Shinkai Y, Koyasu S, Nakayama K, Murphy K M, Loh D Y, Reinherz E L, Alt F W
Howard Hughes Medical Institute, Children's Hospital, Boston, MA 02115.
Science. 1993 Feb 5;259(5096):822-5. doi: 10.1126/science.8430336.
Introduction of TCR alpha transgene, TCR beta transgene, or both into RAG-2-/-mice differentially rescues T cell development. RAG-2-/- mice have small numbers of TCR-CD4-CD8-(double negative, DN) thymocytes that express CD3 gamma delta epsilon and zeta proteins intracellularly. Introduction of a TCR beta transgene, but not a TCR alpha transgene, into the RAG-2-/- background restored normal numbers of thymocytes. These cells were CD4+CD8+ (double positive, DP) and expressed small amounts of surface TCR beta chain dimers in association with CD3 gamma delta epsilon but not zeta. RAG-2-/- mice that expressed alpha and beta TCR transgenes developed both DP and single positive thymocytes. Thus, the TCR beta subunit, possibly in association with a novel CD3 complex, participates in the DN to the DP transition.
将TCRα转基因、TCRβ转基因或两者导入RAG-2基因敲除小鼠中,对T细胞发育的挽救作用存在差异。RAG-2基因敲除小鼠有少量TCR-CD4-CD8-(双阴性,DN)胸腺细胞,这些细胞在细胞内表达CD3γδε和ζ蛋白。将TCRβ转基因而非TCRα转基因导入RAG-2基因敲除背景中,可恢复胸腺细胞的正常数量。这些细胞为CD4+CD8+(双阳性,DP),并与CD3γδε而非ζ共同表达少量表面TCRβ链二聚体。表达α和βTCR转基因的RAG-2基因敲除小鼠同时发育出双阳性和单阳性胸腺细胞。因此,TCRβ亚基可能与一种新的CD3复合物共同参与了从双阴性到双阳性的转变。