Evidence map›Paper›PMID 31110287›Full record

ArticleNature cell biology2019

EGFR is required for Wnt9a-Fzd9b signalling specificity in haematopoietic stem cells.

Stephanie Grainger, Nicole Nguyen, Jenna Richter, Jordan Setayesh, Brianna Lonquich, Chet Huan Oon, Jacob M Wozniak, Rocio Barahona, Caramai N Kamei, Jack Houston and 5 more

Abstract read
In one paragraph

Article in Nature cell biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

44 citing papers in PubMed, 63 citations in OpenAlex.

  1. Article
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  8. Review
  9. Article
  10. Unleashing Wnts: Wnt Ligands Fuel Cancer Spread.Journal of cancer biology · 2025
    Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Learning from Zebrafish Hematopoiesis.Advances in experimental medicine and biology · 2023
    Review
  19. Wnt regulation of hematopoietic stem cell development and disease.Current topics in developmental biology · 2023
    Review
  20. Article
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

15 authors at 3 institutions in 1 country.

Stephanie GraingerDepartment of Cellular and Molecular Medicine, University of California, San Diego, La Jolla, CA, USA.
Nicole NguyenDepartment of Cellular and Molecular Medicine, University of California, San Diego, La Jolla, CA, USA.
Jenna RichterDepartment of Cellular and Molecular Medicine, University of California, San Diego, La Jolla, CA, USA.
Jordan SetayeshDepartment of Cellular and Molecular Medicine, University of California, San Diego, La Jolla, CA, USA.
Brianna LonquichDepartment of Cellular and Molecular Medicine, University of California, San Diego, La Jolla, CA, USA.
Chet Huan OonDepartment of Cellular and Molecular Medicine, University of California, San Diego, La Jolla, CA, USA.
Jacob M WozniakBiomedical Sciences Graduate Program, University of California, San Diego, La Jolla, CA, USA.
Rocio BarahonaDepartment of Cellular and Molecular Medicine, University of California, San Diego, La Jolla, CA, USA.
Caramai N KameiMassachusetts General Hospital Nephrology Division, Charlestown, MA, USA.
Jack HoustonDepartment of Cellular and Molecular Medicine, University of California, San Diego, La Jolla, CA, USA.
Marvic Carrillo-TerrazasSkaggs School of Pharmacy and Pharmaceutical Science, University of California, San Diego, La Jolla, CA, USA.
Iain A DrummondMassachusetts General Hospital Nephrology Division, Charlestown, MA, USA.
David GonzalezSkaggs School of Pharmacy and Pharmaceutical Science, University of California, San Diego, La Jolla, CA, USA.
Karl WillertDepartment of Cellular and Molecular Medicine, University of California, San Diego, La Jolla, CA, USA. kwillert@ucsd.edu.ORCID http://orcid.org/0000-0002-8020-6804
David TraverDepartment of Cellular and Molecular Medicine, University of California, San Diego, La Jolla, CA, USA. dtraver@ucsd.edu.ORCID http://orcid.org/0000-0002-9652-7653
University of California San Diego · USHarvard University · USMassachusetts General Hospital · US

Funding

GRADUATE TRAINING IN CELLULAR &MOLECULAR PHARMACOLOGYT32GM007752 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI BROWN, JOAN HELLER, HANDEL, TRACY M · 1985 to 2023
$13.5M
Wnt signaling in hematopoietic developmentR01HL135205 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI TRAVER, DAVID, WILLERT, KARL H · 2017 to 2024
$4.9M
Rheumatic Diseases Research Training GrantT32AR064194 · NIAMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GARY S FIRESTEIN, Monica Guma · 2013 to 2026
$3.8M
Exploring Wnt-Fzd signaling specificitiesR35GM134961 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI WILLERT, KARL H · 2020 to 2024
$2.3M
Analyzing the role of Wnt signaling in pluripotencyR01GM110304 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI WILLERT, KARL H · 2014 to 2019
$1.8M
Mechanisms of tubule interconnectionUH3DK107372 · NIDDK · MOUNT DESERT ISLAND BIOLOGICAL LAB · PI DRUMMOND, IAIN A. · 2017 to 2019
$1.3M
The Role of Wnt Signaling in Normal and Abnormal HematopoiesisR00HL133458 · NHLBI · VAN ANDEL RESEARCH INSTITUTE · PI GRAINGER, STEPHANIE LAURA · 2019 to 2021
$990k
Mechanisms of tubule interconnectionUH2DK107372 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI DRUMMOND, IAIN A. · 2015 to 2016
$725k
The Role of Wnt Signaling in Normal and Abnormal HematopoiesisK99HL133458 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GRAINGER, STEPHANIE LAURA · 2017 to 2018
$292k
NHLBI NIH HHS K99 HL133458NHLBI NIH HHS R00 HL133458NHLBI NIH HHS R01 HL135205NIAMS NIH HHS T32 AR064194NIDDK NIH HHS UH2 DK107372NIDDK NIH HHS UH3 DK107372NIGMS NIH HHS R01 GM110304NIGMS NIH HHS R35 GM134961NIGMS NIH HHS T32 GM007752
6 · The paper itself

Abstract

Wnt signalling drives many processes in development, homeostasis and disease; however, the role and mechanism of individual ligand-receptor (Wnt-Frizzled (Fzd)) interactions in specific biological processes remain poorly understood. Wnt9a is specifically required for the amplification of blood progenitor cells during development. Using genetic studies in zebrafish and human embryonic stem cells, paired with in vitro cell biology and biochemistry, we determined that Wnt9a signals specifically through Fzd9b to elicit β-catenin-dependent Wnt signalling that regulates haematopoietic stem and progenitor cell emergence. We demonstrate that the epidermal growth factor receptor (EGFR) is required as a cofactor for Wnt9a-Fzd9b signalling. EGFR-mediated phosphorylation of one tyrosine residue on the Fzd9b intracellular tail in response to Wnt9a promotes internalization of the Wnt9a-Fzd9b-LRP signalosome and subsequent signal transduction. These findings provide mechanistic insights for specific Wnt-Fzd signals, which will be crucial for specific therapeutic targeting and regenerative medicine.

Indexed as

Animalsbeta CateninErbB ReceptorsHematopoietic Stem CellsHumansPhosphorylationReceptors, NeurotransmitterWnt ProteinsWnt Signaling PathwayZebrafishZebrafish Proteinsbeta CateninCTNNB1 protein, humanEGFR protein, humanErbB ReceptorsFzd3a protein, zebrafishReceptors, NeurotransmitterWnt9a protein, zebrafishWnt ProteinsZebrafish Proteins

Identifiers

PMID31110287
PMCPMC6559346
OpenAlexW2946028463

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.