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首页> 外文期刊>The journal of immunology >The Rap GTPases Regulate B Cell Migration Toward the Chemokine Stromal Cell-Derived Factor-1 (CXCL12): Potential Role for Rap2 in Promoting B Cell Migration
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The Rap GTPases Regulate B Cell Migration Toward the Chemokine Stromal Cell-Derived Factor-1 (CXCL12): Potential Role for Rap2 in Promoting B Cell Migration

机译:Rap GTPases调节B细胞向趋化因子基质细胞衍生因子1(CXCL12)的迁移:Rap2在促进B细胞迁移中的潜在作用

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摘要

Stromal cell-derived factor-1 (SDF-1) is a potent chemoattractant for B cells and B cell progenitors. Although the binding of SDF-1 to its receptor, CXCR4, activates multiple signaling pathways, the mechanism by which SDF-1 regulates cell migration is not completely understood. In this report we show that activation of the Rap GTPases is important for B cells to migrate toward SDF-1. We found that treating B cells with SDF-1 resulted in the rapid activation of both Rap1 and Rap2. Moreover, blocking the activation of Rap1 and Rap2 via the expression of a Rap-specific GTPase-activating protein significantly reduced the ability of B cells to migrate toward SDF-1. Conversely, expressing a constitutively active form of Rap2 increased SDF-1-induced B cell migration. Thus, the Rap GTPases control cellular processes that are important for B cells to migrate toward SDF-1.
机译:基质细胞衍生因子1(SDF-1)是B细胞和B细胞祖细胞的有效化学引诱剂。尽管SDF-1与其受体CXCR4的结合激活了多个信号传导途径,但SDF-1调节细胞迁移的机制尚未完全了解。在此报告中,我们表明Rap GTPases的激活对于B细胞向SDF-1的迁移很重要。我们发现用SDF-1处理B细胞会导致Rap1和Rap2的快速激活。此外,通过Rap特异性GTPase激活蛋白的表达来阻断Rap1和Rap2的激活,显着降低了B细胞向SDF-1迁移的能力。相反,表达Rap2的组成型活性形式会增加SDF-1诱导的B细胞迁移。因此,Rap GTPases控制对于B细胞向SDF-1迁移很重要的细胞过程。

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