Ferrick D A, Gajewski D, Mak T W
Ontario Cancer Institute, Department of Medical Biophysics, University of Toronto, Canada.
Adv Exp Med Biol. 1991;292:47-51.
We have determined the fetal expression of V gamma 3, delta and beta TcRs in mice transgenic for the V gamma 1.1J4C gamma 4 TcR chain. The first wave thymocytes appearing at day 14 and disappearing by day 17 in normal mice was absent from the transgenic mice. However, both mice had an almost identical number of gamma delta-bearing thymocytes throughout gestation. Therefore, it is most likely that the V gamma 3J gamma 1C gamma 1 chain was replaced in the transgenic mice by the V gamma 1.1J gamma 4C gamma 4 transgene. The appearance, although slightly earlier for the transgenic mice, of alpha beta-bearing thymocytes was also very similar between transgenic and control mice during gestation. These data suggest that whatever the role of the first wave thymocytes expressing V3-V delta 1 TcRs is, it most likely is not required for the rearrangement, expression and maturation of the alpha beta TcR repertoire. We are currently analyzing a series of gamma delta transgenic mice to determine whether other restricted populations of gamma delta-bearing T cells are involved in specific aspects of immune development or function.
我们已经确定了在转Vγ1.1J4Cγ4 TcR链基因的小鼠中Vγ3、δ和β TcRs的胎儿表达情况。正常小鼠中在第14天出现并在第17天消失的第一波胸腺细胞在转基因小鼠中不存在。然而,在整个妊娠期,两种小鼠中带有γδ的胸腺细胞数量几乎相同。因此,很可能在转基因小鼠中Vγ3Jγ1Cγ1链被Vγ1.1Jγ4Cγ4转基因所取代。在妊娠期,转基因小鼠和对照小鼠中带有αβ的胸腺细胞的出现情况虽然转基因小鼠稍早一些,但也非常相似。这些数据表明,无论表达V3-Vδ1 TcRs的第一波胸腺细胞起什么作用,αβ TcR库的重排、表达和成熟很可能并不需要它。我们目前正在分析一系列γδ转基因小鼠,以确定其他受限的带有γδ的T细胞群体是否参与免疫发育或功能的特定方面。