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Frizzleds and WNT/beta-catenin signaling - The black box of ligand-receptor selectivity, complex stoichiometry and activation kinetics

机译:毛躁和WNT /β-catenin信号-配体-受体选择性,复杂化学计量和活化动力学的黑匣子

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摘要

The lipoglycoproteins of the mammalian WNT family induce beta-catenin-dependent signaling through interaction with members of the Class Frizzled receptors and LDL receptor-related protein 5/6 (LRP5/6) albeit with unknown selectivity. The 10 mammalian Frizzleds (FZDs) are seven transmembrane (7TM) spanning receptors and have recently been classified as G protein-coupled receptors (GPCRs). This review summarizes the current knowledge about WNT/FZD selectivity and functional selectivity, the role of co-receptors for signal specification, the formation of receptor complexes as well as the kinetics and mechanisms of signal initiation with focus on WNT/beta-catenin signaling. In order to exploit the true therapeutic potential of WNT/FZD signaling to treat human disease, it is clear that substantial progress in the understanding of receptor complex formation and signal specification has to precede a mechanism-based drug design targeting WNT receptors. (C) 2015 Elsevier B.V. All rights reserved
机译:哺乳动物WNT家族的脂蛋白通过与毛躁类受体和LDL受体相关蛋白5/6(LRP5 / 6)的成员相互作用,诱导β-catenin依赖性信号传导,尽管选择性未知。 10个哺乳动物的卷毛(FZD)是七个跨膜(7TM)跨接受体,最近被归类为G蛋白偶联受体(GPCR)。这篇综述总结了有关WNT / FZD选择性和功能选择性的当前知识,共受体在信号规范中的作用,受体复合物的形成以及以WNT /β-catenin信号为重点的信号引发的动力学和机理。为了利用WNT / FZD信号的真正治疗潜力来治疗人类疾病,很明显,在理解受体复合物的形成和信号规范方面的实质性进展必须先于针对WNT受体的基于机制的药物设计。 (C)2015 Elsevier B.V.保留所有权利

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