Evidence map›Paper›PMID 39217144›Full record

ArticleNature communications2024

The heart is a resident tissue for hematopoietic stem and progenitor cells in zebrafish.

Dorothee Bornhorst, Amulya V Hejjaji, Lena Steuter, Nicole M Woodhead, Paul Maier, Alessandra Gentile, Alice Alhajkadour, Octavia Santis Larrain, Michael Weber, Khrievono Kikhi and 5 more

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
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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.

Dorothee BornhorstInstitute of Cell Biology, Faculty of Medicine, University of Münster, Münster, 48149, Germany.ORCID 0000-0003-4084-0250
Amulya V Hejjaji *Institute of Cell Biology, Faculty of Medicine, University of Münster, Münster, 48149, Germany.ORCID 0009-0001-2510-5242
Lena Steuter *Institute of Cell Biology, Faculty of Medicine, University of Münster, Münster, 48149, Germany.
Nicole M WoodheadDepartment of Cell and Regenerative Biology, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI, 53705, USA.
Paul MaierMultiscale Biology, Faculty of Biology and Psychology, Georg-August-University Göttingen, Göttingen, 37077, Germany.
Alessandra GentileDepartment of Developmental Genetics, Max Planck Institute for Heart and Lung Research (MPI-HLR), Bad Nauheim, 61231, Germany.ORCID 0000-0002-5423-7295
Alice AlhajkadourDepartment of Cell and Regenerative Biology, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI, 53705, USA.ORCID 0009-0001-8006-2732
Octavia Santis LarrainDepartment of Cell and Regenerative Biology, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI, 53705, USA.ORCID 0000-0002-6907-4564
Michael WeberMultiscale Biology, Faculty of Biology and Psychology, Georg-August-University Göttingen, Göttingen, 37077, Germany.ORCID 0000-0001-8007-9975
Khrievono KikhiFlow Cytometry and Cell Sorting Core Facility, MPI-HLR, Bad Nauheim, 61231, Germany.ORCID 0000-0001-5672-3791
Stefan GuentherDeep Sequencing Platform, MPI-HLR, Bad Nauheim, 61231, Germany.ORCID 0000-0002-5594-4549
Jan HuiskenMultiscale Biology, Faculty of Biology and Psychology, Georg-August-University Göttingen, Göttingen, 37077, Germany.
Owen J TamplinDepartment of Cell and Regenerative Biology, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI, 53705, USA.ORCID 0000-0001-9146-4860
Didier Y R StainierDepartment of Developmental Genetics, Max Planck Institute for Heart and Lung Research (MPI-HLR), Bad Nauheim, 61231, Germany.ORCID 0000-0002-0382-0026
Felix GunawanInstitute of Cell Biology, Faculty of Medicine, University of Münster, Münster, 48149, Germany. felix.gunawan@ukmuenster.de.ORCID 0000-0002-5592-9680

Funding

Improving the interaction of hematopoietic stem cells with the perivascular niche to promote engraftmentR01HL142998 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI TAMPLIN, OWEN JAMES · 2018 to 2022
$2.3M
Reprogramming of hematopoietic stem cells during contact with the perivascular nicheR01HL174965 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI Owen James Tamplin · 2024 to 2026
$1.5M
Improving the interaction of hematopoietic stem cells with the perivascular niche to promote engraftmentR56HL142998 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI TAMPLIN, OWEN JAMES · 2023 to 2023
$538k
American Society of Hematology BridgeNHLBI NIH HHS R01 HL142998NHLBI NIH HHS R01 HL174965NHLBI NIH HHS R56 HL142998University of Münster | Medizinische Fakultät, Westfälische Wilhelms-Universität Münster (Medical Faculty, WWU Münster) I-GU122208University of Münster; the Innovative Medical Research
6 · The paper itself

Abstract

The contribution of endocardial cells (EdCs) to the hematopoietic lineages has been strongly debated. Here, we provide evidence that in zebrafish, the endocardium gives rise to and maintains a stable population of hematopoietic cells. Using single-cell sequencing, we identify an endocardial subpopulation expressing enriched levels of hematopoietic-promoting genes. High-resolution microscopy and photoconversion tracing experiments uncover hematopoietic cells, mainly hematopoietic stem and progenitor cells (HSPCs)/megakaryocyte-erythroid precursors (MEPs), derived from EdCs as well as the dorsal aorta stably attached to the endocardium. Emergence of HSPCs/MEPs in hearts cultured ex vivo without external hematopoietic sources, as well as longitudinal imaging of the beating heart using light sheet microscopy, support endocardial contribution to hematopoiesis. Maintenance of these hematopoietic cells depends on the adhesion factors Integrin α4 and Vcam1 but is at least partly independent of cardiac trabeculation or shear stress. Finally, blocking primitive erythropoiesis increases cardiac-residing hematopoietic cells, suggesting that the endocardium is a hematopoietic reservoir. Altogether, these studies uncover the endocardium as a resident tissue for HSPCs/MEPs and a de novo source of hematopoietic cells.

Indexed as

EndocardiumHematopoietic Stem CellsZebrafishAnimalsAnimals, Genetically ModifiedCell LineageErythropoiesisHeartHematopoiesisSingle-Cell AnalysisVascular Cell Adhesion Molecule-1Zebrafish ProteinsVascular Cell Adhesion Molecule-1Zebrafish Proteins

Identifiers

PMID39217144
PMCPMC11366026

What OpenQuestion holds

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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.