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改变的T细胞受体配体触发早期T细胞信号的一个子集。

Altered T cell receptor ligands trigger a subset of early T cell signals.

作者信息

Rabinowitz J D, Beeson C, Wülfing C, Tate K, Allen P M, Davis M M, McConnell H M

机构信息

Department of Chemistry, Howard Hughes Medical Institute, Stanford University, California 94305, USA.

出版信息

Immunity. 1996 Aug;5(2):125-35. doi: 10.1016/s1074-7613(00)80489-6.

Abstract

TCR ligands are complexes of peptides and MHC proteins on the surfaces of APCs. Some of these ligands cause T cell proliferation (agonists), while others block it (antagonists). We compared the acid release, calcium flux, and proliferation response of helper T cells to a variety of ligands. We found that all agonist ligands but not most antagonist ligands trigger acid release, a general indicator of early cellular activation. Only a subset of ligands triggering acid release cause sustained calcium flux, and only a subset of these ligands cause T cell proliferation. Antagonist ligands and anti-CD4 antibodies both effectively block T cell proliferation. However, significantly greater antagonist ligand or antibody concentrations are required to block acid release and initial calcium influx. These data demonstrate a hierarchy of early T cell signaling steps and show that altered TCR ligands can initiate some steps while blocking the completion of others.

摘要

TCR配体是抗原呈递细胞(APC)表面肽与MHC蛋白的复合物。其中一些配体可引起T细胞增殖(激动剂),而其他配体则会阻断T细胞增殖(拮抗剂)。我们比较了辅助性T细胞对多种配体的酸释放、钙流和增殖反应。我们发现,所有激动剂配体而非大多数拮抗剂配体都会引发酸释放,这是早期细胞活化的一个通用指标。只有一部分引发酸释放的配体可导致持续的钙流,而只有这些配体中的一部分会引起T细胞增殖。拮抗剂配体和抗CD4抗体均能有效阻断T细胞增殖。然而,需要显著更高浓度的拮抗剂配体或抗体才能阻断酸释放和初始钙内流。这些数据证明了早期T细胞信号传导步骤的层次结构,并表明改变的TCR配体可以启动某些步骤,同时阻断其他步骤的完成。

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