Evidence map›Paper›PMID 30304675›Full record

ArticleCell reports2018

A RECK-WNT7 Receptor-Ligand Interaction Enables Isoform-Specific Regulation of Wnt Bioavailability.

Mario Vallon, Kanako Yuki, Thi D Nguyen, Junlei Chang, Jenny Yuan, Dirk Siepe, Yi Miao, Markus Essler, Makoto Noda, K Christopher Garcia and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed, 1 pooled it
5.8field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

72 citing papers in PubMed, 1 synthesis or guideline pooled it, 125 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Adhesion G protein-coupled receptors.Pharmacological reviews · 2026
    Review
  7. Article
  8. Article
  9. Review
  10. Development of the blood-brain barrier.Development (Cambridge, England) · 2026
    Review
  11. Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Complex G-protein signaling of the adhesion GPCR, ADGRA3.The Journal of biological chemistry · 2025
    Article
  18. Review
  19. Article
  20. Review

12 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 3 countries.

Mario VallonDepartment of Medicine, Division of Hematology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Kanako YukiDepartment of Medicine, Division of Hematology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Thi D NguyenDepartment of Medicine, Division of Hematology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Junlei ChangDepartment of Medicine, Division of Hematology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Jenny YuanDepartment of Medicine, Division of Hematology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Dirk SiepeDepartment of Molecular and Cellular Physiology, Department of Structural Biology, and Howard Hughes Medical Institute, Stanford University School of Medicine, Stanford, CA 94305, USA.
Yi MiaoDepartment of Molecular and Cellular Physiology, Department of Structural Biology, and Howard Hughes Medical Institute, Stanford University School of Medicine, Stanford, CA 94305, USA.
Markus EsslerDepartment of Nuclear Medicine, University Hospital Bonn, 53127 Bonn, Germany.
Makoto NodaDepartment of Molecular Oncology, Kyoto University Graduate School of Medicine, Sakyo-ku, Kyoto 606-8501, Japan.
K Christopher GarciaDepartment of Molecular and Cellular Physiology, Department of Structural Biology, and Howard Hughes Medical Institute, Stanford University School of Medicine, Stanford, CA 94305, USA.
Calvin J KuoDepartment of Medicine, Division of Hematology, Stanford University School of Medicine, Stanford, CA 94305, USA. Electronic address: cjkuo@stanford.edu.
Stanford University · USKyoto University · JPUniversity Hospital Bonn · DE

Funding

Regulation of actively proliferating and quiescent intestinal stem cellsU01DK085527 · NIDDK · STANFORD UNIVERSITY · PI KUO, CALVIN J · 2009 to 2023
$6.9M
Intestinal Stem Cell Consortium Coordinating CenterU01DK085532 · NIDDK · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI NILAND, JOYCE CAROL · 2009 to 2018
$6.5M
Structure-based Bioengineering of Wnt Surrogates for Intestinal Stem Cell Biology and TherapyR01DK115728 · NIDDK · STANFORD UNIVERSITY · PI GARCIA, KENAN CHRISTOPHER, KUO, CALVIN J · 2018 to 2022
$3.9M
Regulation of Blood-Brain Barrier Function by the RECK/GPR124/Wnt7 PathwayR01NS100904 · NINDS · STANFORD UNIVERSITY · PI CALVIN J KUO · 2017 to 2026
$3.6M
Limited Competition for the Continuation of the Intestinal Stem Cell Consortium Coordinating CenterU24DK085532 · NIDDK · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI NILAND, JOYCE CAROL · 2019 to 2023
$2.3M
Regulation of Adult CNS Angiogenesis by GPR124R01NS064517 · NINDS · STANFORD UNIVERSITY · PI KUO, CALVIN J · 2010 to 2014
$1.8M
NIDDK NIH HHS R01 DK115728NIDDK NIH HHS U01 DK085527NIDDK NIH HHS U01 DK085532NIDDK NIH HHS U24 DK085532NINDS NIH HHS R01 NS064517NINDS NIH HHS R01 NS100904
6 · The paper itself

Abstract

WNT7A and WNT7B control CNS angiogenesis and blood-brain barrier formation by activating endothelial Wnt/β-catenin signaling. The GPI-anchored protein RECK and adhesion G protein-coupled receptor GPR124 critically regulate WNT7-specific signaling in concert with FZD and LRP co-receptors. Here, we demonstrate that primarily the GPR124 ectodomain, but not its transmembrane and intracellular domains, mediates RECK/WNT7-induced canonical Wnt signaling. Moreover, RECK is the predominant binding partner of GPR124 in rat brain blood vessels in situ. WNT7A and WNT7B, but not WNT3A, directly bind to purified recombinant soluble RECK, full-length cell surface RECK, and the GPR124:RECK complex. Chemical cross-linking indicates that RECK and WNT7A associate with 1:1 stoichiometry, which stabilizes short-lived, active, monomeric, hydrophobic WNT7A. In contrast, free WNT7A rapidly converts into inactive, hydrophilic aggregates. Overall, RECK is a selective WNT7 receptor that mediates GPR124/FZD/LRP-dependent canonical Wnt/β-catenin signaling by stabilizing active cell surface WNT7, suggesting isoform-specific regulation of Wnt bioavailability.

Indexed as

Animalsbeta CateninBiological AvailabilityBlood-Brain BarrierFemaleFrizzled ReceptorsGPI-Linked ProteinsHEK293 CellsHumansMaleProtein BindingProtein Interaction Domains and MotifsRatsRats, Sprague-DawleyReceptors, G-Protein-CoupledWnt3A ProteinADGRA2 protein, humanbeta CateninCTNNB1 protein, humanFrizzled ReceptorsGPI-Linked ProteinsReceptors, G-Protein-CoupledRECK protein, humanWnt3A ProteinWNT3A protein, humanWNT7A protein, humanWnt Proteinsblood-brain barriercentral nervous systemendothelial cellsGPR124RECKWNT7Wnt signaling

Identifiers

PMID30304675
PMCPMC6338448
OpenAlexW2896541674

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.