Division of Cell and Molecular Biology, Imperial College London, South Kensington, London SW7 2AZ, UK.
Curr Top Microbiol Immunol. 2010;340:63-79. doi: 10.1007/978-3-642-03858-7_4.
Cell contact-dependent inhibition and regulation of immune responses play an essential role in balancing the need for rapid and efficient responses to a wide variety of pathological challenges, while at the same time maintaining self-tolerance. Much attention has been given to immune synapses that lead to the activation of, for example, cell-mediated cytotoxicity, and here we compare the supramolecular dynamics of synapses that lead to inhibition or regulatory functions. We focus on natural killer cells where such different synapses have been best studied. An emergent principle is that inhibition or regulatory responses are commonly achieved by selective recruitment of signalling proteins to the synapse and exclusion of membrane-proximal intracellular proteins needed for activation. We also discuss evidence that an inhibitory synapse triggers or maintains effector cells in a migratory configuration, which serves to break the synapse before the steps needed for effector cell activation can be completed. This model implies that the concept of kinetic-proofreading, previously used to describe activation of individual T-cell receptors, can also apply in determining the outcome of intercellular conjugation.
细胞接触依赖性抑制和免疫反应调节在平衡对各种病理挑战的快速有效反应的需求方面发挥着重要作用,同时保持自身耐受。人们非常关注导致例如细胞介导的细胞毒性的免疫突触,在这里我们比较了导致抑制或调节功能的突触的超分子动力学。我们专注于自然杀伤细胞,在这些细胞中已经对这种不同的突触进行了最好的研究。一个新出现的原则是,抑制或调节反应通常通过选择性招募信号蛋白到突触并排除激活所需的膜近端细胞内蛋白来实现。我们还讨论了证据表明,抑制性突触触发或维持效应细胞处于迁移状态,这有助于在完成效应细胞激活所需的步骤之前打破突触。该模型意味着先前用于描述单个 T 细胞受体激活的动力学校验概念也可适用于确定细胞间连接的结果。