Dunne Orla M, Roe Nicola A M, Mousnier Aurélie, Martin S Lorraine, Sergeant Gerard P, About Imad, El-Karim Ikhlas, Lundy Fionnuala T, McGarvey Lorcan P
The Wellcome-Wolfson Institute for Experimental Medicine, School of Medicine, Dentistry and Biomedical Sciences, Queen's University Belfast, 97 Lisburn Road, Belfast, Belfast BT9 7BL, UK.
School of Pharmacy, Queen's University Belfast, Belfast, UK.
Lung. 2025 Sep 7;203(1):93. doi: 10.1007/s00408-025-00846-y.
Rhinovirus (RV) is the leading cause of exacerbations of lung disease. A sensory neuronal model, derived from human dental pulp stem cells and differentiated into peripheral neuronal equivalents (PNEs), was used to examine RV's effects on airway sensory nerves. We investigated whether RV can directly infect and alter PNEs or whether it exerts effects indirectly via the release of mediators from infected epithelial cells.
PNEs or primary bronchial epithelial cells (PBECs) were infected with the RV-A16 strain. Viral replication was confirmed by viral titration assays, immunofluorescence (IF) for the double-stranded RNA (dsRNA) replication intermediate and western blotting (WB). RNA sequencing was used to determine transcriptomic changes in PNEs, and inflammatory responses were assessed by inflammatory microarray. Calcium mobilisation assays were used to investigate the effect of interleukin-1β (IL-1β) on PNE transient receptor potential (TRP) A1 channel responses.
Viral titrations, WB and IF confirm RV-A16 entry and replication in PNEs and PBECs. Gene signatures associated with antiviral immune responses, sensory neuropathies and N-Methyl-D-aspartic acid (NMDA) receptor activity were upregulated in RV infected PNEs. Several cytokines were increased from PNEs and PBECs following RV infection, most notably IL-1β. Treatment of PNEs with IL-1β resulted in heightened TRPA1 channel sensitivity.
We report the suitability of an airway neuronal model for the study of the direct effects of RV infection on nerves. RV-induced release of IL-1β from airway epithelium heightens neuronal TRPA1 responses suggesting a mechanism for virus-induced cough hypersensitivity.
鼻病毒(RV)是肺部疾病加重的主要原因。一种源自人牙髓干细胞并分化为外周神经元等效物(PNE)的感觉神经元模型,被用于研究RV对气道感觉神经的影响。我们研究了RV是否能直接感染并改变PNE,或者它是否通过感染上皮细胞释放介质间接发挥作用。
用RV-A16株感染PNE或原代支气管上皮细胞(PBEC)。通过病毒滴定试验、双链RNA(dsRNA)复制中间体的免疫荧光(IF)和蛋白质印迹法(WB)确认病毒复制。RNA测序用于确定PNE中的转录组变化,炎症反应通过炎症微阵列进行评估。钙动员试验用于研究白细胞介素-1β(IL-1β)对PNE瞬时受体电位(TRP)A1通道反应的影响。
病毒滴定、WB和IF证实RV-A16在PNE和PBEC中进入和复制。在RV感染的PNE中,与抗病毒免疫反应、感觉神经病变和N-甲基-D-天冬氨酸(NMDA)受体活性相关的基因特征上调。RV感染后,PNE和PBEC中几种细胞因子增加,最显著的是IL-1β。用IL-1β处理PNE导致TRPA1通道敏感性增强。
我们报告了一种气道神经元模型适用于研究RV感染对神经的直接影响。RV诱导气道上皮释放IL-1β会增强神经元TRPA1反应,提示病毒诱导咳嗽超敏反应的一种机制。