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Cytokine Profile of Human Abdominal Aortic Aneurysm: Involvement of JAK/STAT Pathway

机译:人腹部主动脉瘤的细胞因子概况:JAK / STAT通路的参与。

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摘要

>Objective: Abdominal aortic aneurysm (AAA) is characterized by inflammation and destruction of normal tissue architecture. The present study aimed to evaluate the inflammatory signaling cascade by analyzing the cytokines of AAA tissue.>Materials and Methods: We analyzed the comprehensive cytokine secretion profiles of 52 cytokines from human AAA in four patients with AAA using fluorescent beads-based multiplex assay. Further, the effect of janus kinase (JAK) inhibition by pyridone 6 on cytokine profiles was also evaluated.>Results: Cytokine secretion profiles were found to be similar among the four patients. A high level of JAK/signal transducers and activator of transcription (STAT) pathway activity in AAA tissue in culture was maintained, which may be attributed to the secretion of endogenous JAK-activating cytokines. Inhibition of JAK by pyridone 6 resulted in the suppression of STAT3 phosphorylation and secretion of a subset of chemokines and JAK-activating cytokines. However, the inhibition of JAK had no effect on the secretion of matrix metalloproteinase (MMP)-2, MMP-9, or TGF-β family that is responsible for the metabolism of extracellular matrix.>Conclusion: The findings of the present study suggested that AAA tissue exhibits a stereotypical profile of cytokine secretion, where JAK/STAT pathway may play a role in regulating a subset of cytokines. Identification of such a cytokine profile may reveal potential diagnostic markers and therapeutic targets for AAA.
机译:>客观:腹主动脉瘤(AAA)的特征在于炎症和正常组织结构的破坏。本研究旨在通过分析AAA组织的细胞因子来评估炎症信号的级联反应。>材料和方法:我们使用荧光珠分析了4名AAA患者中人AAA的52种细胞因子的综合细胞因子分泌谱。多重分析。此外,还评估了吡啶酮6抑制janus激酶(JAK)对细胞因子谱的影响。>结果:四名患者的细胞因子分泌谱相似。在培养的AAA组织中维持了高水平的JAK /信号转导子和转录激活剂(STAT)通路活性,这可能归因于内源性JAK激活细胞因子的分泌。吡啶酮6对JAK的抑制导致STAT3磷酸化的抑制以及趋化因子和JAK激活细胞因子的一部分的分泌。然而,抑制JAK对负责细胞外基质代谢的基质金属蛋白酶(MMP)-2,MMP-9或TGF-β家族的分泌没有影响。>结论:本研究的发现表明,AAA组织表现出细胞因子分泌的刻板印象,其中JAK / STAT途径可能在调节细胞因子的子集中起作用。此类细胞因子谱的鉴定可能揭示AAA的潜在诊断标记和治疗靶标。

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