Evidence map›Paper›PMID 30016639›Full record

ArticleDevelopmental biology2018

The phenotypic and functional properties of mouse yolk-sac-derived embryonic macrophages.

Nejla Yosef, Tegy J Vadakkan, June-Hee Park, Ross A Poché, Jean-Leon Thomas, Mary E Dickinson

Abstract read
In one paragraph

Article in Developmental biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Origin of Osteoclasts: Osteoclast Precursor Cells.Journal of bone metabolism · 2023
    Article
  6. Article
  7. Microglia and Microglia-Like Cells: Similar but Different.Frontiers in cellular neuroscience · 2022
    Review
  8. Review
  9. Article
  10. Macrophages and the maintenance of homeostasis.Cellular & molecular immunology · 2021
    Review
  11. Article
  12. Article
  13. Article
  14. 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

6 authors.

Nejla YosefDepartment of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, TX, USA.
Tegy J VadakkanDepartment of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, TX, USA.
June-Hee ParkDepartment of Neurology, Yale University, New Haven, CT, USA.
Ross A PochéDepartment of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, TX, USA.
Jean-Leon ThomasDepartment of Neurology, Yale University, New Haven, CT, USA; Sorbonne Universités UPMC Univ Paris 06, Inserm, CNRS, APHP, Institut du Cerveau et de la Moelle épinière (ICM), GH Pitié-Salpêtrière, Paris, France.
Mary E DickinsonDepartment of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, TX, USA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA; Cardiovascular Research Institute, Baylor College of Medicine, Houston, TX, USA; Department of Bioengineering, Rice University, Houston, TX, USA. Electronic address: mdickins@bcm.edu.

Funding

Tumor BiologyP30CA125123 · NCI · BAYLOR COLLEGE OF MEDICINE · PI Michael M Ittmann · 2007 to 2026
$73.9M
Virology CoreP30AI036211 · NIAID · BAYLOR COLLEGE OF MEDICINE · PI BUTEL, JANET S · 1994 to 2015
$21.7M
Neurovascular RegenerationR01EB016629 · NIBIB · YALE UNIVERSITY · PI HIRSCHI, KAREN KEMPER · 2014 to 2018
$4.8M
Specification of Hemogenic Endothelial CellsR01HL128064 · NHLBI · YALE UNIVERSITY · PI DICKINSON, MARY E, HIRSCHI, KAREN KEMPER · 2015 to 2018
$2.6M
BD Biosciences Special Order LSRIIS10RR024574 · NCRR · BAYLOR COLLEGE OF MEDICINE · PI LUMPKIN, ELLEN A · 2009 to 2009
$430k
NCI NIH HHS P30 CA125123NCRR NIH HHS S10 RR024574NHLBI NIH HHS R01 HL128064NIAID NIH HHS P30 AI036211NIBIB NIH HHS R01 EB016629
6 · The paper itself

Abstract

Macrophages are well characterized as immune cells. However, in recent years, a multitude of non-immune functions have emerged many of which play essential roles in a variety of developmental processes (Wynn et al., 2013; DeFalco et al., 2014). In adult animals, macrophages are derived from circulating monocytes originating in the bone marrow, but much of the tissue-resident population arise from erythro-myeloid progenitors (EMPs) in the extra-embryonic yolk sac, appearing around the same time as primitive erythroblasts (Schulz et al., 2012; Kierdorf et al., 2013; McGrath et al., 2015; Gomez Perdiguero et al., 2015; Mass et al., 2016). Of particular interest to our group, macrophages have been shown to act as pro-angiogenic regulators during development (Wynn et al., 2013; DeFalco et al., 2014; Hsu et al., 2015), but there is still much to learn about these early cells. The goal of the present study was to isolate and expand progenitors of yolk-sac-derived Embryonic Macrophages (EMs) in vitro to generate a new platform for mechanistic studies of EM differentiation. To accomplish this goal, we isolated pure (>98%) EGFP

Indexed as

AnimalsCell Culture TechniquesCell DifferentiationCoculture TechniquesErythroid Precursor CellsFlow CytometryHematopoietic Stem CellsMacrophagesMiceMyeloid Progenitor CellsPhenotypeYolk SacAngiogenesisEndothelial CellsMacrophagesMicrogliaNeural Stem/Progenitor CellsYolk sac

Identifiers

PMID30016639
PMCPMC6190604

What OpenQuestion holds

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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.