Carter Immunology Center, University of Virginia, Charlottesville, Virginia, USA.
Nat Immunol. 2010 Feb;11(2):162-70. doi: 10.1038/ni.1830. Epub 2009 Dec 13.
Passage through the beta-selection developmental checkpoint requires productive rearrangement of segments of the T cell antigen receptor-beta gene (Tcrb) and formation of a pre-TCR on the surface of CD4(-)CD8(-) thymocytes. How other receptors influence betabeta-selection is less well understood. Here we define a new role for the chemokine receptor CXCR4 during T cell development. CXCR4 functionally associated with the pre-TCR and influenced beta-selection by regulating the steady-state localization of immature thymocytes in thymic subregions, by facilitating optimal pre-TCR-induced survival signals, and by promoting thymocyte proliferation. We also characterize functionally relevant signaling molecules downstream of CXCR4 and the pre-TCR in thymocytes. Our data designate CXCR4 as a costimulator of the pre-TCR during beta-selection.
通过β选择发育检查点需要 T 细胞抗原受体β 基因(Tcrb)片段的有效重排,并在 CD4(-)CD8(-)胸腺细胞表面形成 pre-TCR。其他受体如何影响β选择尚不清楚。在这里,我们定义了趋化因子受体 CXCR4 在 T 细胞发育过程中的一个新作用。CXCR4 与 pre-TCR 功能相关,并通过调节未成熟胸腺细胞在胸腺区室中的稳态定位、促进最佳的 pre-TCR 诱导的存活信号以及促进胸腺细胞增殖,来影响β选择。我们还鉴定了胸腺细胞中 CXCR4 和 pre-TCR 的下游功能相关信号分子。我们的数据将 CXCR4 指定为β选择期间 pre-TCR 的共刺激因子。