Department of Life Sciences, University of Siena, Siena, Italy.
Front Immunol. 2022 Apr 20;13:883010. doi: 10.3389/fimmu.2022.883010. eCollection 2022.
Cytotoxic T cells (CTLs) are the main cellular mediators of the adaptive immune defenses against intracellular pathogens and malignant cells. Upon recognition of specific antigen on their cellular target, CTLs assemble an immunological synapse where they mobilise their killing machinery that is released into the synaptic cleft to orchestrate the demise of their cell target. The arsenal of CTLs is stored in lysosome-like organelles that undergo exocytosis in response to signals triggered by the T cell antigen receptor following antigen recognition. These organelles include lytic granules carrying a cargo of cytotoxic proteins packed on a proteoglycan scaffold, multivesicular bodies carrying the death receptor ligand FasL, and the recently discovered supramolecular attack particles that carry a core of cytotoxic proteins encased in a non-membranous glycoprotein shell. Here we will briefly review the main features of these killing entities and discuss their interrelationship and interplay in CTL-mediated killing.
细胞毒性 T 细胞 (CTL) 是适应性免疫防御针对细胞内病原体和恶性细胞的主要细胞介质。在识别其细胞靶标上的特定抗原后,CTL 组装免疫突触,在突触小间隙中动员其杀伤机制,以协调其细胞靶标的死亡。CTL 的武器库储存在溶酶体样细胞器中,这些细胞器在 T 细胞抗原受体识别抗原后,通过信号触发进行胞吐作用。这些细胞器包括携带包装在糖蛋白支架上的细胞毒性蛋白货物的溶酶体颗粒、携带死亡受体配体 FasL 的多泡体,以及最近发现的携带包裹在非膜糖蛋白壳中的细胞毒性蛋白核心的超分子攻击颗粒。在这里,我们将简要回顾这些杀伤实体的主要特征,并讨论它们在 CTL 介导的杀伤中的相互关系和相互作用。