Kohyama M, Nanno M, Kawaguchi-Miyashita M, Shimada S, Watanabe M, Hibi T, Kaminogawa S, Ishikawa H
Department of Microbiology, Keio University School of Medicine, Tokyo 160-8582, Japan.
Proc Natl Acad Sci U S A. 1999 Jun 22;96(13):7451-5. doi: 10.1073/pnas.96.13.7451.
We analyzed the cytolytic activity of intraepithelial T cells (IEL) isolated from the small intestines of 2- to 3-month-old mutant mice rendered deficient in different gene(s) in which the number of IEL expressing either T cell receptor (TCR)-alpha beta (alpha beta-IEL) or TCR-gamma delta (gamma delta-IEL) were absent or markedly diminished. When compared with wild-type littermates, cytolytic activity of gamma delta-IEL was sharply attenuated in TCR-beta mutant mice but remained unaltered in TCR-alpha mutant mice in which a minor population of dull TCR-beta+ (betadim)-IEL was also present. Cytolytic activity of gamma delta-IEL was maintained in mice doubly homozygous for beta2-microglobulin and transporter associated with antigen processing 1 gene mutations in which a conspicuous decrease was noted in absolute numbers of alpha beta-IEL. In contrast, both TCR-delta and IL-7 receptor-alpha gene mutations that lead to lack of gamma delta-IEL generation did not affect the development or cytolytic activity of the remaining alpha beta-IEL. The anti-CD3 and anti-TCR-gamma delta mAb-induced IFN-gamma production of gamma delta-IEL showed the same TCR-alpha and TCR-beta mutation-dependent variability. These results indicate that cytolytic and IFN-gamma-producing activities of gamma delta T cells in mouse intestinal epithelium are TCR-beta-chain-dependent.
我们分析了从2至3月龄的突变小鼠小肠中分离出的上皮内T细胞(IEL)的细胞溶解活性,这些小鼠缺失了不同的基因,其中表达T细胞受体(TCR)-αβ(αβ-IEL)或TCR-γδ(γδ-IEL)的IEL数量缺失或显著减少。与野生型同窝小鼠相比,γδ-IEL的细胞溶解活性在TCR-β突变小鼠中急剧减弱,但在也存在少量迟钝的TCR-β+(βdim)-IEL的TCR-α突变小鼠中保持不变。在β2-微球蛋白和与抗原加工相关的转运体1基因双纯合突变的小鼠中,γδ-IEL的细胞溶解活性得以维持,其中αβ-IEL的绝对数量显著减少。相反,导致γδ-IEL生成缺失的TCR-δ和IL-7受体-α基因突变均不影响其余αβ-IEL的发育或细胞溶解活性。抗CD3和抗TCR-γδ单克隆抗体诱导的γδ-IEL的IFN-γ产生表现出相同的TCR-α和TCR-β突变依赖性变异性。这些结果表明,小鼠肠道上皮中γδ T细胞的细胞溶解和IFN-γ产生活性是TCR-β链依赖性的。