Aifantis Iannis, Mandal Malay, Sawai Katie, Ferrando Adolfo, Vilimas Tomas
University of Chicago, Department of Medicine, Section of Rheumatology, Committees of Immunology, Cancer and Developmental Biology, Chicago, IL 60637, USA.
Immunol Rev. 2006 Feb;209:159-69. doi: 10.1111/j.0105-2896.2006.00343.x.
Pre-T-cell receptor (pre-TCR) functions and the study of early thymocyte development continue to fascinate immunologists more than 10 years after the first description and cloning of the receptor. Although multiple reports have addressed several aspects of pre-TCR signaling and function, its ability to regulate diverse functions, including proliferation, survival, and allelic exclusion of the TCR-beta locus, remains an open question. What fascinates us is its central role in the fine balance between physiological differentiation and thymocyte transformation that leads to T-cell leukemia and lymphomas. In this review, we integrate pre-TCR signaling pathways and study their effects on the regulation of T-cell progenitor cell-cycle entry and cell survival. We also connect aberrant pre-TCR signaling to deregulated proliferation and apoptotic balances and thymocyte transformation.
在前体T细胞受体(pre-TCR)被首次描述和克隆后的10多年里,pre-TCR的功能以及早期胸腺细胞发育的研究一直吸引着免疫学家。尽管有多项报告探讨了pre-TCR信号传导和功能的多个方面,但其调节多种功能的能力,包括增殖、存活以及TCR-β基因座的等位基因排斥,仍然是一个悬而未决的问题。令我们着迷的是,它在生理分化与导致T细胞白血病和淋巴瘤的胸腺细胞转化之间的精细平衡中起着核心作用。在这篇综述中,我们整合了pre-TCR信号通路,并研究它们对T细胞祖细胞进入细胞周期和细胞存活调节的影响。我们还将异常的pre-TCR信号传导与增殖失控、凋亡平衡失调以及胸腺细胞转化联系起来。