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Thymic Stromal Lymphopoietin Signaling Pathway Inhibition Attenuates Airway Inflammation and Remodeling in Rats with Asthma

机译:胸腺基质淋巴细胞生成素信号通路抑制可减轻哮喘大鼠的气道炎症和重塑。

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Background/Aims Thymic stromal lymphopoietin (TSLP) is a cytokine that plays diverse roles in the regulation of immune responses. However, a detailed understanding of the TSLP signaling pathway in asthma remains elusive. In this study, we aimed to investigate the role of the TSLP signaling pathway in asthma and its effect on airway inflammation and remodeling. Methods Forty Sprague Dawley (SD) rats were evenly classified into control, asthma, IgG2a mAb and anti-TSLP mAb groups. Ovalbumin (OVA)-induced asthma models were successfully established. Blood, bronchoalveolar lavage fluid (BALF) and lung tissue samples were prepared. Total BALF leukocytes were counted, and the proportions of different leukocyte types were determined. Reverse transcription quantitative polymerase chain reaction (RT-qPCR) and immunohistochemistry were performed to determine the mRNA and protein levels of TSLP, OX40L, α-smooth muscle actin (α-SMA, a marker of airway remodeling in asthma) and collagen I in the plasma. Enzyme-linked immunosorbent assay (ELISA) was carried out to measure the concentrations of TSLP, OX40L, and other inflammatory factors, such as interferon (IFN)-γ, interleukin (IL)-4, IL-5 and IL-13, in the plasma. Results Compared with the control group, there were more leukocytes, increased EOS and LYM proportions, higher Underwood and PAS scores, increased WTt, WTm, WAt/A0, WAm/WAt, WTt/R0, WTm/WTt, TSLP, OX40L, a-SMA and collagen I mRNA and protein levels, and higher SLP, OX40L, IL-4, IL-5 and IL-13 levels, but lower MON proportions and IFN-γ levels in the asthma and IgG2a mAb groups. Compared with the asthma and IgG2a mAb groups, there were less leukocytes, decreased EOS and LYM proportions, lower Underwood and PAS scores, decreased WTt, WTm, WAt/A0, WAm/WAt, WTt/R0, WTm/WTt, TSLP, OX40L, a-SMA and Collagen I mRNA and protein levels, and lower levels of SLP, OX40L, IL-4, IL-5 and IL-13, but higher MON proportions and IFN-γ levels in the anti-TSLP mAb group. WTm and WTt were positively associated with the TSLP, OX40L, α-SMA and collagen-I levels in the rat lung tissues. Conclusion The results indicate that TSLP may be an important contributor for asthma development as TSLP signaling blockade attenuates airway inflammation and remodeling in asthmatic rats.
机译:背景/目的胸腺基质淋巴细胞生成素(TSLP)是一种细胞因子,在免疫应答的调节中起着多种作用。但是,对哮喘中TSLP信号通路的详细了解仍然难以捉摸。在这项研究中,我们旨在研究TSLP信号通路在哮喘中的作用及其对气道炎症和重塑的影响。方法40只SD大鼠随机分为对照组,哮喘组,IgG2a mAb组和抗TSLP mAb组。成功建立卵清蛋白(OVA)诱发的哮喘模型。制备血液,支气管肺泡灌洗液(BALF)和肺组织样本。计算BALF总白细胞,并确定不同白细胞类型的比例。进行逆转录定量聚合酶链反应(RT-qPCR)和免疫组织化学测定TSLP,OX40L,α-平滑肌肌动蛋白(α-SMA,哮喘气道重塑的标志物)和胶原I的mRNA和蛋白水平。等离子体。进行了酶联免疫吸附测定(ELISA)以测量TSLP,OX40L和其他炎症因子的浓度,例如干扰素(IFN)-γ,白介素(IL)-4,IL-5和IL-13。等离子。结果与对照组相比,白细胞增多,EOS和LYM比例增加,Underwood和PAS评分升高,WTt,WTm,WAt / A0,WAm / WAt,WTt / R0,WTm / WTt,TSLP,OX40L,a -哮喘和IgG2a mAb组的-SMA和胶原蛋白I mRNA和蛋白水平较高,SLP,OX40L,IL-4,IL-5和IL-13水平较高,但MON比例和IFN-γ水平较低。与哮喘和IgG2a mAb组相比,白细胞减少,EOS和LYM比例降低,Underwood和PAS评分降低,WTt,WTm,WAt / A0,WAm / WAt,WTt / R0,WTm / WTt,TSLP,OX40L降低,a-SMA和胶原I的mRNA和蛋白质水平,以及SLP,OX40L,IL-4,IL-5和IL-13的水平较低,但抗TSLP mAb组的MON比例和IFN-γ水平较高。 WTm和WTt与大鼠肺组织中的TSLP,OX40L,α-SMA和胶原蛋白I水平呈正相关。结论结果表明TSLP可能是哮喘发展的重要因素,因为TSLP信号传导阻滞减轻了哮喘大鼠的气道炎症和重塑。

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