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Inhibition of T-cell activation by PIK3IP1

机译:由PIK3IP1抑制t细胞的活化

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摘要

The PI-3 kinase (PI3K) pathway is critical for T-cell development and activation. Several negative regulators of this pathway have already been described and characterized: the lipid phosphatases SHIP, inositol polyphosphate-4-phosphatase, type II (INPP4B), and phosphatase and tensin homolog (PTEN), the latter of which are tumor suppressors. PIK3IP1 (PI3K interacting protein 1) is a recently described transmembrane protein that has the ability to bind the catalytic protein p110 and prevent its activation by the p85 family adaptor proteins. Thus far, nothing is known about the possible role of PIK3IP1 in the regulation of lymphocyte development or activation. Here, we show for the first time that PIK3IP1 is expressed in T cells. Ectopic expression of PIK3IP1 in Jurkat or D10 T-cell lines inhibited activation of an NFAT/AP-1 transcriptional reporter. Conversely, siRNA-mediated silencing of PIK3IP1 in the same cell lines modestly augmented Akt phosphorylation, T-cell activation, and production of IL-2. These results suggest that the novel PI3K regulator PIK3IP1 plays an inhibitory role in T-cell activation.
机译:PI-3激酶(PI3K)途径是至关重要的t细胞发育和激活。这个途径的负调控已经被描述和特征:脂质磷酸酶船、肌醇polyphosphate-4-phosphatase, II型(INPP4B),和磷酸酶tensin同族体(PTEN)后者是肿瘤抑制。最近(PI3K蛋白1)交互跨膜蛋白的描述催化蛋白质p110和结合的能力防止其激活p85家族适配器蛋白质。可能的PIK3IP1在调节中的作用淋巴细胞发展或激活。第一次展示PIK3IP1表示在T细胞。Jurkat或D10抑制激活t细胞线NFAT / AP-1转录的记者。相反,siRNA-mediated PIK3IP1沉默在同一个细胞系小幅增强一种蛋白激酶磷酸化、t细胞活化和- 2的生产。这部小说PI3K监管者PIK3IP1扮演在t细胞活化的抑制作用。

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