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

Author:

Stoleriu Mircea GabrielORCID,Ansari Meshal,Strunz Maximilian,Schamberger Andrea,Heydarian MotaharehsadatORCID,Ding Yaobo,Voss Carola,Schneider Juliane Josephine,Gerckens Michael,Burgstaller Gerald,Castelblanco AlejandraORCID,Kauke Teresa,Fertmann Jan,Schneider Christian,Behr Juergen,Lindner Michael,Stacher-Priehse Elvira,Irmler Martin,Beckers Johannes,Eickelberg Oliver,Schubert Benjamin,Hauck Stefanie MORCID,Schmid Otmar,Hatz Rudolf A,Stoeger Tobias,Schiller Herbert B,Hilgendorff Anne

Abstract

IntroductionEnvironmental 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.MethodsWe 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.ResultsCOPD-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.ConclusionWe 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.

Funder

Helmholtz Foundation and the Helmholtz Zentrum München, Germany

European Union’s Horizon 2020 research and innovation programme

Research Training Group Targets in Toxicology

Stiftung AtemWeg

BMBF

Publisher

BMJ

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