COPD basal cells are primed towards secretory to multiciliated cell imbalance driving increased resilience to environmental stressors

转录组 慢性阻塞性肺病 基础(医学) 细胞生物学 细胞 医学 免疫学 病理 生物 内科学 基因表达 基因 生物化学 胰岛素
作者
Mircea Gabriel Stoleriu,Meshal Ansari,Maximilian Strunz,Andrea C. Schamberger,Motaharehsadat Heydarian,Yaobo Ding,Carola Voss,Jeremy Schneider,Michael Gerckens,Gerald Burgstaller,Alejandra Castelblanco,Teresa Kauke,Jan Fertmann,Christian Schneider,Jürgen Behr,Michael Lindner,Elvira Stacher‐Priehse,Martin Irmler,Johannes Beckers,Oliver Eickelberg,Benjamin Schubert,Stefanie M. Hauck,Otmar Schmid,Rudolf Hatz,Tobias Stoeger,Herbert B. Schiller,Anne Hilgendorff
出处
期刊:Thorax [BMJ]
卷期号:: thorax-219958
标识
DOI:10.1136/thorax-2022-219958
摘要

Introduction Environmental pollutants injure the mucociliary elevator, thereby provoking disease progression in chronic obstructive pulmonary disease (COPD). Epithelial resilience mechanisms to environmental nanoparticles in health and disease are poorly characterised. Methods We delineated the impact of prevalent pollutants such as carbon and zinc oxide nanoparticles, on cellular function and progeny in primary human bronchial epithelial cells (pHBECs) from end-stage COPD (COPD-IV, n=4), early disease (COPD-II, n=3) and pulmonary healthy individuals (n=4). After nanoparticle exposure of pHBECs at air–liquid interface, cell cultures were characterised by functional assays, transcriptome and protein analysis, complemented by single-cell analysis in serial samples of pHBEC cultures focusing on basal cell differentiation. Results COPD-IV was characterised by a prosecretory phenotype (twofold increase in MUC5AC + ) at the expense of the multiciliated epithelium (threefold reduction in Ac-Tub + ), resulting in an increased resilience towards particle-induced cell damage (fivefold reduction in transepithelial electrical resistance), as exemplified by environmentally abundant doses of zinc oxide nanoparticles. Exposure of COPD-II cultures to cigarette smoke extract provoked the COPD-IV characteristic, prosecretory phenotype. Time-resolved single-cell transcriptomics revealed an underlying COPD-IV unique basal cell state characterised by a twofold increase in KRT5 + ( P =0.018) and LAMB3 + ( P =0.050) expression, as well as a significant activation of Wnt-specific ( P =0.014) and Notch-specific ( P =0.021) genes, especially in precursors of suprabasal and secretory cells. Conclusion We identified COPD stage-specific gene alterations in basal cells that affect the cellular composition of the bronchial elevator and may control disease-specific epithelial resilience mechanisms in response to environmental nanoparticles. The identified phenomena likely inform treatment and prevention strategies.
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