Lgr5 homologues associate with Wnt receptors and mediate R-spondin signalling
By W. de Lau, Nick Barker, T. Low, Bonil Koo, Vivian S. W. Li, Hans Teunissen, P. Kujala, A. Haegebarth, P. Peters, M. van de Wetering and 9 more. Nature, 2011
1,270 citations recorded by the source corpus.
Subfields: Hepatology, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/c52ba19f188c743714ae823112fa10cedd9338e4
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In Hepatology
In Molecular Biology
Citations in the corpus
- Metabolic regulation of hematopoietic stem cells in the hypoxic niche. (2011, background): “Cell Stem Cell 9 cells in the murine intestinal and gastric epithelia, which are marked by expression of a leucine-rich G protein-coupled receptor (Lgr5) that functions as an R-spondin receptor (de Lau et al., 2011), divide every 24 hr (Snippert and Clevers, 2011).”
- Functional repair of CFTR by CRISPR/Cas9 in intestinal stem cell organoids of cystic fibrosis patients. (2013, background): “A crucial ingredient is the Wnt agonistic R-spondin1, a ligand of Lgr5 (Carmon et al., 2011; de Lau et al., 2011).”
- Wnt signaling in development and tissue homeostasis (2018, background): “However, the precise role of LGR5 and its homologs LGR4/LGR6 remained controversial until the discovery that they function as receptors for four R-spondin secreted proteins, RSPO1-RSPO4 (Carmon et al., 2011; de Lau et al., 2011; Glinka et al., 2011).”
- Identification of multipotent luminal progenitor cells in human prostate organoid cultures (2014, background): “These cultures can be initiated from single Lgr5+ stem cells and are based on the addition of the Lgr4/5 ligand R-spondin1, a potent Wnt pathway agonist (Binnerts et al., 2007; Carmon et al., 2011; de Lau et al., 2011).”
- Prospective derivation of a Living Organoid Biobank of colorectal cancer patients (2015, positive): “R-spondin-1 is the ligand for Lgr5 (Carmon et al., 2011; de Lau et al., 2011).”
- Wnt/ b -Catenin Signaling, Disease, and Emerging Therapeutic Modalities (2017, background): “The Lgr proteins bind R-spondins through their N-terminal ectodomain and do not appear to utilize G-proteins (Carmon et al., 2011; de Lau et al., 2011).”