慢性阻塞性肺病基底细胞的分泌细胞与多纤毛细胞失衡,导致对环境压力的恢复能力增强。

IF 9 1区 医学 Q1 RESPIRATORY SYSTEM Thorax Pub Date : 2024-05-20 DOI:10.1136/thorax-2022-219958
Mircea Gabriel Stoleriu, Meshal Ansari, Maximilian Strunz, Andrea Schamberger, Motaharehsadat Heydarian, Yaobo Ding, Carola Voss, Juliane Josephine Schneider, Michael Gerckens, Gerald Burgstaller, Alejandra Castelblanco, Teresa Kauke, Jan Fertmann, Christian Schneider, Juergen Behr, Michael Lindner, Elvira Stacher-Priehse, Martin Irmler, Johannes Beckers, Oliver Eickelberg, Benjamin Schubert, Stefanie M Hauck, Otmar Schmid, Rudolf A Hatz, Tobias Stoeger, Herbert B Schiller, Anne Hilgendorff
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引用次数: 0

摘要

导言:环境污染物会伤害粘膜升降器,从而导致慢性阻塞性肺病(COPD)的病情恶化。人们对健康和疾病中上皮对环境纳米粒子的恢复机制知之甚少:我们研究了流行污染物(如碳和氧化锌纳米粒子)对来自慢性阻塞性肺病晚期(COPD-IV,n=4)、疾病早期(COPD-II,n=3)和肺健康个体(n=4)的原代人类支气管上皮细胞(pHBECs)的细胞功能和后代的影响。pHBECs 在空气-液体界面接触纳米粒子后,细胞培养物通过功能测定、转录组和蛋白质分析进行表征,并对 pHBEC 培养物的序列样本进行单细胞分析,重点关注基础细胞分化:结果:COPD-IV 的特征是分泌表型(MUC5AC+增加了两倍),而多纤毛上皮(Ac-Tub+减少了三倍)则是以牺牲多纤毛上皮为代价的,这导致其对颗粒诱导的细胞损伤的恢复能力增强(跨上皮电阻减少了五倍),环境中大量的氧化锌纳米颗粒就是例证。将 COPD-II 培养物暴露于香烟烟雾提取物会诱发 COPD-IV 特征性的前分泌表型。时间分辨单细胞转录组学揭示了潜在的 COPD-IV 独特基底细胞状态,其特征是 KRT5+ (P=0.018) 和 LAMB3+ (P=0.050) 表达量增加了两倍,Wnt 特异性基因 (P=0.014) 和 Notch 特异性基因 (P=0.021) 被显著激活,尤其是在基底细胞和分泌细胞的前体中:我们在基底细胞中发现了慢性阻塞性肺疾病阶段特异性基因改变,这些改变影响支气管提升器的细胞组成,并可能控制疾病特异性上皮复原机制,以应对环境纳米颗粒。所发现的现象可能会为治疗和预防策略提供依据。
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COPD basal cells are primed towards secretory to multiciliated cell imbalance driving increased resilience to environmental stressors.

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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来源期刊
Thorax
Thorax 医学-呼吸系统
CiteScore
16.10
自引率
2.00%
发文量
197
审稿时长
1 months
期刊介绍: Thorax stands as one of the premier respiratory medicine journals globally, featuring clinical and experimental research articles spanning respiratory medicine, pediatrics, immunology, pharmacology, pathology, and surgery. The journal's mission is to publish noteworthy advancements in scientific understanding that are poised to influence clinical practice significantly. This encompasses articles delving into basic and translational mechanisms applicable to clinical material, covering areas such as cell and molecular biology, genetics, epidemiology, and immunology.
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