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首页> 外文期刊>Iranian Journal of Immunology >The association between the decreased expression levels of FOXJ1 and the activation of NF-κB pathway in interstitial lung disease of MRL/Lpr mic
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The association between the decreased expression levels of FOXJ1 and the activation of NF-κB pathway in interstitial lung disease of MRL/Lpr mic

机译:MRL / LPR麦克风间质肺病中的表达水平降低与NF-κB途径的激活

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Pulmonary manifestations of systemic lupus erythematosus (SLE) are appearing in 4-5% of patients involving lung in almost half of the cases during the disease course. We compared the autoimmune pulmonary inflammation in the lung tissue of mice to determine the association between decreased expression levels of Forkhead Box J1 (FOXJ1) and the activation of the NF-κB pathway in autoimmune pulmonary inflammation of MRL/Lpr mice. Methods: The female BALB/c mice (n=6) and MRL/Lpr mice (n=30) were divided into 5 groups including a control group (BALB/c), and five MRL/Lpr mice groups (8W, 12W, 16W, 24W, and 32W). The infiltration of the inflammatory cells was determined in lung tissue by performing the histological analysis. The western blotting was used to examine the expression levels of the age-related FOXJ1, and p50 and p65 proteins in the lungs of MRL/Lpr mice. The expression levels of MMP2 and MMP9 were determined via immunohistochemistry and immunofluorescence. Results: There were severe infiltrates of lung cells with high levels of tracheal damage, perivascular injury and interstitial inflammatory cell infiltration when the MRL/Lpr mice from 16w to 32w comparing to the 8w old healthy MRL/Lpr mice in the control group (p<0.05). Moreover, the reduced expression levels of FOXJ1 were associated with the activation of the NF-κB pathway in interstitial lung disease of MRL/Lpr mice via the modulation of p50 and p65. In addition, the expression levels of MMP2 and MMP9 pro-inflammation factors increased in the lungs of the MRL/Lpr mice from 16w to 32w. Conclusions: The expression level of FOXJ1 might be an indicator of the degree of lung disease in lupus-prone mice.
机译:Systemic Lupus红斑(SLE)的肺部表现出现在疾病过程中几乎一半的病例中涉及肺的4-5%的患者。我们比较小鼠的肺组织中的自身免疫性肺炎,以确定叉头箱J1(FoxJ1)的表达水平降低与MRL / LPR小鼠自身免疫肺炎症中NF-κB途径的激活。方法:将雌性BALB / C小鼠(N = 6)和MRL / LPR小鼠(N = 30)分成5组,包括对照组(BALB / C)和5个MRL / LPR小鼠组(8W,12W, 16W,24W和32W)。通过进行组织学分析,在肺组织中测定炎性细胞的渗透。 Western印迹用于检查MRL / LPR小鼠肺中年龄相关的FoxJ1和P50和P65蛋白的表达水平。通过免疫组织化学和免疫荧光测定MMP2和MMP9的表达水平。结果:当与对照组中的8W旧健康MRL / LPR小鼠的16W至32W的MRL / LPR小鼠比较的MRL / LPR小鼠比较的MRL / LPR小鼠时,严重浸润了高水压损伤,血管损伤和间质炎症细胞浸润(P < 0.05)。此外,通过调制P50和P65,FoxJ1的表达水平降低与MRL / LPR小鼠间质肺病中的NF-κB途径的激活相关。此外,MMP2和MMP9促炎因子的表达水平从16W到32W的MRL / LPR小鼠的肺部增加。结论:FoxJ1的表达水平可能是狼疮般小鼠肺病程度的指标。

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