Ito K, Bonneville M, Takagaki Y, Nakanishi N, Kanagawa O, Krecko E G, Tonegawa S
Howard Hughes Medical Institute, Massachusetts Institute of Technology, Cambridge 02139.
Proc Natl Acad Sci U S A. 1989 Jan;86(2):631-5. doi: 10.1073/pnas.86.2.631.
We have analyzed the structural diversity of the murine gamma delta T-cell receptor (TCR) heterodimer expressed on CD4- CD8- thymocyte populations and on TCR gamma delta-expressing hybridomas derived from thymocytes of fetal, newborn, and adult mice. We found that CD4- CD8- thymocytes derived from mice of different pre- and postnatal age preferentially express a gamma delta TCR encoded by different subsets of gamma and delta gene segments. This age-dependent differential expression of gamma delta TCR on thymocytes seems to be accomplished in part by a specific control of rearranged gamma genes operating at the level of transcription and/or RNA stability. We discuss the implications of these findings with respect to the recognition roles of the gamma delta TCR.
我们分析了在CD4-CD8-胸腺细胞群体以及源自胎儿、新生和成年小鼠胸腺细胞的表达TCRγδ的杂交瘤上表达的小鼠γδT细胞受体(TCR)异二聚体的结构多样性。我们发现,来自不同产前和产后年龄小鼠的CD4-CD8-胸腺细胞优先表达由γ和δ基因片段的不同亚组编码的γδTCR。胸腺细胞上γδTCR的这种年龄依赖性差异表达似乎部分是通过在转录和/或RNA稳定性水平上对重排γ基因的特定控制来实现的。我们讨论了这些发现对于γδTCR识别作用的意义。