Saito Takashi, Yokosuka Tadashi
Laboratory for Cell Signaling, RIKEN Research Center for Allergy and Immunology, 1-7-22 Suehiro-cho, Tsurumi-ku, Yokohama 230-0045, Japan.
Curr Opin Immunol. 2006 Jun;18(3):305-13. doi: 10.1016/j.coi.2006.03.014. Epub 2006 Apr 17.
An immunological synapse (IS) is formed at the interface between antigen-presenting cells and T cells, and is believed to be the structure responsible for antigen recognition and T-cell activation. However, recent imaging analyses reveal that T-cell receptor microclusters (MCs) formed prior to IS are the site for antigen recognition and T-cell activation. MCs are continuously generated at the periphery of the interface, even after IS formation, and induce sustained activation signals. MC formation is not accompanied by lipid-raft clustering. Central supramolecular activation cluster is considered functional in recycling and degradation of T-cell receptors, directional secretion of cytokines and cytolytic granules, generation of sustained signals, or maintenance of the cell-cell conjugation.
免疫突触(IS)形成于抗原呈递细胞与T细胞之间的界面,被认为是负责抗原识别和T细胞激活的结构。然而,最近的成像分析表明,在免疫突触形成之前形成的T细胞受体微簇(MCs)是抗原识别和T细胞激活的位点。即使在免疫突触形成后,微簇仍在界面周边持续产生,并诱导持续的激活信号。微簇的形成不伴有脂筏聚集。中央超分子激活簇被认为在T细胞受体的循环和降解、细胞因子和溶细胞颗粒的定向分泌、持续信号的产生或细胞间结合的维持中发挥作用。