Feng Chiguang, Woodside Kenneth J, Vance Barbara A, El-Khoury Dalal, Canelles Matilde, Lee Jan, Gress Ronald, Fowlkes B J, Shores Elizabeth W, Love Paul E
Laboratory of Mammalian Genes and Development, National Institute of Child Health and Human Development, Bethesda, MD 20892, USA.
Int Immunol. 2002 Jun;14(6):535-44. doi: 10.1093/intimm/dxf020.
The early activation marker, CD69, is transiently expressed on activated mature T cells and on thymocytes that are undergoing positive or negative selection in the thymus. CD69 is a member of the NK gene complex family of C-type lectin-like signaling receptors; however, its function is unknown. In this report, we describe the characterization of mice that constitutively express high levels of surface CD69 on immature and mature T cells throughout development. Constitutive surface expression of CD69 did not affect T cell maturation, signaling through the TCR or thymocyte selection. However, phenotypically and functionally mature thymocytes accumulated in the medulla of CD69 transgenic mice and failed to be exported from the thymus. The retention of mature thymocytes correlated with transgene dose and CD69 surface levels. These results identify a potential role for CD69 in controlling thymocyte export, and suggest that the transient expression of CD69 on thymocytes and T cells may function to regulate thymocyte and T cell trafficking.
早期激活标志物CD69在活化的成熟T细胞以及在胸腺中正在经历阳性或阴性选择的胸腺细胞上短暂表达。CD69是C型凝集素样信号受体的NK基因复合体家族的成员;然而,其功能尚不清楚。在本报告中,我们描述了在整个发育过程中未成熟和成熟T细胞上组成性表达高水平表面CD69的小鼠的特征。CD69的组成性表面表达不影响T细胞成熟、通过TCR的信号传导或胸腺细胞选择。然而,表型和功能成熟的胸腺细胞积聚在CD69转基因小鼠的髓质中,并且未能从胸腺输出。成熟胸腺细胞的滞留与转基因剂量和CD69表面水平相关。这些结果确定了CD69在控制胸腺细胞输出中的潜在作用,并表明CD69在胸腺细胞和T细胞上的短暂表达可能起到调节胸腺细胞和T细胞运输的作用。