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Chemokines Cytokines and Interleukins: PI3Kgamma (PI3Kγ) is essential for efficient induction of CXCR3 on activated T cells

机译:趋化因子细胞因子和白介素:PI3Kgamma(PI3Kγ)对于在活化T细胞上有效诱导CXCR3是必不可少的

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摘要

The gamma isoform of PI3Kinase (PI3Kγ) controls leukocyte chemotaxis by participating in GPCR signaling, and by regulating cellular polarization. Here we show that PI3Kγ is required for efficient induction of CXC chemokine receptor 3 (CXCR3) on T cells upon activation. T cells from PI3Kγ−/− mice up-regulated CXCR3 less efficiently than wild-type controls both upon activation in vitro as well as during Leishmania mexicana infection. Inhibition of PI3Kinases using wortmannin and or blockade of PI3Kγ activity using a selective inhibitor or PI3Kγ siRNA suppressed induction of CXCR3 on T cells following activation. Levels of CXCR3 and T-bet mRNA were significantly lower in PI3Kγ inhibitor–treated T cells, indicating that PI3Kγ may control CXCR3 expression in part through induction of T-bet. These results reveal a novel role for PI3Kγ in the induction of CXCR3 on T cells and suggest that PI3Kγ may regulate leukocyte chemotaxis by controlling the expression of chemokine receptors.
机译:PI3Kinase(PI3Kγ)的γ亚型通过参与GPCR信号传导和调节细胞极化来控制白细胞趋化性。在这里,我们显示PI3Kγ是激活后在T细胞上有效诱导CXC趋化因子受体3(CXCR3)所必需的。在体外激活以及在墨西哥利什曼原虫感染过程中,PI3Kγ-/-小鼠的T细胞对CXCR3的上调效率均低于野生型对照。使用渥曼青霉素抑制PI3激酶和/或使用选择性抑制剂或PI3KγsiRNA阻断PI3Kγ活性可抑制激活后T细胞对CXCR3的诱导。在PI3Kγ抑制剂处理的T细胞中,CXCR3和T-bet mRNA的水平显着降低,表明PI3Kγ可能部分地通过诱导T-bet来控制CXCR3的表达。这些结果揭示了PI3Kγ在T细胞上诱导CXCR3中的新作用,并暗示PI3Kγ可通过控制趋化因子受体的表达来调节白细胞趋化性。

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