Mesd Is a Universal Inhibitor of Wnt Coreceptors LRP5 and LRP6 and Blocks Wnt/β-Catenin Signaling in Cancer Cells

被引:42
|
作者
Lu, Wenyan [1 ]
Liu, Chia-Chen [2 ,3 ]
Thottassery, Jaideep V. [1 ]
Bu, Guojun [2 ,3 ]
Li, Yonghe [1 ]
机构
[1] So Res Inst, Dept Biochem & Mol Biol, Drug Discovery Div, Birmingham, AL 35255 USA
[2] Washington Univ, Sch Med, Dept Pediat, St Louis, MO 63110 USA
[3] Washington Univ, Sch Med, Dept Physiol & Cell Biol, St Louis, MO 63110 USA
基金
美国国家卫生研究院;
关键词
DENSITY-LIPOPROTEIN RECEPTOR; MAMMARY-GLAND DEVELOPMENT; BETA-CATENIN; LUNG-CANCER; MOLECULAR CHAPERONE; PROSTATE-CANCER; LIGAND-BINDING; FAMILY-MEMBERS; EXPRESSION; PATHWAY;
D O I
10.1021/bi1001486
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
Mesd is a specialized chaperone for low-density lipoprotein receptor-related protein 5 (LRP5) and LRP6. In our previous studies, we found that Mesd binds to mature LRP6 on the cell surface and blocks the binding of Wnt antagonist Dickkopf-1 (Dkk1) to LRP6. Herein, we demonstrate that Mesd also binds to LRP5 with a high affinity and is a universal inhibitor of LRP5 and LRP6 ligands. Mesd not only blocks binding of Writ antagonists Dkk1 and Sclerostin to LRP5 and LRP6 but also inhibits Wnt3A and Rspondin 1-induced Wnt/beta-catenin signaling in LRP5- and LRP6-expressing cells. We also found that Mesd, Dkk1, and Sclerostin compete with one another for binding to LRP5 and LRP6 at the cell surface. More importantly, we demonstrated that Mesd is able to suppress LRP6 phosphorylation and Wnt/beta-catenin signaling in prostate cancer PC-3 cells and inhibits PC-3 cell proliferation. Our results indicate that recombinant Mesd protein is a useful tool for studying Wnt/beta-catenin signaling on the cell surface and has a potential therapeutic role in Wnt-dependent cancers.
引用
收藏
页码:4635 / 4643
页数:9
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