Head inducer Dickkopf-1 is a ligand for Wnt coreceptor LRP6.
By Mikhail V. Semenov, K. Tamai, B. Brott, Michael Kühl, S. Sokol, Xi He. Current Biology, 2001
730 citations recorded by the source corpus.
Subfields: Cell Biology, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/4bc9f3016351ce03199c281c3e87774954e5b09a
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Citations in the corpus
- Sclerostin Mediates Bone Response to Mechanical Unloading Through Antagonizing Wnt/β‐Catenin Signaling (2009, background): “Dkk1 antagonism on Wnt/b-catenin signaling was identified originally through its binding with Lrp6.((35,36)) Sclerostin bound to both Lrp5 and Lrp6, and particularly, it was”
- Mutations in LRP5 or FZD4 underlie the common familial exudative vitreoretinopathy locus on chromosome 11q. (2004, background): “Consistent with this notion, LRP5 has been shown to interact with different Wnt/frizzled complexes (Tamai et al. 2000; Semënov et al. 2001; Kato et al. 2002; Caricasole et al. 2003), although the binding sites have not been determined.”
- LDL receptor-related proteins 5 and 6 in Wnt/β-catenin signaling: Arrows point the way (2004, background): “Dkk1 disrupts the FzLrp5/Lrp6 complex formation induced by Wnt1 in vitro (Semenov et al., 2001), suggesting that Dkk1 inhibits Wnt ignaling by preventing Fz-Lrp5/Lrp6 complex formation.”
- Signalling in neural development: WNTS in the vertebrate nervous system: from patterning to neuronal connectivity (2005, background): “, which prevents the formation of the ternary complex between WNT, FZ and LRP and, consequently, activation of the pathwa”
- Secreted antagonists of the Wnt signalling pathway (2003, background): “However, unlike sFRPs, Dkk-1 prevents activation of the Wnt signalling pathway by binding to LRP5/6 rather than to Wnt proteins (Bafico et al., 2001; Mao, B. et al., 2001; Semenov et al., 2001).”
- The Wnt signaling pathway in development and disease. (2004, background): “It binds to LRP with high affinity (Bafico et al. 2001, Mao et al. 2001a, Semenov et al. 2001) and to another class of transmembrane molecules, the Kremens (Mao & Niehrs 2003, Mao et al. 2002).”
- Canonical Wnt signals are essential for homeostasis of the intestinal epithelium. (2003, background): “…1996; Fodde et al. 2001) as well as adenomatous polyp formation in the mouse intestine (Moser et al. 1990; Fodde et al. 1994; Oshima et al. 1995; Shibata et al. 1997), whereas mutation of Tcf4 leads to the depletion of intestinal proliferative compartments in fetal mice (Korinek et al. 1998).”
- Kremen proteins are Dickkopf receptors that regulate Wnt/β-catenin signalling (2002, background): “Dkk1 has been shown to inhibit Wnt signalling by binding to and antagonizing LRP5/”
- Secreted and transmembrane wnt inhibitors and activators. (2013, background): “2002; Mao and Niehrs 2003), and mutation of the conserved Cys-220 of the colipase fold abolishes the interaction (Semenov et al. 2001).”