Finetti Francesca, Cassioli Chiara, Baldari Cosima T
Department of Life Sciences, University of Siena, via A. Moro 2, Siena, 53100, Italy.
F1000Res. 2017 Oct 24;6:1880. doi: 10.12688/f1000research.11944.1. eCollection 2017.
The cell's ability to communicate with the extracellular environment, with other cells, and with itself is a crucial feature of eukaryotic organisms. In the immune system, T lymphocytes assemble a specialized structure upon contact with antigen-presenting cells bearing a peptide-major histocompatibility complex ligand, known as the immunological synapse (IS). The IS has been extensively characterized as a signaling platform essential for T-cell activation. Moreover, emerging evidence identifies the IS as a device for vesicular traffic-mediated cell-to-cell communication as well as an active release site of soluble molecules. Here, we will review recent advances in the role of vesicular trafficking in IS assembly and focused secretion of microvesicles at the synaptic area in naïve T cells and discuss the role of the IS in transcellular communication.
细胞与细胞外环境、其他细胞以及自身进行通讯的能力是真核生物的一个关键特征。在免疫系统中,T淋巴细胞在与携带肽-主要组织相容性复合体配体的抗原呈递细胞接触时会组装一种特殊结构,即免疫突触(IS)。免疫突触已被广泛描述为T细胞激活所必需的信号平台。此外,新出现的证据表明免疫突触是一种通过囊泡运输介导细胞间通讯的装置,也是可溶性分子的主动释放位点。在这里,我们将综述囊泡运输在幼稚T细胞免疫突触组装以及突触区域微泡聚焦分泌中作用的最新进展,并讨论免疫突触在跨细胞通讯中的作用。