Evidence map›Paper›PMID 35288551›Full record

ArticleNature communications2022

A specialized bone marrow microenvironment for fetal haematopoiesis.

Yang Liu, Qi Chen, Hyun-Woo Jeong, Bong Ihn Koh, Emma C Watson, Cong Xu, Martin Stehling, Bin Zhou, Ralf H Adams

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
7.5field-weighted citation impact, top 2% 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

28 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
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  10. Review
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  13. HES1 is required for mouse fetal hematopoiesis.Stem cell research & therapy · 2024
    Article
  14. Article
  15. Article
  16. Complementary and Inducible creERStem cell reviews and reports · 2024
    Article
  17. Article
  18. The evolving hematopoietic niche during development.Frontiers in molecular biosciences · 2024
    Review
  19. Article
  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

9 authors at 3 institutions in 3 countries.

Yang Liu *Max Planck Institute for Molecular Biomedicine, Department of Tissue Morphogenesis, University of Münster, Faculty of Medicine, Münster, D-48149, Germany. yangl005@scut.edu.cn.ORCID http://orcid.org/0000-0002-4989-2404
Qi Chen *Max Planck Institute for Molecular Biomedicine, Department of Tissue Morphogenesis, University of Münster, Faculty of Medicine, Münster, D-48149, Germany.ORCID http://orcid.org/0000-0001-8485-6540
Hyun-Woo Jeong *Max Planck Institute for Molecular Biomedicine, Department of Tissue Morphogenesis, University of Münster, Faculty of Medicine, Münster, D-48149, Germany.ORCID http://orcid.org/0000-0002-6976-6739
Bong Ihn KohMax Planck Institute for Molecular Biomedicine, Department of Tissue Morphogenesis, University of Münster, Faculty of Medicine, Münster, D-48149, Germany.
Emma C WatsonMax Planck Institute for Molecular Biomedicine, Department of Tissue Morphogenesis, University of Münster, Faculty of Medicine, Münster, D-48149, Germany.ORCID http://orcid.org/0000-0002-0986-5524
Cong XuMax Planck Institute for Molecular Biomedicine, Department of Tissue Morphogenesis, University of Münster, Faculty of Medicine, Münster, D-48149, Germany.
Martin StehlingFlow Cytometry Unit, Max Planck Institute for Molecular Biomedicine, Münster, D-48149, Germany.
Bin ZhouState Key Laboratory of Cell Biology, CAS Center for Excellence in Molecular Cell Science, Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences, 320 Yueyang Road, A-2112, Shanghai, 200031, China.ORCID http://orcid.org/0000-0001-5278-5522
Ralf H AdamsMax Planck Institute for Molecular Biomedicine, Department of Tissue Morphogenesis, University of Münster, Faculty of Medicine, Münster, D-48149, Germany. ralf.adams@mpi-muenster.mpg.de.ORCID http://orcid.org/0000-0003-3031-7677
University of Münster · DEChinese Academy of Sciences · CNMax Planck Institute for Molecular Biomedicine · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In adult mammalian bone marrow (BM), vascular endothelial cells and perivascular reticular cells control the function of haematopoietic stem and progenitor cells (HSPCs). During fetal development, the mechanisms regulating the de novo haematopoietic cell colonization of BM remain largely unknown. Here, we show that fetal and adult BM exhibit fundamental differences in cellular composition and molecular interactions by single cell RNA sequencing. While fetal femur is largely devoid of leptin receptor-expressing cells, arterial endothelial cells (AECs) provide Wnt ligand to control the initial HSPC expansion. Haematopoietic stem cells and c-Kit

Indexed as

Bone MarrowEndothelial CellsAnimalsBone Marrow CellsFetusHematopoiesisHematopoietic Stem CellsMammals

Identifiers

PMID35288551
PMCPMC8921288
OpenAlexW4221119346

What OpenQuestion holds

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LicenceCC BY
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.