Institute for Clinical Microbiology and Hygiene, University of Regensburg, Franz-Josef-Strauss-Allee 11, Regensburg 93053, Germany.
Int J Mol Sci. 2013 Jul 11;14(7):14475-503. doi: 10.3390/ijms140714475.
Death receptors were initially recognised as potent inducers of apoptotic cell death and soon ambitious attempts were made to exploit selective ignition of controlled cellular suicide as therapeutic strategy in malignant diseases. However, the complexity of death receptor signalling has increased substantially during recent years. Beyond activation of the apoptotic cascade, involvement in a variety of cellular processes including inflammation, proliferation and immune response was recognised. Mechanistically, these findings raised the question how multipurpose receptors can ensure selective activation of a particular pathway. A growing body of evidence points to an elegant spatiotemporal regulation of composition and assembly of the receptor-associated signalling complex. Upon ligand binding, receptor recruitment in specialized membrane compartments, formation of receptor-ligand clusters and internalisation processes constitute key regulatory elements. In this review, we will summarise the current concepts of death receptor trafficking and its implications on receptor-associated signalling events.
死亡受体最初被认为是诱导细胞凋亡的有效因子,随后人们雄心勃勃地试图利用选择性引发受控细胞自杀作为恶性疾病的治疗策略。然而,近年来死亡受体信号转导的复杂性大大增加。除了激活凋亡级联反应外,还涉及包括炎症、增殖和免疫反应在内的多种细胞过程。从机制上讲,这些发现提出了一个问题,即多功能受体如何能够确保特定途径的选择性激活。越来越多的证据表明,受体相关信号复合物的组成和组装受到精细的时空调节。配体结合后,受体在专门的膜隔室中的募集、受体-配体簇的形成和内化过程是关键的调节元件。在这篇综述中,我们将总结死亡受体运输的最新概念及其对受体相关信号事件的影响。