慢性阻塞性肺疾病伴进行性支气管梗阻患者痰中TRP通道表达及细胞因子谱的特点

D. Naumov, I. Sugaylo, D. Gassan, O. Kotova, Y. Gorchakova, E. Sheludko
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The expression of TRPV1, TRPV4, TRPA1, TRPM8 channels was determined on alveolar macrophages by flow cytometry. Analysis of cytokines was performed in sputum supernatant by multiplex assay on a flow cytometer.Re­sults. It was found that in patients with progressive bronchial obstruction TRPV4 expression was significantly increased: 14.2 (10.8; 23.4)% vs. 8.6 (3.6; 15.4)% (p=0.03). In addition, in the general group of patients a highly significant inverse correlation was found between TRPV4 expression and the dynamics of FEV1 (p=-0.52, p<0.001). Patients with a decrease in FEV1 >50 ml/year were characterized by significantly elevated levels of IL-2, IL-4, IL-17A, IL-10, IL-12p70, CXCL10 and MCP-1. Additionally, we found that concentrations of several cytokines were directly correlated with TRPV4 expres­sion on macrophages: IL-4 (p=0.51, p=0.001), CXCL10 (p=0.59, p<0.001), MCP-1 (p=0.56, p<0.001), TGF-ei (p=0.42, p=0.009), IFN-y (p=0.37, p=0.02).Conclusion. 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摘要

介绍。慢性阻塞性肺疾病(COPD)是一种伴有气道通畅进行性和不可逆恶化的病理。我们知道,呼吸道巨噬细胞积极参与细胞外基质的重组,导致支气管重建的发生。探讨COPD支气管梗阻进展率与肺泡巨噬细胞TRP通道表达及呼吸道炎症标志物水平的关系。材料和方法。该研究招募了37例COPD患者,其中23例FEV1恶化(50 ml/年),14例FEV1下降(50 ml/年),其特征是IL-2、IL-4、IL-17A、IL-10、IL-12p70、CXCL10和MCP-1水平显著升高。此外,我们还发现巨噬细胞中IL-4 (p=0.51, p=0.001)、CXCL10 (p=0.59, p<0.001)、MCP-1 (p=0.56, p<0.001)、TGF-ei (p=0.42, p=0.009)、IFN-y (p=0.37, p=0.02)等细胞因子的浓度与TRPV4的表达有直接关系。肺泡巨噬细胞上表达的TRPV4通道参与COPD的炎症过程和气道重塑,表现为其与某些细胞因子的产生水平以及支气管梗阻进展速度的关系。
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Peculiarities of TRP channels expression and cytokine profile of sputum in patients with chronic obstructive pulmonary disease and progressive bronchial obstruction
Introduction. Chronic obstructive pulmonary disease (COPD) is a pathology accompanied by a pro­gressive and irreversible deterioration in airway patency. It is known that macrophages of the respiratory tract are actively involved in the reorganization of the extracellular matrix leading to the development of bronchial remodeling.Aim. To assess the relationship between the progression rate of bronchial obstruction in COPD, the expression of TRP channels on alveolar macrophages, and the levels of inflammatory markers in the respiratory tract.Materials and methods. The study enrolled 37 patients with COPD, including 23 people with a FEV1 deterioration >50 ml/year and 14 with FEV1 decline <50 ml/year. The expression of TRPV1, TRPV4, TRPA1, TRPM8 channels was determined on alveolar macrophages by flow cytometry. Analysis of cytokines was performed in sputum supernatant by multiplex assay on a flow cytometer.Re­sults. It was found that in patients with progressive bronchial obstruction TRPV4 expression was significantly increased: 14.2 (10.8; 23.4)% vs. 8.6 (3.6; 15.4)% (p=0.03). In addition, in the general group of patients a highly significant inverse correlation was found between TRPV4 expression and the dynamics of FEV1 (p=-0.52, p<0.001). Patients with a decrease in FEV1 >50 ml/year were characterized by significantly elevated levels of IL-2, IL-4, IL-17A, IL-10, IL-12p70, CXCL10 and MCP-1. Additionally, we found that concentrations of several cytokines were directly correlated with TRPV4 expres­sion on macrophages: IL-4 (p=0.51, p=0.001), CXCL10 (p=0.59, p<0.001), MCP-1 (p=0.56, p<0.001), TGF-ei (p=0.42, p=0.009), IFN-y (p=0.37, p=0.02).Conclusion. TRPV4 channels expressed on alveolar macrophages are involved in the inflammatory process and airway remodeling in COPD, which is manifested by their relationships with the level of certain cytokines production, as well as the rate of the progression of bronchial obstruction.
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