首页> 外文期刊>Thorax: The Journal of the British Thoracic Society >COPD basal cells are primed towards secretory to multiciliated cell imbalance driving increased resilience to environmental stressors
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COPD basal cells are primed towards secretory to multiciliated cell imbalance driving increased resilience to environmental stressors

机译:COPD 基底细胞为分泌型至多纤毛细胞失衡做好准备,从而提高对环境压力源的适应力

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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.
机译:简介 环境污染物会损伤粘膜纤毛电梯,从而引发慢性阻塞性肺病 (COPD) 的疾病进展。健康和疾病中对环境纳米颗粒的上皮弹性机制描述不佳。方法 我们描述了碳和氧化锌纳米颗粒等普遍污染物对终末期 COPD (COPD-IV, n=4)、早期疾病 (COPD-II, n=3) 和肺部健康个体 (n=4) 的原代人支气管上皮细胞 (pHBECs) 细胞功能和后代的影响。在气液界面处纳米颗粒暴露 pHBEC 后,通过功能测定、转录组和蛋白质分析对细胞培养物进行表征,并辅以 pHBEC 培养物系列样品中的单细胞分析,重点关注基底细胞分化。结果结果COPD-IV 的特征是分泌表型 (MUC5AC+ 增加两倍) 以牺牲多纤毛上皮 (Ac-Tub+ 减少三倍) 为特征,导致对颗粒诱导的细胞损伤的恢复力增加 (跨上皮电阻降低五倍),如环境丰富剂量的氧化锌纳米颗粒所证明。COPD-II 培养物暴露于香烟烟雾提取物会引发 COPD-IV 特征的分泌表型。时间分辨的单细胞转录组学揭示了潜在的 COPD-IV 独特的基底细胞状态,其特征是 KRT5+ 增加两倍 (P=0.018) 和 LAMB3+ (P=0.050) 表达,以及 Wnt 特异性 (P=0.014) 和 Notch 特异性 (P=0.021) 基因的显着激活,尤其是在基底层上细胞和分泌细胞的前体中。结论 我们在基底细胞中发现了 COPD 阶段特异性基因改变,这些改变影响支气管电梯的细胞组成,并可能控制响应环境纳米颗粒的疾病特异性上皮弹性机制。已识别的现象可能为治疗和预防策略提供信息。

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