Bertho Nicolas, Cerny Jan, Kim You-Me, Fiebiger Edda, Ploegh Hidde, Boes Marianne
Department of Pathology, Harvard Medical School, Boston, MA 02115, USA.
J Immunol. 2003 Dec 1;171(11):5689-96. doi: 10.4049/jimmunol.171.11.5689.
Activation of naive CD4 T cells by dendritic cells requires the sequential interaction of many TCR molecules with peptide-class II complexes of the appropriate specificity. Such interaction results in morphological transformation of class II MHC-containing endosomal compartments. In this study, we analyze the requirements for long tubular endosomal structures that polarize toward T cell contact sites using dendritic cells from I-A(b) class II -enhanced green fluorescent protein knock-in mice and I-A(b)-restricted CD4 T cells specific for OVA. Clustering of membrane proteins and ligation of T cell adhesion molecules LFA-1 and CD2 are involved in induction of endosomal tubulation. Activation of T cells increases their ability to induce class II-enhanced green fluorescent protein-positive tubules in dendritic cells, in part through up-regulation of CD40 ligand. Remarkably, and in stark contrast with the result obtained with dendritic cells loaded with intact OVA, OVA peptide added to dendritic cells failed to evoke T cell-polarized endosomal tubulation even though both conditions allowed T cell stimulation. These results suggest the existence of microdomains on the membrane of dendritic cells that allow Ag-specific T cells to evoke tubulation in the dendritic cell.
树突状细胞激活初始CD4 T细胞需要许多TCR分子与具有适当特异性的肽 - II类复合物依次相互作用。这种相互作用导致含II类MHC的内体区室发生形态转变。在本研究中,我们使用来自I - A(b) 类II - 增强型绿色荧光蛋白敲入小鼠的树突状细胞和对OVA特异的I - A(b) 限制性CD4 T细胞,分析了朝向T细胞接触位点极化的长管状内体结构的需求。膜蛋白的聚集以及T细胞黏附分子LFA - 1和CD2的连接参与内体微管形成的诱导。T细胞的激活增加了它们在树突状细胞中诱导II类增强型绿色荧光蛋白阳性微管的能力,部分是通过上调CD40配体实现的。值得注意的是,与加载完整OVA的树突状细胞所得到的结果形成鲜明对比,添加到树突状细胞的OVA肽未能引发T细胞极化的内体微管形成,尽管这两种情况都能刺激T细胞。这些结果表明树突状细胞膜上存在微结构域,使得抗原特异性T细胞能够在树突状细胞中引发微管形成。