Christmas S E
Department of Immunology, Paterson Institute for Cancer Research, Christie Hospital & Holt Radium Institute, Manchester, United Kingdom.
Cell Immunol. 1989 Nov;124(1):1-12. doi: 10.1016/0008-8749(89)90107-x.
T cell receptor (TCR) gamma gene rearrangements were examined in panels of human T cell clones expressing TCR alpha/beta or gamma/delta heterodimers. Over half of the alpha/beta+ clones had both chromosomes rearranged to C gamma 2 but this was the case for only 20% of the gamma/delta+ clones. While more than half of the gamma/delta+ clones showed a V9JP rearrangement, this configuration was absent from all 49 alpha/beta+ clones analysed. However, this was not a result of all rearrangements being to the more 3' J gamma genes as 11 alpha/beta+ clones had rearrangement(s) to JP1, the most 5' J gamma gene segment. Both alpha/beta+ and gamma/delta+ clones showed a similar pattern of V gamma gene usage in rearrangements to J gamma 1 or J gamma 2 with a lower proportion of the more 3' genes being rearranged to J gamma 2 than for the more 5' genes. Several alpha/beta+ and several gamma/delta+ clones had noncoordinate patterns of rearrangement involving both C gamma 1 and C gamma 2. Eleven out of fourteen CD8+ clones tested had both chromosomes rearranged to C gamma 2 whereas all clones derived from CD4-8- cells and having unconventional phenotypes (CD4-8- or CD4+8+) had at least one C gamma 1 rearrangement. Twelve out of twenty-seven CD4+ clones also had this pattern, suggesting that CD4-8+ clones had a tendency to utilize more 3' J gamma gene segments than CD4+ clones. There was some evidence for interdonor variation in the proportions of TCR gamma rearrangements to C gamma 1 or C gamma 2 in alpha/beta+ clones as well as gamma/delta+ clones. The results illustrate the unique nature of the V9JP rearrangement in gamma/delta+ clones and the possible use of a sequential mechanism of TCR gamma gene rearrangements during T cell differentiation is discussed.
在表达T细胞受体(TCR)α/β或γ/δ异二聚体的人T细胞克隆组中检测了TCRγ基因重排。超过一半的α/β⁺克隆的两条染色体都重排到了Cγ2,但γ/δ⁺克隆中只有20%是这种情况。虽然超过一半的γ/δ⁺克隆显示出V9JP重排,但在分析的所有49个α/β⁺克隆中都没有这种构型。然而,这并不是所有重排都发生在更靠3'端的Jγ基因上的结果,因为有11个α/β⁺克隆重排到了JP1,即最靠5'端的Jγ基因片段。α/β⁺和γ/δ⁺克隆在重排到Jγ1或Jγ2时显示出相似的Vγ基因使用模式,与更靠5'端的基因相比,重排到Jγ2的更靠3'端基因的比例更低。几个α/β⁺和几个γ/δ⁺克隆具有涉及Cγ1和Cγ2的不协调重排模式。在检测的14个CD8⁺克隆中,有11个克隆的两条染色体都重排到了Cγ2,而所有来自CD4⁻8⁻细胞且具有非常规表型(CD4⁻8⁻或CD4⁺8⁺)的克隆至少有一次Cγ1重排。27个CD4⁺克隆中有12个也有这种模式,这表明CD4⁻8⁺克隆比CD4⁺克隆有更多利用更靠3'端Jγ基因片段的倾向。有一些证据表明,α/β⁺克隆以及γ/δ⁺克隆中TCRγ重排到Cγ1或Cγ2的比例存在供体间差异。结果说明了γ/δ⁺克隆中V9JP重排的独特性质,并讨论了在T细胞分化过程中TCRγ基因重排可能使用的顺序机制。