Knall C, Ingold A, Potter T A
Division of Basic Immunology, National Jewish Center for Immunology and Respiratory Medicine, Denver, CO 80206.
Mol Immunol. 1994 Aug;31(12):875-83. doi: 10.1016/0161-5890(94)90007-8.
Substitution in the alpha 3 domain of class I molecules can ablate the recognition of target cells by CD8 dependent cytotoxic T lymphocytes. This effect has been attributed to a destruction of the CD8 alpha binding site on the class I molecule, a hypothesis which is consistent with results obtained in conjugate binding assays. To assess the relative contribution to CTL activation of CD8 functioning as either a coreceptor or an accessory molecule, we have compared the ability of H-2Kb ovalbumin reactive CTL to lyse M12.C3 or T2 cells transfected with an H-2Kb gene encoding a wild type or mutant (CD8 nonbinding) alpha 3 domain. To establish that the substitution in the alpha 3 domain does not alter the ability of the H-2Kb molecule to bind the antigenic peptide, we have compared the binding of the ovalbumin derived H-2Kb restricted peptide (SIINFEKL) to T2 cells expressing either the CD8 binding or the CD8 nonbinding form of H-2Kb. This peptide conjugated with FITC bound equally well to T2 cells expressing either form of H-2Kb. Upon binding of this peptide, both forms of the H-2Kb molecule underwent the same conformational change as revealed by increases in the expression of particular serological epitopes. Furthermore, inhibition of the binding of the SIINFEKL peptide to both the wild type and mutant H-2Kb was observed following pretreatment of the cells with similar amounts of other H-2Kb restricted peptides derived from Sendai and Vesicular Stomatitis viruses. When the transfected M12 cells were tested for their ability to serve as targets for an anti-H-2Kb ovalbumin CTL clone, cells expressing the mutant H-2Kb molecule required the addition of 100-fold more exogenous peptide than did cells expressing the wild type molecule in order to obtain significant lysis. These data strengthen the previous hypothesis that CD8 functions much more efficiently as a coreceptor than as an accessory molecule for T cell effector function.
I类分子α3结构域的替换可消除CD8依赖性细胞毒性T淋巴细胞对靶细胞的识别。这种效应被归因于I类分子上CD8α结合位点的破坏,这一假设与在结合测定中获得的结果一致。为了评估CD8作为共受体或辅助分子对CTL激活的相对贡献,我们比较了H-2Kb卵清蛋白反应性CTL裂解转染了编码野生型或突变型(CD8非结合)α3结构域的H-2Kb基因的M12.C3或T2细胞的能力。为了确定α3结构域的替换不会改变H-2Kb分子结合抗原肽的能力,我们比较了卵清蛋白衍生的H-2Kb限制性肽(SIINFEKL)与表达CD8结合型或CD8非结合型H-2Kb的T2细胞的结合情况。这种与FITC偶联的肽与表达两种形式H-2Kb的T2细胞结合得同样好。在这种肽结合后,两种形式的H-2Kb分子都经历了相同的构象变化,这通过特定血清学表位表达的增加得以揭示。此外,在用来自仙台病毒和水疱性口炎病毒的相似量的其他H-2Kb限制性肽预处理细胞后,观察到SIINFEKL肽与野生型和突变型H-2Kb的结合均受到抑制。当测试转染的M12细胞作为抗H-2Kb卵清蛋白CTL克隆的靶细胞的能力时,表达突变型H-2Kb分子的细胞比表达野生型分子的细胞需要添加多100倍的外源性肽才能获得显著的裂解。这些数据强化了先前的假设,即对于T细胞效应功能,CD8作为共受体比作为辅助分子的功能效率要高得多。