Xiong Na, Kang Chuhlo, Raulet David H
Department of Molecular and Cell Biology, 489 Life Sciences Addition, University of California, Berkeley, 94720, USA.
Immunity. 2004 Jul;21(1):121-31. doi: 10.1016/j.immuni.2004.06.008.
The role of cellular selection in the development of gammadelta T cells remains unclear. Knockout mice lacking a subset of Vgamma genes, including Vgamma3, contain abundant gammadelta T cells but are devoid of dendritic epidermal gammadeltaT cells (DETCs), which normally express an invariant Vgamma3/Vdelta1 gammadelta TCR. A rearranged Vgamma2 transgene restored DETC development, but the restored DETCs selectively expressed a unique Vdelta gene other than Vdelta1, indicating that DETC development involves TCR-based selection. In both normal and transgenic/knockout mice, specific DETC precursors in the fetal thymus were activated and expressed the IL-15 receptor beta chain, skin-homing receptors, and thymic exiting receptors. In vitro activation of irrelevant precursors also led to upregulation of the skin-homing receptor, providing an explanation for how thymic selection is coordinated with development of epidermal gammadelta T cells.
细胞选择在γδ T细胞发育中的作用仍不清楚。缺乏包括Vγ3在内的一部分Vγ基因的敲除小鼠含有丰富的γδ T细胞,但缺乏树突状表皮γδ T细胞(DETC),而正常情况下这些细胞表达恒定的Vγ3/Vδ1 γδ TCR。一个重排的Vγ2转基因恢复了DETC的发育,但恢复后的DETC选择性地表达了除Vδ1之外的一个独特的Vδ基因,这表明DETC的发育涉及基于TCR的选择。在正常小鼠和转基因/敲除小鼠中,胎儿胸腺中的特定DETC前体细胞被激活,并表达IL-15受体β链、皮肤归巢受体和胸腺迁出受体。体外激活不相关的前体细胞也会导致皮肤归巢受体上调,这为胸腺选择如何与表皮γδ T细胞的发育相协调提供了解释。