Department of Internal Medicine, Pulmonary Diseases and Allergy, Medical University of Warsaw, Poland.
Postgraduate School of Molecular Medicine, Medical University of Warsaw, Warsaw, Poland.
Clin Immunol. 2020 Jun;215:108421. doi: 10.1016/j.clim.2020.108421. Epub 2020 Apr 14.
In the respiratory system macrophages and dendritic cells collaborate as sentinels against foreign particulate antigens. The study used a triple-cell co-culture model, utilizing nasal epithelial cells, along with: monocyte derived macrophages (moMφs), and monocyte derived DCs (moDCs). Cell cultures from 15 controls, 14 asthma and 11 COPD patients were stimulated with IL-13 and poly I:C for 24 h. Co-cultivation of epithelial cells with moMφs and moDCs increased TSLP level only in asthma and the effect of IL-13 and poly I:C stimulation differed in all groups. Asthma epithelial cells expressed higher level of receptors TSLPR, ST2 and IL-17RA than controls and increased number of ST2 + ciliated and IL17RA + secretory cells. Cytokine expression in respiratory epithelium may be influenced by structural and immunological cell interaction. TSLP pathway may be associated with secretory, while IL-33 with ciliated cells. The impaired function of respiratory epithelium may impact cell-to-cell interactions in asthma.
在呼吸系统中,巨噬细胞和树突状细胞作为外来颗粒抗原的哨兵协同作用。本研究采用三细胞共培养模型,利用鼻上皮细胞,并结合:单核细胞衍生的巨噬细胞(moMφs)和单核细胞衍生的树突状细胞(moDCs)。来自 15 名对照者、14 名哮喘患者和 11 名 COPD 患者的细胞培养物用 IL-13 和多聚 I:C 刺激 24 小时。上皮细胞与 moMφs 和 moDCs 的共培养仅在哮喘中增加 TSLP 水平,而 IL-13 和多聚 I:C 刺激在所有组中的作用不同。哮喘上皮细胞表达的 TSLPR、ST2 和 IL-17RA 受体水平高于对照组,并且 ST2+ciliated 和 IL17RA+secretory 细胞的数量增加。呼吸道上皮细胞的细胞因子表达可能受结构和免疫细胞相互作用的影响。TSLP 途径可能与分泌有关,而 IL-33 与纤毛细胞有关。呼吸道上皮细胞功能受损可能会影响哮喘中的细胞间相互作用。