Death receptor signaling and its function in the immune system.

Stefanie C Fas, Benedikt Fritzsching, Elisabeth Suri-Payer, Peter H Krammer
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引用次数: 79

Abstract

Death receptors belong to the TNF (tumor necrosis factor)/NGF (nerve growth factor) receptor superfamily. Signaling via death receptors plays a distinct role, e.g. in the immune system, where it contributes to regulation of the adaptive immune response in various ways, most notably by triggering activation-induced cell death (AICD) of T cells. Thus, dysregulation of death receptor signaling, either allowing too much or too little apoptosis, can lead to autoimmune disorders and also impacts on tumorigenesis or other diseases. In this chapter we address components, molecular mechanisms and regulation of death receptor signaling with particular focus on CD95 (APO-1, Fas). We discuss the role of death receptor-mediated AICD in regulation of the adaptive immune response against foreign and self antigens in comparison to cytokine deprivation-mediated death by neglect. Finally, the contribution of dysregulated death receptor/ligand systems to autoimmune diseases such as diabetes, multiple sclerosis and Hashimoto's thyroiditis is discussed.

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死亡受体信号及其在免疫系统中的功能。
死亡受体属于肿瘤坏死因子(TNF)/神经生长因子(NGF)受体超家族。通过死亡受体传递的信号发挥着独特的作用,例如在免疫系统中,它以各种方式调节适应性免疫反应,最显著的是通过触发T细胞的激活诱导细胞死亡(AICD)。因此,死亡受体信号的失调,无论是导致过多或过少的细胞凋亡,都可能导致自身免疫性疾病,并影响肿瘤发生或其他疾病。在本章中,我们讨论了死亡受体信号的组成、分子机制和调控,特别关注CD95 (APO-1, Fas)。我们讨论了死亡受体介导的AICD在调节针对外来和自身抗原的适应性免疫应答中的作用,并与细胞因子剥夺介导的忽视死亡进行了比较。最后,本文讨论了死亡受体/配体系统失调对自身免疫性疾病如糖尿病、多发性硬化症和桥本甲状腺炎的影响。
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