Evidence map›Paper›PMID 30758286›Full record

ArticleeLife2019

Macrophages restrict the nephrogenic field and promote endothelial connections during kidney development.

David AD Munro, Yishay Wineberg, Julia Tarnick, Chris S Vink, Zhuan Li, Clare Pridans, Elaine Dzierzak, Tomer Kalisky, Peter Hohenstein, Jamie A Davies

Open access · goldAbstract read
In one paragraph

Article in eLife, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

47 citing papers in PubMed, 80 citations in OpenAlex.

  1. Review
  2. Review
  3. Macrophages in embryonic development.Nature reviews. Immunology · 2026
    Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Review
  14. Leukocyte-lymphatic intersections during cardiac inflammation.Journal of molecular and cellular cardiology · 2025
    Review
  15. Review
  16. Review
  17. Article
  18. Organoids and tissue/organ chips.Stem cell research & therapy · 2024
    Article
  19. Article
  20. Kidney resident macrophages have distinct subsets and multifunctional roles.Matrix biology : journal of the International Society for Matrix Biology · 2024
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 3 countries.

David AD MunroCentre for Discovery Brain Sciences, The University of Edinburgh, Edinburgh, United Kingdom.ORCID 0000-0002-3521-2121
Yishay WinebergDepartment of Bioengineering, Bar-Ilan University, Ramat Gan, Israel.
Julia TarnickCentre for Discovery Brain Sciences, The University of Edinburgh, Edinburgh, United Kingdom.
Chris S VinkCentre for Inflammation Research, Queen's Medical Research Institute, The University of Edinburgh, Edinburgh, United Kingdom.
Zhuan LiCentre for Inflammation Research, Queen's Medical Research Institute, The University of Edinburgh, Edinburgh, United Kingdom.
Clare PridansCentre for Inflammation Research, Queen's Medical Research Institute, The University of Edinburgh, Edinburgh, United Kingdom.ORCID 0000-0001-9423-557X
Elaine DzierzakCentre for Inflammation Research, Queen's Medical Research Institute, The University of Edinburgh, Edinburgh, United Kingdom.
Tomer KaliskyDepartment of Bioengineering, Bar-Ilan University, Ramat Gan, Israel.ORCID 0000-0003-4733-262X
Peter HohensteinLeiden University Medical Center, Leiden University, Leiden, The Netherlands.
Jamie A DaviesCentre for Discovery Brain Sciences, The University of Edinburgh, Edinburgh, United Kingdom.ORCID 0000-0001-6660-4032
Queen's Medical Centre · GBUniversity of Edinburgh · GBBar-Ilan University · ILRoslin Institute · GB

Funding

Biotechnology and Biological Sciences Research Council BB/P013732/1Medical Research Council MR/K501293/1
6 · The paper itself

Abstract

The origins and functions of kidney macrophages in the adult have been explored, but their roles during development remain largely unknown. Here we characterise macrophage arrival, localisation, heterogeneity, and functions during kidney organogenesis. Using genetic approaches to ablate macrophages, we identify a role for macrophages in nephron progenitor cell clearance as mouse kidney development begins. Throughout renal organogenesis, most kidney macrophages are perivascular and express F4/80 and CD206. These macrophages are enriched for mRNAs linked to developmental processes, such as blood vessel morphogenesis. Using antibody-mediated macrophage-depletion, we show macrophages support vascular anastomoses in cultured kidney explants. We also characterise a subpopulation of galectin-3

Indexed as

AnimalsCalcium-Binding ProteinsCell LineageGalectin 3Gene Expression Regulation, DevelopmentalKidneyLectins, C-TypeMacrophagesMannose-Binding LectinsMannose ReceptorMiceNephronsOrganogenesisReceptors, Cell SurfaceReceptors, G-Protein-CoupledStem CellsAdgre1 protein, mouseCalcium-Binding ProteinsGalectin 3Lectins, C-TypeLgals3 protein, mouseMannose-Binding LectinsMannose ReceptorReceptors, Cell SurfaceReceptors, G-Protein-Coupledblood vesselcell migrationdevelopmental biologyhumanmorphogenesismousenephronphagocytosis

Identifiers

PMID30758286
PMCPMC6374076
OpenAlexW2913851546

What OpenQuestion holds

Textmetadata
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.