Sakata-Sogawa Kumiko, Tokunaga Makio
RIKEN Research Center for Allergy and Immunology.
Nihon Rinsho. 2007 Feb;65(2):242-6.
T cell receptors (TCR) are activated by a specific antigen and interact with other signaling molecules, such as kinases and adaptors. Aiming at analyzing precisely the dynamic process of T cell signaling, we used a combined system of a planar bilayer and TIRF microscopy. This system allowed us to observe the T cell activation process from the initial cell-bilayer contact (time 0). Our observation revealed that microclusters with TCR were generated at the initial contact to gather into central supramolecular cluster, the immunological synapse, which was believed to be responsible for T cell receptor signaling. Furthermore the microclusters were generated continuously at the periphery even at the sustained state and they migrated toward the central cluster. These results suggested the important role of microclusters in T cell activation.
T细胞受体(TCR)被特定抗原激活,并与其他信号分子相互作用,如激酶和衔接蛋白。为了精确分析T细胞信号传导的动态过程,我们使用了平面双层和全内反射荧光显微镜(TIRF显微镜)的组合系统。该系统使我们能够从最初的细胞 - 双层接触(时间0)开始观察T细胞激活过程。我们的观察结果显示,与TCR相关的微簇在最初接触时产生,并聚集形成中央超分子簇,即免疫突触,据信其负责T细胞受体信号传导。此外,即使在持续状态下,微簇仍在外围持续产生,并向中央簇迁移。这些结果表明微簇在T细胞激活中起重要作用。