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Kremen is required for neural crest induction in Xenopus and promotes LRP6-mediated Wnt signaling.Kremen在非洲爪蟾的神经嵴诱导过程中是必需的,并促进LRP6介导的Wnt信号传导。
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R-spondin1 is a high affinity ligand for LRP6 and induces LRP6 phosphorylation and beta-catenin signaling.R-spondin1是低密度脂蛋白受体相关蛋白6(LRP6)的高亲和力配体,并诱导LRP6磷酸化和β-连环蛋白信号传导。
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Dickkopf-1 is a master regulator of joint remodeling.Dickkopf-1是关节重塑的主要调节因子。
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Function and biological roles of the Dickkopf family of Wnt modulators.Dickkopf家族Wnt调节因子的功能及生物学作用。
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LRP5 mutations linked to high bone mass diseases cause reduced LRP5 binding and inhibition by SOST.与高骨量疾病相关的LRP5突变导致LRP5与sclerostin(SOST)的结合减少以及受其抑制作用减弱。
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DKK1拮抗Wnt信号传导,而不促进LRP6的内化和降解。

DKK1 antagonizes Wnt signaling without promotion of LRP6 internalization and degradation.

作者信息

Semënov Mikhail V, Zhang Xinjun, He Xi

机构信息

F. M. Kirby Neurobiology Center, Children's Hospital Boston and Department of Neurology, Harvard Medical School, 61 Binney Street, Boston, MA 02115, USA.

出版信息

J Biol Chem. 2008 Aug 1;283(31):21427-32. doi: 10.1074/jbc.M800014200. Epub 2008 May 27.

DOI:10.1074/jbc.M800014200
PMID:18505732
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2490777/
Abstract

DKK1 is a secreted protein that antagonizes Wnt signaling and plays essential roles in vertebrate embryogenesis including head induction, skeletal development, and limb patterning. DKK1 is also implicated in osteoporosis, arthritis, and cancer and represents a potential therapeutic target for the treatment of these diseases. DKK1 is a high affinity antagonistic ligand for LRP6, which is a Wnt coreceptor that acts together with the Frizzled serpentine receptor to initiate Wnt signal transduction. Two different models have been proposed to account for the mechanism by which DKK1 antagonizes LRP6 function. One model suggests that DKK1 binding to LRP6 disrupts Wnt-induced Frizzled-LRP6 complex formation, whereas the other model proposes that DKK1 interaction with LRP6 promotes LRP6 internalization and degradation, thereby reducing the cell surface LRP6 level. To clarify the molecular basis of DKK1 action, we examined how DKK1 affects the endogenous LRP6 in several mammalian cell lines including mouse embryonic fibroblasts. Here we show that DKK1 inhibits Wnt signaling but induces neither LRP6 down-regulation from the cell surface nor reduction of total LRP6 protein level and that DKK1 has no effect on the rate of continuous internalization of LRP6 and the half-life (about 4.7 h) of LRP6. We conclude that DKK1 inhibition of LRP6 is independent of LRP6 internalization and degradation.

摘要

DKK1是一种分泌蛋白,它拮抗Wnt信号传导,并在脊椎动物胚胎发育中发挥重要作用,包括头部诱导、骨骼发育和肢体模式形成。DKK1还与骨质疏松症、关节炎和癌症有关,是治疗这些疾病的潜在治疗靶点。DKK1是LRP6的高亲和力拮抗配体,LRP6是一种Wnt共受体,与卷曲蛇形受体共同作用以启动Wnt信号转导。已经提出了两种不同的模型来解释DKK1拮抗LRP6功能的机制。一种模型表明,DKK1与LRP6的结合破坏了Wnt诱导的卷曲-LRP6复合物的形成,而另一种模型则提出,DKK1与LRP6的相互作用促进了LRP6的内化和降解,从而降低了细胞表面LRP6的水平。为了阐明DKK1作用的分子基础,我们研究了DKK1如何影响包括小鼠胚胎成纤维细胞在内的几种哺乳动物细胞系中的内源性LRP6。在这里,我们表明DKK1抑制Wnt信号传导,但既不诱导LRP6从细胞表面下调,也不降低LRP6总蛋白水平,并且DKK1对LRP6的持续内化速率和LRP6的半衰期(约4.7小时)没有影响。我们得出结论,DKK1对LRP6的抑制作用独立于LRP6的内化和降解。