von Boehmer H, Aifantis I, Azogui O, Feinberg J, Saint-Ruf C, Zober C, Garcia C, Buer J
Institut Necker, INSERM U373, Faculté de Médecine, Necker-Enfants-Malades, Paris, France.
Immunol Rev. 1998 Oct;165:111-9. doi: 10.1111/j.1600-065x.1998.tb01234.x.
The analysis of T-cell receptor (TCR) beta selection, TCR beta allelic exclusion and TCR beta rearrangement in gamma delta T cells from normal and pre-TCR-deficient mice has shown that the pre-TCR has a crucial role in T-lymphocyte development: The pre-TCR is by far the most effective receptor that generates large numbers of CD4+8+ T cells with productive TCR beta rearrangements. In the absence of the pre-TCR, TCR beta rearrangement proceeds in developing cells irrespective of whether they already contain a productive TCR beta gene. The pre-TCR directs developing T cells to the alpha beta lineage because gamma delta T cells from pT alpha-/- mice proceed much further in TCR beta rearrangement than gamma delta T cells from wild-type mice. It is argued that the pre-TCR commits developing T cells to the alpha beta lineage by an instructive mechanism, which has largely replaced an evolutionarily more ancient mechanism that involves stochastic alpha beta lineage commitment.
对正常小鼠和前T细胞受体缺陷小鼠的γδ T细胞中T细胞受体(TCR)β链选择、TCR β等位基因排斥和TCR β重排的分析表明,前TCR在T淋巴细胞发育中起关键作用:前TCR是迄今为止最有效的受体,能产生大量具有功能性TCR β重排的CD4+8+ T细胞。在前TCR缺失的情况下,TCR β重排在发育中的细胞中继续进行,而不管它们是否已经含有功能性TCR β基因。前TCR将发育中的T细胞导向αβ谱系,因为来自pTα-/-小鼠的γδ T细胞在TCR β重排中比来自野生型小鼠的γδ T细胞进展得更远。有人认为,前TCR通过一种指导性机制使发育中的T细胞定向到αβ谱系,这种机制在很大程度上取代了一种进化上更古老的机制,即随机的αβ谱系定向。