Dave V P, Cao Z, Browne C, Alarcon B, Fernandez-Miguel G, Lafaille J, de la Hera A, Tonegawa S, Kappes D J
Institute for Cancer Research, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.
EMBO J. 1997 Mar 17;16(6):1360-70. doi: 10.1093/emboj/16.6.1360.
The CD3 complex found associated with the T cell receptor (TCR) is essential for signal transduction following TCR engagement. During T cell development, TCR-mediated signalling promotes the transition from one developmental stage to the next and controls whether a thymocyte undergoes positive or negative selection. The roles of particular CD3 components in these events remain unclear. Indeed, it is unknown whether they have specialized or overlapping roles. However, the multiplicity of CD3 components and their evolutionary conservation suggest that they serve distinct functions. Here the developmental requirement for the CD3 delta chain is analyzed by generating a mouse line specifically lacking this component (delta-/- mice). Strikingly, CD3 delta is shown to be differentially required during development. In particular, CD3 delta is not needed for steps in development mediated by pre-TCR or gamma delta TCR, but is required for further development of thymocytes expressing alpha beta TCR. Absence of CD3 delta specifically blocks the thymic selection processes that mediate the transition from the double-positive to single-positive stages of development.
与T细胞受体(TCR)相关的CD3复合物对于TCR结合后的信号转导至关重要。在T细胞发育过程中,TCR介导的信号传导促进从一个发育阶段向下一个阶段的转变,并控制胸腺细胞是经历阳性选择还是阴性选择。特定CD3成分在这些事件中的作用仍不清楚。实际上,它们是否具有专门的或重叠的作用尚不清楚。然而,CD3成分的多样性及其进化保守性表明它们发挥着不同的功能。在此,通过构建一个特异性缺乏该成分的小鼠品系(δ-/-小鼠)来分析CD3δ链在发育中的需求。令人惊讶的是,CD3δ在发育过程中的需求存在差异。特别是,在由前TCR或γδTCR介导的发育步骤中不需要CD3δ,但表达αβTCR的胸腺细胞的进一步发育需要CD3δ。CD3δ的缺失特异性地阻断了介导从双阳性到单阳性发育阶段转变的胸腺选择过程。