LGR4 and LGR5 are R-spondin receptors mediating Wnt/b-catenin and Wnt/PCP signalling

نویسندگان

  • Andrei Glinka
  • Christine Dolde
  • Nadine Kirsch
  • Ya-Lin Huang
  • Olga Kazanskaya
  • Dierk Ingelfinger
  • Michael Boutros
  • Cristina-Maria Cruciat
  • Christof Niehrs
چکیده

R-spondins are secreted Wnt signalling agonists, which regulate embryonic patterning and stem cell proliferation, but whose mechanism of action is poorly understood. Here we show that R-spondins bind to the orphan G-protein-coupled receptors LGR4 and LGR5 by their Furin domains. Gainand loss-of-function experiments in mammalian cells and Xenopus embryos indicate that LGR4 and LGR5 promote R-spondin-mediated Wnt/b-catenin and Wnt/PCP signalling. R-spondin-triggered b-catenin signalling requires Clathrin, while Wnt3a-mediated b-catenin signalling requires Caveolin-mediated endocytosis, suggesting that internalization has a mechanistic role in R-spondin signalling.

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LGR4 and LGR5 are R-spondin receptors mediating Wnt/β-catenin and Wnt/PCP signalling.

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تاریخ انتشار 2011