Kirberg J, Brocker T
Basel Institute for Immunology, Switzerland.
Int Immunol. 1996 Nov;8(11):1743-9. doi: 10.1093/intimm/8.11.1743.
CD4+ CD8+ double-positive thymocytes differentiate into CD4+ and CD8+ single-positive T cells during thymic positive selection. This process requires the interaction between the TCR and self MHC molecules. In this context we have analyzed the expression of CD45, an abundant transmembrane protein tyrosine phosphatase, and describe here its differential surface expression during T cell maturation. Using four-color FACS analysis of thymocytes from normal as well as TCR-transgenic mice we demonstrate that CD45 is up-regulated only during positive selection concomitantly with the TCR-CD3 complex and the transient early activation marker CD69, but that this up-regulation precedes heat stable antigen down-regulation. The tight linkage of the up-regulation of the TCR-CD3 complex and CD45 may be required because the CD45 tyrosine phosphatase plays a role in modulating signal transduction by the TCR-CD3 complex during positive selection. In addition, our findings argue for a regulation mechanism that adapts the CD45 levels to increasing antigen receptor levels on mature T cells and B cells.
在胸腺阳性选择过程中,CD4⁺CD8⁺双阳性胸腺细胞分化为CD4⁺和CD8⁺单阳性T细胞。这一过程需要TCR与自身MHC分子之间的相互作用。在此背景下,我们分析了CD45(一种丰富的跨膜蛋白酪氨酸磷酸酶)的表达,并在此描述其在T细胞成熟过程中的差异表面表达。通过对来自正常小鼠以及TCR转基因小鼠的胸腺细胞进行四色荧光激活细胞分选分析,我们证明CD45仅在阳性选择期间与TCR-CD3复合物以及瞬时早期激活标志物CD69同时上调,但这种上调先于热稳定抗原下调。TCR-CD3复合物和CD45的上调紧密相关可能是必要的,因为CD45酪氨酸磷酸酶在阳性选择期间调节TCR-CD3复合物的信号转导中发挥作用。此外,我们的研究结果支持一种调节机制,该机制使CD45水平适应成熟T细胞和B细胞上不断增加的抗原受体水平。