Trop S, Rhodes M, Wiest D L, Hugo P, Zúñiga-Pflücker J C
Department of Immunology, University of Toronto, Toronto, Ontario, Canada.
J Immunol. 2000 Nov 15;165(10):5566-72. doi: 10.4049/jimmunol.165.10.5566.
During alphabeta T cell development, CD4(-)CD8(-) thymocytes first express pre-TCR (pTalpha/TCR-beta) before their differentiation to the CD4(+)CD8(+) stage. Positive selection of self-tolerant T cells is then determined by the alphabeta TCR expressed on CD4(+)CD8(+) thymocytes. Conceivably, an overlap in surface expression of these two receptors would interfere with the delicate balance of thymic selection. Therefore, a mechanism ensuring the sequential expression of pre-TCR and TCR must function during thymocyte development. In support of this notion, we demonstrate that expression of TCR-alpha by immature thymocytes terminates the surface expression of pre-TCR. Our results reveal that expression of TCR-alpha precludes the formation of pTalpha/TCR-beta dimers within the endoplasmic reticulum, leading to the displacement of pre-TCR from the cell surface. These findings illustrate a novel posttranslational mechanism for the regulation of pre-TCR expression, which may ensure that alphabeta TCR expression on thymocytes undergoing selection is not compromised by the expression of pre-TCR.
在αβ T细胞发育过程中,CD4(-)CD8(-)胸腺细胞在分化为CD4(+)CD8(+)阶段之前首先表达前TCR(pTα/TCR-β)。然后,自我耐受T细胞的阳性选择由CD4(+)CD8(+)胸腺细胞上表达的αβ TCR决定。可以想象,这两种受体在表面表达上的重叠会干扰胸腺选择的微妙平衡。因此,一种确保前TCR和TCR顺序表达的机制必须在胸腺细胞发育过程中发挥作用。为支持这一观点,我们证明未成熟胸腺细胞表达TCR-α会终止前TCR的表面表达。我们的结果表明,TCR-α的表达会阻止内质网内pTα/TCR-β二聚体的形成,导致前TCR从细胞表面位移。这些发现阐明了一种调节前TCR表达的新型翻译后机制,这可能确保正在进行选择的胸腺细胞上的αβ TCR表达不会因前TCR的表达而受到影响。