Chies J A, Marodon G, Joret A M, Regnault A, Lembezat M P, Rocha B, Freitas A A
INSERM Unit 345, Necker Institute, Paris, France.
J Immunol. 1995 Nov 1;155(9):4171-8.
We have studied V alpha 2 and J beta usage by V beta 6+CD4+ peripheral T cells isolated from the congenic mice strains BALB/c (Mls-1b) and BALB.D2 (Mls-1a). We found that the TCR beta-chain of V beta 6+CD4+ T cells present in adult Mls-1a mice differed from those in Mls-1b mice; the fraction of V beta 6+CD4+T cells using the J beta 2.7 segment was reduced, while the number of V beta 6+CD4+ T cells using J beta 1.2 was augmented. These results indicate that the CDR3 region of the TCR beta-chain participates in recognition of the Mls superantigen. We also found that in Mls-1a mice an increased fraction of V beta 6+CD4+ T cells expressed the V alpha 2 chain. The study of J beta usage by V beta 6+CD4+V alpha 2+ and V beta 6+CD4+V alpha 2- T cells indicates that both J beta segment and TCR V alpha 2 chain expression confer complementary protection against deletion by Mls-1a superantigen. These results suggest a novel view of Mls-1a-driven selection, where the CDR3 region of the V beta chain modulates superantigen recognition, and the affinity/avidity of the TCR-MHC-superantigen complex determine the fate of the T cell.
我们研究了从同基因小鼠品系BALB/c(Mls-1b)和BALB.D2(Mls-1a)分离出的Vβ6+CD4+外周T细胞的Vα2和Jβ使用情况。我们发现,成年Mls-1a小鼠中存在的Vβ6+CD4+T细胞的TCRβ链与Mls-1b小鼠中的不同;使用Jβ2.7片段的Vβ6+CD4+T细胞比例降低,而使用Jβ1.2的Vβ6+CD4+T细胞数量增加。这些结果表明,TCRβ链的CDR3区域参与了对Mls超抗原的识别。我们还发现,在Mls-1a小鼠中,Vβ6+CD4+T细胞中表达Vα2链的比例增加。对Vβ6+CD4+Vα2+和Vβ6+CD4+Vα2-T细胞的Jβ使用情况研究表明,Jβ片段和TCR Vα2链的表达都赋予了针对Mls-1a超抗原缺失的互补保护。这些结果提示了一种关于Mls-1a驱动选择的新观点,其中Vβ链的CDR3区域调节超抗原识别,而TCR-MHC-超抗原复合物的亲和力/亲合力决定了T细胞的命运。