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倒带DISC。

Rewinding the DISC.

作者信息

Chaigne-Delalande Benjamin, Moreau Jean-François, Legembre Patrick

机构信息

Université de Bordeaux-2, Bordeaux, France.

出版信息

Arch Immunol Ther Exp (Warsz). 2008 Jan-Feb;56(1):9-14. doi: 10.1007/s00005-008-0002-9. Epub 2008 Feb 5.

Abstract

Fas (CD95/APO-1) belongs to the tumor necrosis factor receptor family and its signaling pathway has been extensively studied over the past 15 years. Blockade of the Fas-mediated apoptotic signal leads to abusive lymphoproliferation, auto-immunity, and an increased risk of developing lymphoma and leukemia. Fas engagement drives the formation of a complex termed DISC (death-inducing signaling complex), which contains the adaptor molecule Fas-associated protein, two members of the caspase family caspase-8 and -10, and a pseudo-caspase termed c-FLIP. According to different authors, DISC formation relies either on the redistribution of Fas into the lipid rafts or the recruitment of the actin cytoskeleton and receptor endocytosis or the production of ceramide. However, the accurate molecular ordering upstream from the formation of DISC remains very puzzling and is highly debated. Herein we review some of the factors that would potentially facilitate or limit the formation of the DISC.

摘要

Fas(CD95/APO-1)属于肿瘤坏死因子受体家族,在过去15年中其信号通路受到了广泛研究。阻断Fas介导的凋亡信号会导致过度的淋巴细胞增殖、自身免疫以及患淋巴瘤和白血病风险增加。Fas的结合驱动了一种名为死亡诱导信号复合物(DISC)的复合物形成,该复合物包含衔接分子Fas相关蛋白、半胱天冬酶家族的两个成员半胱天冬酶-8和-10,以及一个名为c-FLIP的假半胱天冬酶。根据不同作者的观点,DISC的形成要么依赖于Fas重新分布到脂筏中,要么依赖于肌动蛋白细胞骨架的募集、受体的内吞作用或者神经酰胺的产生。然而,在DISC形成上游的精确分子排序仍然非常令人困惑且存在激烈争论。在此我们综述一些可能促进或限制DISC形成的因素。

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