Smoking shifts human small airway epithelium club cells toward a lesser differentiated population

• Published in: Npj genomic medicine Vol. 6; no. 1; p. 73
• Main Authors: Rostami, Mahboubeh R., LeBlanc, Michelle G., Strulovici-Barel, Yael, Zuo, Wulin, Mezey, Jason G., O’Beirne, Sarah L., Kaner, Robert J., Leopold, Philip L., Crystal, Ronald G.
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 08-09-2021; Nature Publishing Group; Nature Portfolio
• Subjects: 692/4017; 692/53; Bioinformatics; Biomedical and Life Sciences; Biomedicine; Cell differentiation; Cigarette smoking; Cyclins; Effector cells; Epithelium; ETS protein; Gene Function; Gene Therapy; Human Genetics; Internal Medicine; Mitochondria; Population; Respiratory tract; Ribosomal proteins; Smoking
• ISSN: 2056-7944; 2056-7944
• DOI: 10.1038/s41525-021-00237-1

The club cell, a small airway epithelial (SAE) cell, plays a central role in human lung host defense. We hypothesized that subpopulations of club cells with distinct functions may exist. The SAE of healthy nonsmokers and healthy cigarette smokers were evaluated by single-cell RNA sequencing, and unsupervised clustering revealed subpopulations of SCGCB1A1
+
KRT5
lo
MUC5AC
−
club cells. Club cell heterogeneity was supported by evaluations of SAE tissue sections, brushed SAE cells, and in vitro air–liquid interface cultures. Three subpopulations included: (1) progenitor; (2) proliferating; and (3) effector club cells. The progenitor club cell population expressed high levels of mitochondrial, ribosomal proteins, and KRT5 relative to other club cell populations and included a differentiation branch point leading to mucous cell production. The small proliferating population expressed high levels of cyclins and proliferation markers. The effector club cell cluster expressed genes related to host defense, xenobiotic metabolism, and barrier functions associated with club cell function. Comparison of smokers vs. nonsmokers demonstrated that smoking limited the extent of differentiation of all three subclusters and altered SAM pointed domain-containing Ets transcription factor (SPDEF)-regulated transcription in the effector cell population leading to a change in the location of the branch point for mucous cell production, a potential explanation for the concomitant reduction in effector club cells and increase in mucous cells in smokers. These observations provide insights into both the makeup of human SAE club cell subpopulations and the smoking-induced changes in club cell biology.