D. Naumov, I. Sugaylo, O. Kotova, D. Gassan, Y. Gorchakova, T. Maltseva
{"title":"慢性阻塞性肺疾病患者巨噬细胞中TRP通道表达水平的比较","authors":"D. Naumov, I. Sugaylo, O. Kotova, D. Gassan, Y. Gorchakova, T. Maltseva","doi":"10.36604/1998-5029-2022-85-37-46","DOIUrl":null,"url":null,"abstract":"Introduction. Macrophages are one of the key cells in the pathogenesis of chronic obstructive pulmonary disease (COPD), mediating the primary immune response and coordinating the further reaction of the immune system upon contact with cigarette smoke and air pollutants. It is known that some TRP channels expressed on macrophages are receptors for dust particles and cigarette smoke components.Aim. To study the features of TRPV1, TRPV4, TRPA1 and TRPM8 channels expression on monocyte-derived macrophages and alveolar macrophages of COPD patients and smokers without bronchial obstruction.Materials and methods. Expression of TRP channels at the mRNA level was studied in monocyte-derived macrophages obtained from 8 COPD patients and 6 healthy smokers by quantitative reverse transcription PCR. Expression of TRP channels at the protein level was studied on alveolar macrophages of 39 COPD patients and 8 healthy smokers by indirect flow cytometry.Results. It was found that under in vitro conditions, monocyte-derive macrophages of COPD patients were distinguished by a significant 4.8-fold increase in the number of TRPV1 transcripts (p=0.009). At the same time, the expression of the TRPV1 protein on the alveolar macrophages of COPD patients was also significantly higher when compared to the cells of smokers from the control group (14.1 [6.4‒21.2]% vs. 6.1 [2.1‒9.8]%, p=0.006). In addition, we found that TRPV4 expression was increased among active smokers with COPD, and the expression of TRPA1 and TRPM8 channels correlated with some lung function parameters.Conclusion. The obtained results suggest that the increased expression of TRPV1 on macrophages may be a marker of the disease and contribute to its development, while the expression of TRPV4, TRPA1 and TRPM8 may influence the clinical course of COPD.","PeriodicalId":9598,"journal":{"name":"Bulletin Physiology and Pathology of Respiration","volume":"104 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-09-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Comparative characteristics of TRP channels expression levels on the macrophages of patients with chronic obstructive pulmonary disease\",\"authors\":\"D. Naumov, I. Sugaylo, O. Kotova, D. Gassan, Y. Gorchakova, T. Maltseva\",\"doi\":\"10.36604/1998-5029-2022-85-37-46\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Introduction. Macrophages are one of the key cells in the pathogenesis of chronic obstructive pulmonary disease (COPD), mediating the primary immune response and coordinating the further reaction of the immune system upon contact with cigarette smoke and air pollutants. It is known that some TRP channels expressed on macrophages are receptors for dust particles and cigarette smoke components.Aim. To study the features of TRPV1, TRPV4, TRPA1 and TRPM8 channels expression on monocyte-derived macrophages and alveolar macrophages of COPD patients and smokers without bronchial obstruction.Materials and methods. Expression of TRP channels at the mRNA level was studied in monocyte-derived macrophages obtained from 8 COPD patients and 6 healthy smokers by quantitative reverse transcription PCR. Expression of TRP channels at the protein level was studied on alveolar macrophages of 39 COPD patients and 8 healthy smokers by indirect flow cytometry.Results. It was found that under in vitro conditions, monocyte-derive macrophages of COPD patients were distinguished by a significant 4.8-fold increase in the number of TRPV1 transcripts (p=0.009). At the same time, the expression of the TRPV1 protein on the alveolar macrophages of COPD patients was also significantly higher when compared to the cells of smokers from the control group (14.1 [6.4‒21.2]% vs. 6.1 [2.1‒9.8]%, p=0.006). In addition, we found that TRPV4 expression was increased among active smokers with COPD, and the expression of TRPA1 and TRPM8 channels correlated with some lung function parameters.Conclusion. The obtained results suggest that the increased expression of TRPV1 on macrophages may be a marker of the disease and contribute to its development, while the expression of TRPV4, TRPA1 and TRPM8 may influence the clinical course of COPD.\",\"PeriodicalId\":9598,\"journal\":{\"name\":\"Bulletin Physiology and Pathology of Respiration\",\"volume\":\"104 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-09-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Bulletin Physiology and Pathology of Respiration\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.36604/1998-5029-2022-85-37-46\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bulletin Physiology and Pathology of Respiration","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.36604/1998-5029-2022-85-37-46","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
摘要
介绍。巨噬细胞是慢性阻塞性肺疾病(chronic obstructive pulmonary disease, COPD)发病机制中的关键细胞之一,介导初次免疫反应,协调接触香烟烟雾和空气污染物后免疫系统的进一步反应。巨噬细胞上表达的一些TRP通道是粉尘颗粒和香烟烟雾成分的受体。研究无支气管梗阻的COPD患者及吸烟者单核细胞源性巨噬细胞及肺泡巨噬细胞中TRPV1、TRPV4、TRPA1、TRPM8通道的表达特征。材料和方法。采用定量反转录PCR方法研究了8例COPD患者和6例健康吸烟者单核细胞源性巨噬细胞中TRP通道mRNA水平的表达。用间接流式细胞术研究了39例COPD患者和8例健康吸烟者肺泡巨噬细胞在蛋白水平上TRP通道的表达。研究发现,在体外条件下,COPD患者单核细胞来源的巨噬细胞的TRPV1转录本数量显著增加4.8倍(p=0.009)。同时,COPD患者肺泡巨噬细胞中TRPV1蛋白的表达也明显高于对照组吸烟者(14.1 [6.4-21.2]% vs. 6.1 [2.1-9.8]%, p=0.006)。此外,我们发现活跃吸烟者COPD患者中TRPV4表达升高,TRPA1和TRPM8通道表达与肺功能参数相关。上述结果提示,巨噬细胞上TRPV1的表达升高可能是疾病的一个标志并参与了疾病的发展,而TRPV4、TRPA1和TRPM8的表达可能影响COPD的临床病程。
Comparative characteristics of TRP channels expression levels on the macrophages of patients with chronic obstructive pulmonary disease
Introduction. Macrophages are one of the key cells in the pathogenesis of chronic obstructive pulmonary disease (COPD), mediating the primary immune response and coordinating the further reaction of the immune system upon contact with cigarette smoke and air pollutants. It is known that some TRP channels expressed on macrophages are receptors for dust particles and cigarette smoke components.Aim. To study the features of TRPV1, TRPV4, TRPA1 and TRPM8 channels expression on monocyte-derived macrophages and alveolar macrophages of COPD patients and smokers without bronchial obstruction.Materials and methods. Expression of TRP channels at the mRNA level was studied in monocyte-derived macrophages obtained from 8 COPD patients and 6 healthy smokers by quantitative reverse transcription PCR. Expression of TRP channels at the protein level was studied on alveolar macrophages of 39 COPD patients and 8 healthy smokers by indirect flow cytometry.Results. It was found that under in vitro conditions, monocyte-derive macrophages of COPD patients were distinguished by a significant 4.8-fold increase in the number of TRPV1 transcripts (p=0.009). At the same time, the expression of the TRPV1 protein on the alveolar macrophages of COPD patients was also significantly higher when compared to the cells of smokers from the control group (14.1 [6.4‒21.2]% vs. 6.1 [2.1‒9.8]%, p=0.006). In addition, we found that TRPV4 expression was increased among active smokers with COPD, and the expression of TRPA1 and TRPM8 channels correlated with some lung function parameters.Conclusion. The obtained results suggest that the increased expression of TRPV1 on macrophages may be a marker of the disease and contribute to its development, while the expression of TRPV4, TRPA1 and TRPM8 may influence the clinical course of COPD.