A potential role for CD69 in thymocyte emigration

被引:122
作者
Feng, CG
Woodside, KJ
Vance, BA
El-Khoury, D
Canelles, M
Lee, J
Gress, R
Fowlkes, BJ
Shores, EW
Love, PE [1 ]
机构
[1] NICHHD, Lab Mammalian Genes & Dev, NIH, Bethesda, MD 20892 USA
[2] NCI, Expt Transplantat & Immunol Branch, NIH, Bethesda, MD 20892 USA
[3] NIAID, Lab Mol & Cellular Immunol, NIH, Bethesda, MD 20892 USA
[4] US FDA, Div Hematol Prod, Ctr Biol Evaluat & Res, Bethesda, MD 20892 USA
关键词
CD69; antigen; development; lymphocyte activation; transgenes;
D O I
10.1093/intimm/dxf020
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:535 / 544
页数:10
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