Evidence map›Paper›PMID 25119047›Full record

ArticleNature2014

Jam1a-Jam2a interactions regulate haematopoietic stem cell fate through Notch signalling.

Isao Kobayashi, Jingjing Kobayashi-Sun, Albert D Kim, Claire Pouget, Naonobu Fujita, Toshio Suda, David Traver

Abstract read
In one paragraph

Article in Nature, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 102 papers.

0numbers the graph read from it
0cells of the map it votes in
102citing papers in PubMed
6.4field-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

102 citing papers in PubMed, 173 citations in OpenAlex.

  1. Article
  2. Gpr171 regulates embryonic hematopoietic stem cell emergence via ERK1/2 and Notch signaling.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Article
  4. Review
  5. Article
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  8. Article
  9. Article
  10. Characterizing the Ovarian Cytogenetic Dynamics of Sichuan Bream (International journal of molecular sciences · 2025
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Science advances · 2024
    Article
  19. Article
  20. Inflammation in Development and Aging: Insights from the Zebrafish Model.International journal of molecular sciences · 2024
    Review

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 2 countries.

Isao KobayashiDepartment of Cellular and Molecular Medicine, University of California, San Diego, La Jolla, California 92093-0380, USA.
Jingjing Kobayashi-SunDepartment of Cellular and Molecular Medicine, University of California, San Diego, La Jolla, California 92093-0380, USA.
Albert D KimDepartment of Cellular and Molecular Medicine, University of California, San Diego, La Jolla, California 92093-0380, USA.
Claire PougetDepartment of Cellular and Molecular Medicine, University of California, San Diego, La Jolla, California 92093-0380, USA.
Naonobu FujitaSection of Cell and Developmental Biology, University of California, San Diego, La Jolla, California 92093-0380, USA.
Toshio SudaDepartment of Cell Differentiation, The Sakaguchi Laboratory, School of Medicine, Keio University, Shinjukuku, Tokyo 160-8582, Japan.
David Traver1] Department of Cellular and Molecular Medicine, University of California, San Diego, La Jolla, California 92093-0380, USA [2] Section of Cell and Developmental Biology, University of California, San Diego, La Jolla, California 92093-0380, USA.
University of California, San Diego · USKeio University · JP

Funding

Molecular and functional dissection of zebrafish hematopoietic stem cell nicheR01DK074482 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI TRAVER, DAVID · 2006 to 2024
$6.5M
NIDDK NIH HHS R01 DK074482NIDDK NIH HHS R01-DK074482
6 · The paper itself

Abstract

Notch signalling plays a key role in the generation of haematopoietic stem cells (HSCs) during vertebrate development and requires intimate contact between signal-emitting and signal-receiving cells, although little is known regarding when, where and how these intercellular events occur. We previously reported that the somitic Notch ligands, Dlc and Dld, are essential for HSC specification. It has remained unclear, however, how these somitic requirements are connected to the later emergence of HSCs from the dorsal aorta. Here we show in zebrafish that Notch signalling establishes HSC fate as their shared vascular precursors migrate across the ventral face of the somite and that junctional adhesion molecules (JAMs) mediate this required Notch signal transduction. HSC precursors express jam1a (also known as f11r) and migrate axially across the ventral somite, where Jam2a and the Notch ligands Dlc and Dld are expressed. Despite no alteration in the expression of Notch ligand or receptor genes, loss of function of jam1a led to loss of Notch signalling and loss of HSCs. Enforced activation of Notch in shared vascular precursors rescued HSCs in jam1a or jam2a deficient embryos. Together, these results indicate that Jam1a-Jam2a interactions facilitate the transduction of requisite Notch signals from the somite to the precursors of HSCs, and that these events occur well before formation of the dorsal aorta.

Indexed as

Signal TransductionAnimalsAortaCell DifferentiationCell MovementHematopoietic Stem CellsJunctional Adhesion Molecule AJunctional Adhesion Molecule BPhenotypeReceptors, Cell SurfaceReceptors, NotchSomitesZebrafishZebrafish Proteinsf11r.1 protein, zebrafishJam2a protein, zebrafishJunctional Adhesion Molecule AJunctional Adhesion Molecule BReceptors, Cell SurfaceReceptors, NotchZebrafish Proteins

Identifiers

PMID25119047
PMCPMC4237229
OpenAlexW2045791261

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.