Three is better than one: Pre-ligand receptor assembly in the regulation of TNF receptor signaling

被引:142
作者
Chan, Francis Ka-Ming [1 ]
机构
[1] Univ Massachusetts, Sch Med, Dept Pathol, Immunol & Virol Program, Worcester, MA 01655 USA
关键词
pre-ligand assembly domain; PLAD; TNF; TRAIL; apoptosis;
D O I
10.1016/j.cyto.2007.03.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The tumor necrosis factor (TNF) family of cytokines and their receptors regulates many areas of metazoan biology. Specifically, this cytolcine-receptor family plays crucial roles in regulating myriad aspects of immune development and functions. Disruption of ligandreceptor interaction or downstream signal transduction components in the TNF family often leads to pathological conditions. Historically, members of the TNF receptor family (TNFRs) were thought to exist as monomeric receptor chains prior to stimulation. Binding of the trimeric ligand then induces the trimerization of the receptors and activation of downstream signaling. However, recent evidence indicates that many TNFRs exist as pre-assembled oligomers on the cell surface. Pre-ligand assembly of TNFR oligomers is mediated by the pre-ligand assembly domain (PLAD), which resides within the membrane distal cysteine-rich domain of the receptors. Growing evidence indicates that PLAD-mediated receptor association regulates cellular responses to TNF-like cytokines, especially in cells of the immune system. Thus, targeting pre-ligand assembly may offer new possibilities for therapeutic intervention in different pathological conditions involving TNF-like cytokines. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:101 / 107
页数:7
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