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Central Role of Protein Kinase C in Constitutive Activation of ERK1/2 and Rac1 in the Malignant Cells of Hairy Cell Leukemia

机译:蛋白激酶C在毛细胞白血病恶性细胞ERK1 / 2和Rac1的组成性激活中的核心作用。

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We have previously identified the presence of Ras/Raf-independent constitutive activation of extracellular signal-regulated kinase (ERK) in the hairy cells (HCs) of hairy cell leukemia. The aim of the present study was to characterize the signaling components involved in this activation and their relationship to the reported activation of Rac1. We found that both Rac1 and ERK activation in HCs are downstream of active Src and protein kinase C (PKC). Inhibition with toxin B showed that Rac1 plays no role in ERK activation in HCs. However, toxin B inhibited p60src and the Rac1-GEF Vav, demonstrating a positive feedback/activation of p60src by Rac1. Treatment with specific small interfering RNA for various PKC isoforms, or with PKC isoform-specific inhibitors, demonstrated a central role for PKC in the constitutive activation of Rac1 and ERK in HCs. PKC and active ERK were mutually associated and co-localized with mitochondria in HCs. Furthermore, active PKC was nitrated on tyrosine, pointing to a reactive oxygen species-dependent mechanism of activation. By being involved in activation of ERK and Rac1, PKC plays roles in both the survival of HCs and in the cytoskeletal dynamics responsible for the distinctive morphology and tissue homing of these cells. Our study therefore describes novel aspects of signaling important for the pathogenesis of hairy cell leukemia.
机译:我们以前已经确定在毛细胞白血病的毛细胞(HCs)中存在Ras / Raf独立的细胞外信号调节激酶(ERK)的组成性激活。本研究的目的是表征参与此激活的信号传导成分及其与Rac1报道的激活的关系。我们发现HCs中的Rac1和ERK激活均在活性Src和蛋白激酶C(PKC)的下游。毒素B的抑制作用表明Rac1在HCs的ERK激活中不起作用。但是,毒素B抑制了p60src和Rac1-GEF Vav,表明Rac1对p60src有积极的反馈/激活作用。对于各种PKC同工型,用特定的小干扰RNA或PKC同工型特异性抑制剂进行治疗,证明PKC在HCs中Rac1和ERK的组成型激活中起着核心作用。在HCs中,PKC和活跃的ERK与线粒体相互关联并共同定位。此外,在酪氨酸上将活性PKC硝化,指出了依赖于活性氧的活化机理。通过参与ERK和Rac1的激活,PKC在HC的存活和负责这些细胞独特形态和组织归巢的细胞骨架动力学中均发挥作用。因此,我们的研究描述了对于毛细胞白血病发病机理重要的信号传导的新方面。

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