Madrenas J, Wange R L, Wang J L, Isakov N, Samelson L E, Germain R N
Lymphocyte Biology Section, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892.
Science. 1995 Jan 27;267(5197):515-8. doi: 10.1126/science.7824949.
Small changes in the peptide-major histocompatibility complex (MHC) molecule ligands recognized by antigen-specific T cell receptors (TCRs) can convert fully activating complexes into partially activating or even inhibitory ones. This study examined early TCR-dependent signals induced by such partial agonists or antagonists. In contrast to typical agonist ligands, both an antagonist and several partial agonists stimulated a distinct pattern of zeta chain phosphorylation and failed to activate associated ZAP-70 kinase. These results identify a specific step in the early tyrosine phosphorylation cascade that is altered after TCR engagement with modified peptide-MHC molecule complexes. This finding may explain the different biological responses to TCR occupancy by these variant ligands.
抗原特异性T细胞受体(TCR)识别的肽 - 主要组织相容性复合体(MHC)分子配体的微小变化可将完全激活的复合体转变为部分激活甚至抑制性复合体。本研究检测了此类部分激动剂或拮抗剂诱导的早期TCR依赖性信号。与典型的激动剂配体不同,拮抗剂和几种部分激动剂均刺激了ζ链磷酸化的独特模式,且未能激活相关的ZAP - 70激酶。这些结果确定了早期酪氨酸磷酸化级联反应中的一个特定步骤,该步骤在TCR与修饰的肽 - MHC分子复合体结合后发生改变。这一发现可能解释了这些变体配体对TCR占据的不同生物学反应。