Section Dynamique Moléculaire des Interactions Lymphocytaires, Institut National de la Santé et de la Recherche Médicale, Unité Mixte de Recherche 1043, Centre de Physiopathologie de Toulouse Purpan, 31024 Toulouse, France.
Proc Natl Acad Sci U S A. 2013 Apr 9;110(15):6073-8. doi: 10.1073/pnas.1218640110. Epub 2013 Mar 27.
It is presently assumed that lethal hit delivery by cytotoxic T lymphocytes (CTLs) is mechanistically linked to centrosome polarization toward target cells, leading to dedicated release of lytic granules within a confined secretory domain. Here we provide three lines of evidence showing that this mechanism might not apply as a general paradigm for lethal hit delivery. First, in CTLs stimulated with immobilized peptide-MHC complexes, lytic granules and microtubule organizing center localization into synaptic areas are spatio-temporally dissociated, as detected by total internal reflection fluorescence microscopy. Second, in many CTL/target cell conjugates, lytic granule secretion precedes microtubule polarization and can be detected during the first minute after cell-cell contact. Third, inhibition of microtubule organizing center and centrosome polarization impairs neither lytic granule release at the CTL synapse nor killing efficiency. Our results broaden current views of CTL biology by revealing an extremely rapid step of lytic granule secretion and by showing that microtubule organizing center polarization is dispensable for efficient lethal hit delivery.
目前认为,细胞毒性 T 淋巴细胞 (CTL) 的致死性打击传递与中心体向靶细胞的极化在机制上相关联,导致在一个受限的分泌域内专门释放裂解颗粒。在这里,我们提供了三条证据,表明这种机制可能不适用于致死性打击传递的一般范例。首先,在用固定化肽-MHC 复合物刺激的 CTL 中,通过全内反射荧光显微镜检测到裂解颗粒和微管组织中心定位到突触区在时空上是分离的。其次,在许多 CTL/靶细胞共轭物中,裂解颗粒的分泌先于微管极化,并且可以在细胞-细胞接触后的第一分钟内检测到。第三,微管组织中心和中心体极化的抑制既不影响 CTL 突触处的裂解颗粒释放,也不影响杀伤效率。我们的结果通过揭示裂解颗粒分泌的极其快速步骤,并表明微管组织中心极化对于有效的致死性打击传递是可有可无的,从而拓宽了当前对 CTL 生物学的认识。