Brabb T, Rubicz R, Mannikko V, Goverman J
Department of Molecular Biotechnology, University of Washington, Seattle 98195, USA.
Eur J Immunol. 1997 Nov;27(11):3039-48. doi: 10.1002/eji.1830271142.
Two aspects of T cell differentiation in T cell receptor (TCR)-transgenic mice, the generation of an unusual population of CD4-CD8-TCR+ thymocytes and the absence of gamma delta cells, have been the focus of extensive investigation. To examine the basis for these phenomena, we investigated the effects of separate expression of a transgenic TCR alpha chain and a transgenic TCR beta chain on thymocyte differentiation. Our data indicate that expression of a transgenic TCR alpha chain causes thymocytes to differentiate into a CD4-CD8-TCR+ lineage at an early developmental stage, depleting the number of thymocytes that differentiate into the alpha beta lineage. Surprisingly, expression of the TCR alpha chain transgene is also associated with the development of T cell lymphosarcoma. In contrast, expression of the transgenic TCR beta chain causes immature T cells to accelerate differentiation into the alpha beta lineage and thus inhibits the generation of gamma delta cells. Our observations provide a model for understanding T cell differentiation in TCR-transgenic mice.
T细胞受体(TCR)转基因小鼠中T细胞分化的两个方面,即异常的CD4-CD8-TCR+胸腺细胞群体的产生以及γδ细胞的缺失,一直是广泛研究的焦点。为了研究这些现象的基础,我们研究了转基因TCRα链和转基因TCRβ链的单独表达对胸腺细胞分化的影响。我们的数据表明,转基因TCRα链的表达会使胸腺细胞在早期发育阶段分化为CD4-CD8-TCR+谱系,从而减少分化为αβ谱系的胸腺细胞数量。令人惊讶的是,TCRα链转基因的表达还与T细胞淋巴瘤的发展有关。相比之下,转基因TCRβ链的表达会使未成熟T细胞加速分化为αβ谱系,从而抑制γδ细胞的产生。我们的观察结果为理解TCR转基因小鼠中的T细胞分化提供了一个模型。