Lo Wan-Lin, Felix Nathan J, Walters James J, Rohrs Henry, Gross Michael L, Allen Paul M
Department of Immunology and Pathology, Washington University School of Medicine, St. Louis, Missouri, USA.
Nat Immunol. 2009 Nov;10(11):1155-61. doi: 10.1038/ni.1796. Epub 2009 Oct 4.
Although CD4(+) and CD8(+) T cells differ in the strength of their positively selecting signal, endogenous positively selecting ligands have been identified only for major histocompatibility complex (MHC) class I-restricted T cell antigen receptors (TCRs). Here we screened for ligands able to positively select MHC class II-restricted TCRs using thymocytes from four I-E(k)-restricted TCR-transgenic mice and a large panel of self peptides. One peptide, gp250, induced positive selection of AND CD4(+) T cells, had no homology with the AND TCR agonist ligand and was recognized with a high degree of specificity. The gp250 peptide acted as a coagonist to initiate the activation and enhance the survival of peripheral AND CD4(+) T cells. Thus, positively selecting ligands are critical in thymocyte development and in the activation and maintenance of peripheral T cells.
尽管CD4(+)和CD8(+) T细胞在其阳性选择信号的强度上有所不同,但仅针对主要组织相容性复合体(MHC)I类限制性T细胞抗原受体(TCR)鉴定出了内源性阳性选择配体。在这里,我们使用来自四只I-E(k)限制性TCR转基因小鼠的胸腺细胞和大量自身肽,筛选能够阳性选择MHC II类限制性TCR的配体。一种肽,gp250,诱导了AND CD4(+) T细胞的阳性选择,与AND TCR激动剂配体没有同源性,并且具有高度特异性的识别。gp250肽作为共激动剂启动外周AND CD4(+) T细胞的活化并增强其存活。因此,阳性选择配体在胸腺细胞发育以及外周T细胞的活化和维持中至关重要。