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Spatial transcriptome analysis in the airway epithelium identifies an altered gene expression profile in COPD versus control tissue

转录组 呼吸上皮 慢性阻塞性肺病 基因表达 上皮 气道 基因 计算生物学 生物 细胞生物学 医学 遗传学 内科学 麻醉
作者
Robert J. Hall,Michael A. Portelli,A Clay,Ian P. Hall,Ian Sayers
标识
DOI:10.1183/13993003.congress-2024.pa4400
摘要

Introduction: The airway epithelium is the first line of defence against pathogens and environmental particles, such as cigarette smoke, by acting as a physical barrier and by exerting immunological functions. There is evidence that the airway epithelium is altered in COPD, however spatially resolved studies are lacking on whole lung tissue sections. Spatial transcriptomics has the power to identify genes in lung-relevant region(s) and cell type(s) in tissues from different disease states. Aims: To identify an airway epithelium specific gene expression profile associated with COPD. Methods: Sections of human lung tissue were obtained from lung resection from control donors (n=3) and donors with a diagnosis of COPD (n=3). Slides were hybridised with the GeoMx Human Whole Transcriptome Atlas. Regions of interest were selected (minimum 30 cells, 3 ROI per donor), based on panCK positive fluorescent staining and by tracing around the airway epithelium, from which barcodes were collected, library prepared, and sequenced. Count files were analysed in R using the StandR package and Limma. Results: We identified a specific gene expression profile (FDR 5%) for airway epithelium in COPD tissues versus control (152 genes). Genes enriched by disease state in epithelial regions included cytokeratin genes (KRT5, 15, and 19), which were upregulated in COPD. Conclusion: Our preliminary work has identified a spatially resolved epithelial gene expression profile in COPD lung tissue, including elevated cytokeratin genes, which are major structural proteins of epithelial cells that are essential for tissue integrity.

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