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PAK4 suppresses TNF-induced release of endothelial microparticles in HUVECs cells

机译:Pak4抑制HUVECS细胞中的TNF诱导的内皮微粒释放

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摘要

Tumor necrosis factor-α (TNF) is a pro-inflammatory cytokine upregulated in many inflammatory diseases, and a potent inducer of endothelial cell-derived microparticle (EMP) formation. In this study, we identified the protein kinase PAK4 as a key regulator of the TNF-induced EMP release from human umbilical vein endothelial cells (HUVECs). TNF induces dose- and time-dependent EMP release and downregulation of PAK4 and upstream cdc42 in HUVECs. PAK4 suppression or inhibition of its kinase activity increases TNF-induced EMP release and apoptosis in HUVECs, while PAK4 overexpression reduces EMP release and apoptosis in TNF-stimulated cells. Collectively, these data indicate that PAK4 suppresses TNF-induced EMP generation occurring during apoptosis, and suggest that modulation of PAK4 activity may represent a novel approach to suppress the TNF-induced EMP levels in pro-inflammatory disorders and other pathological conditions.
机译:肿瘤坏死因子-α(TNF)是在许多炎症疾病中上调的促炎细胞因子,以及内皮细胞衍生的微粒(EMP)形成的有效诱导剂。在这项研究中,我们将蛋白激酶Pak4鉴定为从人脐静脉内皮细胞(HUVEC)的TNF诱导的EMP释放的关键调节器。 TNF在Huvecs中诱导PAK4和上游CDC42的剂量和时间依赖的EMP释放和下调。 Pak4抑制或抑制其激酶活性会增加TNF诱导的HUVECS的EMP释放和细胞凋亡,而PAK4过表达在TNF刺激细胞中降低了EMP释放和凋亡。总的来说,这些数据表明,PAK4抑制了在凋亡期间发生的TNF诱导的EMP生成,并表明PAK4活性的调节可以代表一种抑制促炎症紊乱和其他病理条件中TNF诱导的EMP水平的新方法。

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