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Respir Res ; 21(1): 200, 2020 Jul 29.
Article in English | MEDLINE | ID: mdl-32727470

ABSTRACT

BACKGROUND: The human small airway epithelium (SAE) plays a central role in the early events in the pathogenesis of most inherited and acquired lung disorders. Little is known about the molecular phenotypes of the specific cell populations comprising the SAE in humans, and the contribution of SAE specific cell populations to the risk for lung diseases. METHODS: Drop-seq single-cell RNA-sequencing was used to characterize the transcriptome of single cells from human SAE of nonsmokers and smokers by bronchoscopic brushing. RESULTS: Eleven distinct cell populations were identified, including major and rare epithelial cells, and immune/inflammatory cells. There was cell type-specific expression of genes relevant to the risk of the inherited pulmonary disorders, genes associated with risk of chronic obstructive pulmonary disease and idiopathic pulmonary fibrosis and (non-mutated) driver genes for lung cancers. Cigarette smoking significantly altered the cell type-specific transcriptomes and disease risk-related genes. CONCLUSIONS: This data provides new insights into the possible contribution of specific lung cells to the pathogenesis of lung disorders.


Subject(s)
Cigarette Smoking/genetics , Genetic Testing/methods , Lung Diseases/genetics , Respiratory Mucosa/physiology , Sequence Analysis, RNA/methods , Transcriptome/genetics , Airway Remodeling/genetics , Bronchoscopy/methods , Cigarette Smoking/adverse effects , Gene Expression , Humans , Lung Diseases/diagnosis , Lung Neoplasms/diagnosis , Lung Neoplasms/genetics , Pulmonary Disease, Chronic Obstructive/diagnosis , Pulmonary Disease, Chronic Obstructive/genetics , Respiratory Mucosa/pathology
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