首页> 外文期刊>European Journal of Immunology >Absence of both Sos-1 and Sos-2 in peripheral CD4+T cells leads to PI3K pathway activation and defects in migration
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Absence of both Sos-1 and Sos-2 in peripheral CD4+T cells leads to PI3K pathway activation and defects in migration

机译:缺乏Sos-1和Sos-2外围CD4 + T细胞导致PI3K途径激活缺陷迁移

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摘要

Sos-1 and Sos-2 are ubiquitously expressed Ras-guanine exchange factors involved in Erk-MAP kinase pathway activation. Using mice lacking genes encoding Sos-1 and Sos-2, we evaluated the role of these proteins in peripheral T-cell signaling and function. Our results confirmed that TCR-mediated Erk activation in peripheral CD4(+) T cells does not depend on Sos-1 and Sos-2, although IL-2-mediated Erk activation does. Unexpectedly, however, we show an increase in AKT phosphorylation in Sos-1/2dKO CD4(+) T cells upon TCR and IL-2 stimulation. Activation of AKT was likely a consequence of increased recruitment of PI3K to Grb2 upon TCR and/or IL-2 stimulation in Sos-1/2dKO CD4(+) T cells. The increased activity of the PI3K/AKT pathway led to downregulation of the surface receptor CD62L in Sos-1/2dKO T cells and a subsequent impairment in T-cell migration.
机译:Sos-1和Sos-2广泛表达参与Erk-MAP Ras-guanine交换因素激酶途径激活。基因编码Sos-1和Sos-2,我们评估了这些蛋白质在周边t细胞的作用信号和功能。在外围TCR-mediated Erk激活CD4 (+) T细胞不依赖于Sos-1和Sos-2,尽管IL-2-mediated Erk激活所做的事。在一种蛋白激酶磷酸化Sos-1/2dKO CD4 (+) T细胞在细胞和刺激- 2。的一种蛋白激酶可能增加的结果招聘的PI3K Grb2识别和/或2刺激Sos-1/2dKO CD4 (+) T细胞。增加活动PI3K / AKT途径导致的表面受体的downregulation CD62LSos-1/2dKO T细胞和随后的障碍t细胞迁移。

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