Brocker T
Basel Institute for Immunology, Switzerland.
J Exp Med. 1997 Oct 20;186(8):1223-32. doi: 10.1084/jem.186.8.1223.
Thymic T cell development is controlled by T cell receptor (TCR)-major histocompatibility complex (MHC) interactions, whereas a further dependence of peripheral mature T cells on TCR-MHC contact has not been described so far. To study this question, CD4 T cell survival was surveyed in mice lacking MHC class II expression and in mice expressing MHC class II exclusively on dendritic cells. Since neither of these mice positively select CD4 T cells in the thymus, they were grafted with MHC class II-positive embryonic thymic tissue, which had been depleted of bone marrow derived cells. Although the thymus grafts in both hosts were repopulated with host origin thymocytes of identical phenotype and numbers, an accumulation of CD4+ T cells in peripheral lymphoid organs could only be observed in mice expressing MHC class II on dendritic cells, but not in mice that were completely MHC class II deficient. As assessed by histology, the accumulating peripheral CD4 T cells were found to be in close contact with MHC class II+ dendritic cells, suggesting that CD4 T cells need peripheral MHC class II expression for survival and that class II+ dendritic cells might play an important role for the longevity of CD4 T cells.
胸腺T细胞的发育受T细胞受体(TCR)-主要组织相容性复合体(MHC)相互作用的控制,而外周成熟T细胞对TCR-MHC接触的进一步依赖性目前尚未见报道。为研究这一问题,我们检测了缺乏MHC II类分子表达的小鼠以及仅在树突状细胞上表达MHC II类分子的小鼠中CD4 T细胞的存活情况。由于这两种小鼠在胸腺中均不能阳性选择CD4 T细胞,因此将它们移植了已去除骨髓来源细胞的MHC II类分子阳性的胚胎胸腺组织。尽管两个宿主中的胸腺移植物均被相同表型和数量的宿主来源胸腺细胞重新填充,但仅在树突状细胞上表达MHC II类分子的小鼠外周淋巴器官中可观察到CD4 + T细胞的积累,而在完全缺乏MHC II类分子的小鼠中则未观察到。通过组织学评估发现,积累的外周CD4 T细胞与MHC II +树突状细胞紧密接触,这表明CD4 T细胞需要外周MHC II类分子的表达来维持存活,并且II类+树突状细胞可能对CD4 T细胞的长寿起重要作用。