Vacchio M S, Hodes R J
Experimental Immunology Branch, National Cancer Institute, Bethesda, Maryland 20892.
J Exp Med. 1989 Oct 1;170(4):1335-46. doi: 10.1084/jem.170.4.1335.
Previous reports of TCR V beta usage, studying either expression of a single V beta in a wide panel of strains (6, 7, 10, 12, 13), or expression of multiple V beta s in a very limited strain distribution (14, 15), have identified instances of clonal deletion of potentially autoreactive T cells specific for either self E alpha E beta or minor lymphocyte stimulatory (Mls) antigens. The present study has investigated the range of self antigens that can influence V beta usage by evaluating expression of 16 V beta families in 30 strains of mice. It was found that significant decreases in expression occur in at least 8 of the 16 V beta families and that dominant influences on the T cell V beta repertoire are exerted by expression of Mlsa, Mlsc, and MHC gene products. Decreased expressions of V beta 5, -11, -12, and -16 were influenced by MHC gene products. The patterns of decreased expression seen in intra-MHC recombinant strains and strains of different non-MHC background were distinct for V beta 11, -12, and -16, suggesting that different ligands are involved in the deletion of T cells expressing each of these V beta genes. Mice expressing Mlsa show decreased expression of V beta 9 as well as V beta 6. Mlsc mice lacked V beta 3 expression in those strains where the expressed MHC type was compatible with a strongly stimulatory Mlsc phenotype. V beta 7 was strongly influenced by both MHC and non-MHC products that are not yet identified. These results demonstrate that strain-specific decreases of mRNA expression occur in a major portion of the TCR repertoire. Self antigens including Mlsa, Mlsc, and E alpha E beta, as well as additional MHC and non-MHC products, appear to induce these decreases in expression in the process of eliminating self-reactive T cells from the mature T cell pool.
先前有关TCR Vβ使用情况的报告,要么研究了多种品系中单个Vβ的表达(6、7、10、12、13),要么研究了非常有限的品系分布中多个Vβ的表达(14、15),这些报告已经确定了针对自身EαEβ或次要淋巴细胞刺激(Mls)抗原的潜在自身反应性T细胞发生克隆性缺失的实例。本研究通过评估30种小鼠品系中16个Vβ家族的表达,调查了能够影响Vβ使用情况的自身抗原范围。研究发现,16个Vβ家族中至少有8个家族的表达出现显著下降,并且Mlsa、Mlsc和MHC基因产物的表达对T细胞Vβ库有主要影响。Vβ5、-11、-12和-16的表达下降受MHC基因产物影响。在MHC内重组品系和不同非MHC背景的品系中,Vβ11、-12和-16的表达下降模式不同,这表明不同的配体参与了表达这些Vβ基因的T细胞的缺失。表达Mlsa的小鼠Vβ9以及Vβ6的表达下降。在那些表达的MHC类型与强刺激Mlsc表型相容的品系中,Mlsc小鼠缺乏Vβ3表达。Vβ7受到尚未确定的MHC和非MHC产物的强烈影响。这些结果表明,TCR库的主要部分出现了品系特异性的mRNA表达下降。包括Mlsa、Mlsc和EαEβ在内的自身抗原,以及其他MHC和非MHC产物,似乎在从成熟T细胞库中消除自身反应性T细胞的过程中诱导了这些表达下降。