Chang M D, Jaureguiberry B, Garrido E, Diamond B
Department of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY 10461.
Proc Natl Acad Sci U S A. 1990 Apr;87(7):2501-5. doi: 10.1073/pnas.87.7.2501.
Little is known about the molecular basis for activation of suppressor T cells. In this report we describe two macrophage cell lines, BAC1.2.SC8 and its variant progeny B26, that differ in their ability to activate suppressor T cells. The SC8 line is derived from a (BALB/c x A.CA)F1 (H-2d/f) mouse and is haploid with respect to I-Ed. It is capable of activating I-Ed-restricted helper T cells as well as poly-(Glu50Tyr50)-specific I-Ed-restricted suppressor cells. The B26 variant can activate H-2d-restricted helper T cells but activates H-2k-restricted suppressor cells. The I-Ed molecules of SC8 and of B26 have identical amino acid sequences. This suggests that suppressor T cells either recognize posttranslational modifications of the I-E molecule or that there is another accessory molecule that helps determine the major histocompatibility complex restriction in the activation of suppressor T cells.
关于抑制性T细胞激活的分子基础,人们了解甚少。在本报告中,我们描述了两种巨噬细胞系,BAC1.2.SC8及其变异后代B26,它们在激活抑制性T细胞的能力上存在差异。SC8细胞系源自(BALB/c×A.CA)F1(H-2d/f)小鼠,在I-Ed方面是单倍体。它能够激活I-Ed限制性辅助性T细胞以及聚(谷氨酸50酪氨酸50)特异性I-Ed限制性抑制性细胞。B26变异体能够激活H-2d限制性辅助性T细胞,但激活H-2k限制性抑制性细胞。SC8和B26的I-Ed分子具有相同的氨基酸序列。这表明抑制性T细胞要么识别I-E分子的翻译后修饰,要么存在另一种辅助分子,有助于确定抑制性T细胞激活过程中的主要组织相容性复合体限制。