRNA-seq发现,该模型增加了基质细胞、上皮细胞和间质细胞(MCs)的数量。特别是,该模型增加了肺部内皮细胞(EC)、成纤维细胞(Fib)和平滑肌细胞(SMC)的数量,EC 和 Fib 中与细胞迁移和血管生成相关的细胞功能基因表达上调,SMC 中与血管内皮生长因子驱动的细胞增殖、凋亡过程和补体活化相关的基因表达上调。有趣的是,我们发现了一种新型 Fib 亚型,它在哮喘肺中介导 I 型炎症。此外,我们还发现哮喘病肺中的 MCs 可调节气道重塑和免疫反应,细胞迁移、增殖、血管生成和先天性免疫反应方面的基因表达都有所升高。在采集肺组织时,哮喘患者肺部上皮细胞的数量不仅发生了变化,而且其基因表达也发生了显著改变,在大多数亚型上皮细胞中,IL-17 信号通路和细胞凋亡的生物学过程都有丰富的表达。此外,泛素过程和 DNA 修复在纤毛上皮细胞中更为普遍。最后,细胞间相互作用分析揭示了基质细胞、MCs 和巨噬细胞之间的复杂网络,这种网络有助于哮喘的发展和气道重塑。我们的研究结果为了解猴哮喘模型中气道重塑和炎症的基本原理提供了重要的资源,也为未来治疗哮喘,尤其是以气道重塑为特征的难治性哮喘提供了宝贵的提示。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Materials & Interfaces
ACS Applied Materials & Interfaces 工程技术-材料科学:综合
CiteScore
16.00
自引率
6.30%
发文量
4978
审稿时长
1.8 months
期刊介绍: ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.
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