The co-receptor Tetraspanin12 directly captures Norrin to promote ligand-specific β-catenin signaling

Wnt/β-catenin signaling directs animal development and tissue renewal in a tightly controlled, cell- and tissue-specific manner. In the mammalian central nervous system, the atypical ligand Norrin controls angiogenesis and maintenance of the blood-brain barrier and blood-retina barrier through the W...

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Main Authors: Elise S Bruguera, Jacob P Mahoney, William I Weis
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2025-01-01
Series:eLife
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Online Access:https://elifesciences.org/articles/96743
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author Elise S Bruguera
Jacob P Mahoney
William I Weis
author_facet Elise S Bruguera
Jacob P Mahoney
William I Weis
author_sort Elise S Bruguera
collection DOAJ
description Wnt/β-catenin signaling directs animal development and tissue renewal in a tightly controlled, cell- and tissue-specific manner. In the mammalian central nervous system, the atypical ligand Norrin controls angiogenesis and maintenance of the blood-brain barrier and blood-retina barrier through the Wnt/β-catenin pathway. Like Wnt, Norrin activates signaling by binding and heterodimerizing the receptors Frizzled (Fzd) and low-density lipoprotein receptor-related protein 5 or 6 (LRP5/6), leading to membrane recruitment of the intracellular transducer Dishevelled (Dvl) and ultimately stabilizing the transcriptional coactivator β-catenin. Unlike Wnt, the cystine knot ligand Norrin only signals through Fzd4 and additionally requires the co-receptor Tetraspanin12 (Tspan12); however, the mechanism underlying Tspan12-mediated signal enhancement is unclear. It has been proposed that Tspan12 integrates into the Norrin-Fzd4 complex to enhance Norrin-Fzd4 affinity or otherwise allosterically modulate Fzd4 signaling. Here, we measure direct, high-affinity binding between purified Norrin and Tspan12 in a lipid environment and use AlphaFold models to interrogate this interaction interface. We find that Tspan12 and Fzd4 can simultaneously bind Norrin and that a pre-formed Tspan12/Fzd4 heterodimer, as well as cells co-expressing Tspan12 and Fzd4, more efficiently capture low concentrations of Norrin than Fzd4 alone. We also show that Tspan12 competes with both heparan sulfate proteoglycans and LRP6 for Norrin binding and that Tspan12 does not impact Fzd4-Dvl affinity in the presence or absence of Norrin. Our findings suggest that Tspan12 does not allosterically enhance Fzd4 binding to Norrin or Dvl, but instead functions to directly capture Norrin upstream of signaling.
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spelling doaj-art-abde58c59b6b4c65a9fb4a9cadf5eb2f2025-08-20T02:51:23ZengeLife Sciences Publications LtdeLife2050-084X2025-01-011310.7554/eLife.96743The co-receptor Tetraspanin12 directly captures Norrin to promote ligand-specific β-catenin signalingElise S Bruguera0https://orcid.org/0000-0003-1983-3013Jacob P Mahoney1William I Weis2https://orcid.org/0000-0002-5583-6150Departments of Molecular & Cellular Physiology and Structural Biology, Stanford University School of Medicine, Stanford, United StatesDepartments of Molecular & Cellular Physiology and Structural Biology, Stanford University School of Medicine, Stanford, United StatesDepartments of Molecular & Cellular Physiology and Structural Biology, Stanford University School of Medicine, Stanford, United StatesWnt/β-catenin signaling directs animal development and tissue renewal in a tightly controlled, cell- and tissue-specific manner. In the mammalian central nervous system, the atypical ligand Norrin controls angiogenesis and maintenance of the blood-brain barrier and blood-retina barrier through the Wnt/β-catenin pathway. Like Wnt, Norrin activates signaling by binding and heterodimerizing the receptors Frizzled (Fzd) and low-density lipoprotein receptor-related protein 5 or 6 (LRP5/6), leading to membrane recruitment of the intracellular transducer Dishevelled (Dvl) and ultimately stabilizing the transcriptional coactivator β-catenin. Unlike Wnt, the cystine knot ligand Norrin only signals through Fzd4 and additionally requires the co-receptor Tetraspanin12 (Tspan12); however, the mechanism underlying Tspan12-mediated signal enhancement is unclear. It has been proposed that Tspan12 integrates into the Norrin-Fzd4 complex to enhance Norrin-Fzd4 affinity or otherwise allosterically modulate Fzd4 signaling. Here, we measure direct, high-affinity binding between purified Norrin and Tspan12 in a lipid environment and use AlphaFold models to interrogate this interaction interface. We find that Tspan12 and Fzd4 can simultaneously bind Norrin and that a pre-formed Tspan12/Fzd4 heterodimer, as well as cells co-expressing Tspan12 and Fzd4, more efficiently capture low concentrations of Norrin than Fzd4 alone. We also show that Tspan12 competes with both heparan sulfate proteoglycans and LRP6 for Norrin binding and that Tspan12 does not impact Fzd4-Dvl affinity in the presence or absence of Norrin. Our findings suggest that Tspan12 does not allosterically enhance Fzd4 binding to Norrin or Dvl, but instead functions to directly capture Norrin upstream of signaling.https://elifesciences.org/articles/96743Wntcell signalingspecificityco-receptornanodiscs
spellingShingle Elise S Bruguera
Jacob P Mahoney
William I Weis
The co-receptor Tetraspanin12 directly captures Norrin to promote ligand-specific β-catenin signaling
eLife
Wnt
cell signaling
specificity
co-receptor
nanodiscs
title The co-receptor Tetraspanin12 directly captures Norrin to promote ligand-specific β-catenin signaling
title_full The co-receptor Tetraspanin12 directly captures Norrin to promote ligand-specific β-catenin signaling
title_fullStr The co-receptor Tetraspanin12 directly captures Norrin to promote ligand-specific β-catenin signaling
title_full_unstemmed The co-receptor Tetraspanin12 directly captures Norrin to promote ligand-specific β-catenin signaling
title_short The co-receptor Tetraspanin12 directly captures Norrin to promote ligand-specific β-catenin signaling
title_sort co receptor tetraspanin12 directly captures norrin to promote ligand specific β catenin signaling
topic Wnt
cell signaling
specificity
co-receptor
nanodiscs
url https://elifesciences.org/articles/96743
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