Garman R D, Ko J L, Vulpe C D, Raulet D H
Proc Natl Acad Sci U S A. 1986 Jun;83(11):3987-91. doi: 10.1073/pnas.83.11.3987.
We have examined T-cell receptor alpha- and beta-chain variable (V) region gene usage in T-cell populations predicted to have different major histocompatibility complex-restriction specificities. Using a sensitive ribonuclease protection assay to measure T-cell receptor mRNA levels, we found no striking differences in the usage of three V alpha genes and three V beta genes in T-cell populations from three congeneic H-2-disparate strains of mice and between the mutually exclusive Ly2+ L3T4- and Ly2- L3T4+ T-cell subpopulations. These results suggest that major histocompatibility complex restriction cannot be explained by the differential usage of nonoverlapping V alpha or V beta gene pools. In contrast, striking but unpredictable differences were seen in V gene usage in populations of T cells selected by activation with particular alloantigens.
我们研究了预计具有不同主要组织相容性复合体限制特异性的T细胞群体中T细胞受体α链和β链可变(V)区基因的使用情况。通过使用灵敏的核糖核酸酶保护试验来测量T细胞受体mRNA水平,我们发现在来自三种同源H-2不同的小鼠品系的T细胞群体中,以及在相互排斥的Ly2 + L3T4-和Ly2- L3T4 + T细胞亚群之间,三种Vα基因和三种Vβ基因的使用情况没有显著差异。这些结果表明,主要组织相容性复合体限制不能用不重叠的Vα或Vβ基因库的差异使用来解释。相比之下,在用特定同种异体抗原激活选择的T细胞群体中,V基因使用情况出现了显著但不可预测的差异。