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首页> 外文期刊>BMC Medicine >Germinal center kinase-like kinase (GLK/MAP4K3) expression is increased in adult-onset Still's disease and may act as an activity marker
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Germinal center kinase-like kinase (GLK/MAP4K3) expression is increased in adult-onset Still's disease and may act as an activity marker

机译:在成年性斯蒂尔氏病中,生发中心激酶样激酶(GLK / MAP4K3)的表达增加,并可能作为活性标记

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Background Germinal center kinase-like kinase (GLK, also termed MAP4K3), a member of the MAP4K family, may regulate gene transcription, apoptosis and immune inflammation in response to extracellular signals. The enhanced expression of GLK has been shown to correspond with disease severity in patients with systemic lupus erythematosus. We investigated the role of GLK in the pathogenesis of adult-onset Still's disease, which shares some similar clinical characteristics with systemic lupus erythematosus. Methods The frequencies of circulating GLK-expressing T-cells in 24 patients with active adult-onset Still's disease and 12 healthy controls were determined by flow cytometry analysis. The expression levels of GLK proteins and transcripts were evaluated in peripheral blood mononuclear cells by immunoblotting and quantitative PCR. Serum levels of T helper (Th)17-related cytokines, including IL-1β, IL-6, IL-17 and TNF-α , were measured by ELISA . Results Significantly higher median frequencies of circulating GLK-expressing T-cells were observed in patients with adult-onset Still's disease (31.85%) than in healthy volunteers (8.93%, P P P P P Conclusions Elevated expression levels of GLK and their positive correlation with disease activity in patients with adult-onset Still's disease indicate that GLK may be involved in the pathogenesis and act as a novel activity biomarker of this disease.
机译:背景技术萌发性中心激酶样激酶(GLK,也称为MAP4K3),是MAP4K家族的成员,可响应细胞外信号调节基因转录,凋亡和免疫炎症。已经显示GLK的表达增强与系统性红斑狼疮患者的疾病严重程度相对应。我们调查了GLK在成人性Still病发病机理中的作用,该病与系统性红斑狼疮具有一些相似的临床特征。方法采用流式细胞仪分析24例成年活动性Still病患者和12例健康对照者的表达GLK的T细胞的频率。通过免疫印迹和定量PCR评估外周血单核细胞中GLK蛋白和转录物的表达水平。 ELISA法检测血清T辅助(Th)17相关细胞因子,包括IL-1β,IL-6,IL-17和TNF-α。结果成人成年Still病患者中循环GLK表达T细胞的中位数频率(31.85%)比健康志愿者(8.93%,PPPPP)高。结论GLK的表达水平升高及其与疾病活动的正相关患有成年性斯蒂尔氏病的患者表明,GLK可能参与了发病机理,并成为该病的一种新型活性生物标记物。

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