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Cytokines reprogram airway sensory neurons in asthma. 细胞因子对哮喘中的气道感觉神经元进行了重编程。
Q4 Materials Science Pub Date : 2024-09-18 DOI: 10.1101/2023.01.26.525731
Théo Crosson, Shreyas Bhat, Jo-Chiao Wang, Clara Salaun, Eleanne Fontaine, Katiane Roversi, Herbert Herzog, Moutih Rafei, Rikard Blunck, Sebastien Talbot

Nociceptor neurons play a crucial role in maintaining the body's homeostasis by detecting and responding to potential dangers in the environment. However, this function can be detrimental during allergic reactions, since vagal nociceptors can contribute to immune cell infiltration, bronchial hypersensitivity, and mucus imbalance, in addition to causing pain and coughing. Despite this, the specific mechanisms by which nociceptors acquire pro-inflammatory characteristics during allergic reactions are not yet fully understood. In this study, we aimed to investigate the molecular profile of airway nociceptor neurons during allergic airway inflammation and identify the signals driving such reprogramming. Using retrograde tracing and lineage reporting, we identified a unique class of inflammatory vagal nociceptor neurons that exclusively innervate the airways. In the ovalbumin mouse model of airway inflammation, these neurons undergo significant reprogramming characterized by the upregulation of the NPY receptor Npy1r. A screening of cytokines and neurotrophins revealed that IL-1β, IL-13 and BDNF drive part of this reprogramming. IL-13 triggered Npy1r overexpression in nociceptors via the JAK/STAT6 pathway. In parallel, sympathetic neurons and macrophages release NPY in the bronchoalveolar fluid of asthmatic mice, which limits the excitability of nociceptor neurons. Single-cell RNA sequencing of lung immune cells has revealed that a cell-specific knockout of Npy1r in nociceptor neurons in asthmatic mice leads to an increase in airway inflammation mediated by T cells. Opposite findings were observed in asthmatic mice in which nociceptor neurons were chemically ablated. In summary, allergic airway inflammation reprograms airway nociceptor neurons to acquire a pro-inflammatory phenotype, while a compensatory mechanism involving NPY1R limits nociceptor neurons' activity.

痛觉神经元通过检测和应对环境中的潜在危险,在维持机体平衡方面发挥着至关重要的作用。然而,这种功能在过敏反应期间可能是有害的,因为迷走神经痛觉感受器除了引起疼痛和咳嗽外,还可能导致免疫细胞浸润、支气管过敏和粘液失衡。尽管如此,过敏反应期间痛觉感受器获得促炎特性的具体机制仍未完全明了。在这项研究中,我们旨在研究过敏性气道炎症期间气道痛觉感受器神经元的分子特征,并确定驱动这种重编程的信号。通过逆行追踪和系谱报告,我们发现了一类独特的专门支配气道的炎性迷走神经痛觉神经元。在卵清蛋白小鼠气道炎症模型中,这些神经元发生了显著的重编程,其特征是 NPY 受体 Npy1r 的上调。对细胞因子和神经营养素的筛选显示,IL-1β、IL-13 和 BDNF 驱动了这种重编程的一部分。IL-13通过JAK/STAT6途径在痛觉感受器中引发Npy1r过表达。与此同时,交感神经元和巨噬细胞在哮喘小鼠的支气管肺泡液中释放 NPY,从而限制了痛觉感受器神经元的兴奋性。肺部免疫细胞的单细胞 RNA 测序显示,哮喘小鼠痛觉神经元中 Npy1r 的细胞特异性敲除会导致由 T 细胞介导的气道炎症增加。而对哮喘小鼠的痛觉神经元进行化学消融后,则观察到了相反的结果。总之,过敏性气道炎症重编程气道痛觉神经元,使其获得促炎表型,而涉及 NPY1R 的补偿机制限制了痛觉神经元的活动。
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引用次数: 0
Characteristics analysis and monitoring of friction stir welded dissimilar AA5083/AA6061-T6 using acoustic emission technique 利用声发射技术分析和监测摩擦搅拌焊接异种 AA5083/AA6061-T6 的特性
Q4 Materials Science Pub Date : 2024-07-24 DOI: 10.1080/09507116.2024.2376187
S. Kannaiyan, S. Murugesan, Dhamotharakannan Thirumalaikannan, Balasubramanian Visvalingam, B. P. Nagasai
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引用次数: 0
Edge detection in x-ray images of drill mast welds based on an improved Scharr operator 基于改进型沙尔算子的钻杆焊缝 X 射线图像边缘检测
Q4 Materials Science Pub Date : 2024-07-17 DOI: 10.1080/09507116.2024.2378818
Wenjun Qian
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引用次数: 0
Experimentally validated numerical prediction of laser welding induced distortions of Al alloy parts for railcar body by inherent strain method combined with thermo-elastic-plastic FE model 利用固有应变法结合热塑 FE 模型,对轨道车车体铝合金部件激光焊接诱发变形进行实验验证的数值预测
Q4 Materials Science Pub Date : 2024-06-07 DOI: 10.1080/09507116.2024.2354262
Hongxiao Wang, Chunsheng Wang, Jiancai Di, Zhangqi Yan, Liguo Liu
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引用次数: 0
Understanding of thermal behaviour in keyhole plasma arc welding process through numerical modelling–an overview 通过数值建模了解锁孔等离子弧焊过程中的热行为--综述
Q4 Materials Science Pub Date : 2024-05-14 DOI: 10.1080/09507116.2024.2349917
Kumud Ranjan, Sushovan Basak, Manoj Kr. Gopaliya
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引用次数: 0
Effect of post-weld heat treatment on mechanical and microstructural properties of high strength steel weld metal 焊后热处理对高强度钢焊接金属机械性能和微观结构性能的影响
Q4 Materials Science Pub Date : 2024-05-07 DOI: 10.1080/09507116.2024.2348008
Ebrahim Harati, Ehsan Harati, Uchenna Onochie
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引用次数: 0
A study on effect of laser overlay welding parameters of stainless steel 301 LN: tensile test, microstructure analysis and microhardness evaluation 不锈钢 301 LN 激光堆焊参数的影响研究:拉伸试验、微观结构分析和显微硬度评估
Q4 Materials Science Pub Date : 2024-04-19 DOI: 10.1080/09507116.2024.2342342
Payam Farhadipour, S. Dehghan, N. Barka, Asim Iltaf, Pedram Farhadipour
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引用次数: 0
Investigation of effect of post weld heat treatment on microhardness and microstructure of auto TIG welded stabilized SA213 TP347H weldments 研究焊后热处理对自动氩弧焊稳定化 SA213 TP347H 焊件显微硬度和显微组织的影响
Q4 Materials Science Pub Date : 2024-04-19 DOI: 10.1080/09507116.2024.2342340
Pradip K. Gajjar, Bharat C. Khatri, Rajesh Jha
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引用次数: 0
A critical overview on fracture mechanical characterization on marine grade structural materials and its welds 海洋级结构材料及其焊缝的断裂力学特性分析综述
Q4 Materials Science Pub Date : 2024-04-16 DOI: 10.1080/09507116.2024.2338405
Vysakh Kadayath Bijukumar, Mathiazhagan Andy, Satheesh Babu Perukkavungal Kollerithodiyil, Krishna Prasad Shaji
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引用次数: 0
Wire arc additive manufacturing using high-strength steel tubular and solid wires 使用高强度钢管和实心线材的线弧快速成型技术
Q4 Materials Science Pub Date : 2024-04-15 DOI: 10.1080/09507116.2024.2337163
Ebrahim Harati, Bibu Jose, Mattias Igestrand
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引用次数: 0
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