Departamento de Imunologia, Instituto de Ciências Biomédicas, Universidade de São Paulo, São Paulo, Brazil.
Cell Mol Life Sci. 2010 May;67(10):1631-42. doi: 10.1007/s00018-010-0289-7. Epub 2010 Mar 20.
The death receptor ligands are involved in many physiological and pathological processes involving triggering of apoptosis, inflammation, proliferation, and activation. The expression of these molecules is reported to be tightly regulated at the transcriptional level. However, over the last few years, an increasing number of data demonstrated that the control of transcription is only one of the mechanisms that manage the expression of the death receptor ligands. Thus, this review is focused on posttranslational regulation of the three main members of this family, namely FasL, TNF-alpha, and TRAIL. We discuss here the importance of distribution, storage, and degranulation of these molecules, as well as their shedding by proteases on the control of death receptor ligands expression and activity.
死亡受体配体参与了许多涉及触发细胞凋亡、炎症、增殖和激活的生理和病理过程。据报道,这些分子的表达在转录水平受到严格调控。然而,在过去的几年中,越来越多的研究数据表明,转录的控制只是管理死亡受体配体表达的机制之一。因此,本综述集中讨论了这个家族的三个主要成员(即 FasL、TNF-α和 TRAIL)的翻译后调控。我们在这里讨论了这些分子的分布、储存和脱颗粒以及蛋白酶对其脱落对死亡受体配体表达和活性的控制的重要性。