Fox B S, Quill H, Carlson L, Schwartz R H
J Immunol. 1987 May 15;138(10):3367-74.
Planar lipid membranes containing the purified Ia molecule E beta k:E alpha k can present a peptide antigen derived from cytochrome c to the T cell hybridoma 2B4.11. The incorporation of E beta k:E alpha k into planar membranes was linear over a 120-fold range of Ia molecule concentrations, permitting the dependence of the T cell response on the Ia molecule concentration to be examined. As the Ia molecule concentration was increased in the planar membranes, two parameters changed: less antigen was needed to stimulate the T cells, and the plateau response seen at functionally saturating concentrations of antigen increased. The antigen sensitivity was analyzed by plotting the antigen concentration (log2) required to stimulate the release of 10 U of IL 2 from the T cells as a function of the Ia molecule concentration (log2). If the T cell recognized a simple unit of one antigen molecule and one Ia molecule, this plot should have generated a straight line with a slope of -1. Surprisingly, a line with a slope of -2.04 X/divided by 1.12 was observed, suggesting that the T cell might recognize one antigen molecule and two Ia molecules. This complexity, however, resulted from changes in the maximal response achieved at different Ia molecule concentrations. A similar phenomenon was observed when the Ia molecule concentration was decreased in cultures containing splenic antigen-presenting cells (APC) by the addition of an anti-E beta k:E alpha k monoclonal antibody, or the use of [B10.A(4R) X B10.PL]F1APC. The Ia molecule concentration can therefore be limiting for T cell hybridomas in cultures containing normal APC and functionally saturating amounts of antigen. When the planar membrane data were normalized to the maximal response to eliminate the effect of the changing plateau response, the resulting plot generated a line with a slope of -1.17 X/divided by 1.11. These results suggest that the sole stimulatory signal for this T cell hybridoma consisted of a 1:1 ratio of antigen and Ia molecules.
含有纯化的Ia分子Eβk:Eαk的平面脂质膜能够将细胞色素c衍生的肽抗原呈递给T细胞杂交瘤2B4.11。在120倍的Ia分子浓度范围内,Eβk:Eαk掺入平面膜的过程呈线性,这使得我们能够研究T细胞反应对Ia分子浓度的依赖性。随着平面膜中Ia分子浓度的增加,有两个参数发生了变化:刺激T细胞所需的抗原减少,并且在抗原功能饱和浓度下观察到的平台期反应增加。通过绘制刺激T细胞释放10 U白细胞介素2所需的抗原浓度(log2)作为Ia分子浓度(log2)的函数来分析抗原敏感性。如果T细胞识别一个抗原分子和一个Ia分子的简单单位,那么这个图应该会产生一条斜率为-1的直线。令人惊讶的是,观察到的直线斜率为-2.04÷1.12,这表明T细胞可能识别一个抗原分子和两个Ia分子。然而,这种复杂性是由不同Ia分子浓度下达到的最大反应变化导致的。当通过添加抗Eβk:Eαk单克隆抗体或使用[B10.A(4R)×B10.PL]F1抗原呈递细胞(APC)来降低含有脾细胞APC的培养物中的Ia分子浓度时,也观察到了类似的现象。因此,在含有正常APC和功能饱和量抗原的培养物中,Ia分子浓度可能会限制T细胞杂交瘤。当将平面膜数据归一化为最大反应以消除平台期反应变化的影响时,得到的图产生了一条斜率为-1.17÷1.11的直线。这些结果表明,这个T细胞杂交瘤的唯一刺激信号由抗原和Ia分子的1:1比例组成。