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The NF-kB regulates the SHP-1 expression in monocytes in congestive heart failure

机译:NF-KB在充血性心力衰竭中调节单核细胞中的SHP-1表达

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It has been shown that functional recovery of patients with acute congestive heart failure (ACHF) after treatment with conventional drugs (CD) is mediated by suppression of inflammation in peripheral blood mononuclear cells. Here, we analyzed gene expression profiles of monocytes from symptomatic ACHF patients (NYHA Class III-IV) before and after pharmacological treatment with CD. The treatment was associated with selective downregulation of "TNFR signaling" and pro-inflammatory mediators CCL5, MIP-1 alpha receptor, CD14, ITGAM, and significant up-regulation of "TNFR signaling" as evidenced by increase in anti-inflammatory factors including NF-kBIA, TNFAIP3 and SHP-1. In monocyte TNF-alpha-stimulated there is a down-regulation of the phosphatase SHP-1 which induces a significant activation of TAK-1/IKK/NF-kB signaling. These findings suggest that the therapeutic impact of CD treatment in symptomatic ACHF includes negative regulation of the NF-kB signaling in monocytes and the improvement of the SHP-1 activity.
机译:已经表明,用常规药物(CD)治疗后急性充血性心力衰竭(ACHF)的患者功能恢复是通过抑制外周血单核细胞的炎症来介导的。在此,我们在用CD的药理学治疗之前和之后分析了来自症状ACHF患者(NYHA类III-IV)的单核细胞的基因表达谱。该处理与选择性下调的“TNFR信号传导”和促炎介质CCL5,MIP-1α受体,CCL5,ITGAM和“TNFR信号传导的显着上调”,如抗炎因子(包括NF)的增加所证明的-kbia,tnfaip3和shp-1。在单核细胞TNF-α刺激的情况下,存在磷酸酶SHP-1的下调,其诱导TAK-1 / IKK / NF-KB信号传导的显着激活。这些发现表明CD治疗在症状ACHF中的治疗影响包括单核细胞中NF-KB信号传导的负调节和SHP-1活性的改善。

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