Rich S S, Rich R R
J Exp Med. 1976 Nov 2;144(5):1214-26. doi: 10.1084/jem.144.5.1214.
Suppression of the mixed lymphocyte reaction (MLR) by a soluble factor produced by alloantigen-activated spleen cells requires genetic homology between the factor-producing cells and responder cells in MLR. The ability of lymphocytes used as MLR responder cells to adsorb MLR suppressor factor was tested to investigate the expression of a receptor structure for suppressor molecules. Normal spleen or thymus cells had no effect on suppressor activity. Concanavalin A (Con A)-activated thymocytes, however, effectively removed suppressor activity, suggesting that the receptor is expressed only after activation and is not present or not functional on resting cells. Significantly neither phytohemagglutinin- nor lipopolysaccharide-activated lymphoid cells absorbed the factor. Furthermore, only Con A-activated thymocytes demonstrating genetic homology with the cell producing suppressor factor for H-2 regions to the right of I-E were effective absorbants. Alloantigen-stimulated spleen cells syngeneic to the suppressor cell also removed suppressor activity. These data support an hypothesis that subsequent to stimulation in MLR, T lymphocytes express a receptor, either through synthesis or alteration of an existing molecular structure, which then provides the appropriate site for interaction with suppressor molecules.
同种异体抗原激活的脾细胞产生的可溶性因子对混合淋巴细胞反应(MLR)的抑制作用,要求在MLR中产生因子的细胞与应答细胞之间存在基因同源性。测试用作MLR应答细胞的淋巴细胞吸附MLR抑制因子的能力,以研究抑制分子受体结构的表达。正常脾细胞或胸腺细胞对抑制活性无影响。然而,伴刀豆球蛋白A(Con A)激活的胸腺细胞能有效去除抑制活性,这表明该受体仅在激活后表达,在静息细胞上不存在或无功能。值得注意的是,植物血凝素或脂多糖激活的淋巴细胞均不能吸附该因子。此外,只有与产生H-2区域I-E右侧抑制因子的细胞具有基因同源性的Con A激活的胸腺细胞才是有效的吸附剂。与抑制细胞同基因的同种异体抗原刺激的脾细胞也能去除抑制活性。这些数据支持这样一种假说,即在MLR中受到刺激后,T淋巴细胞通过合成或改变现有分子结构来表达一种受体,该受体随后为与抑制分子相互作用提供合适的位点。