Evidence map›Paper›PMID 27262757›Full record

ArticleJournal of hepatology2016

Bone marrow-derived and resident liver macrophages display unique transcriptomic signatures but similar biological functions.

Lynette Beattie, Amy Sawtell, Jason Mann, Teija C M Frame, Bianca Teal, Fabian de Labastida Rivera, Najmeeyah Brown, Katherine Walwyn-Brown, John W J Moore, Sandy MacDonald and 5 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of hepatology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 148 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
148citing papers in PubMed, 1 pooled it
9.6field-weighted citation impact, top 1% 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

148 citing papers in PubMed, 1 synthesis or guideline pooled it, 250 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Liver Macrophages in the Pathogenesis of Viral Hepatitis.Current issues in molecular biology · 2026
    Review
  5. Review
  6. Kupffer cells: Orchestrators of liver physiology.Liver research (Beijing, China) · 2026
    Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Myeloid cells in chronic liver inflammation.Cellular & molecular immunology · 2025
    Review
  15. Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article

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

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 at 3 institutions in 2 countries.

Lynette BeattieCentre for Immunology and Infection, Hull York Medical School and Dept. of Biology, University of York, York YO10 5DD, UK; QIMR Berghofer Medical Research Institute, 300 Herston Rd, Herston, Queensland 4006, Australia.
Amy SawtellCentre for Immunology and Infection, Hull York Medical School and Dept. of Biology, University of York, York YO10 5DD, UK.
Jason MannCentre for Immunology and Infection, Hull York Medical School and Dept. of Biology, University of York, York YO10 5DD, UK.
Teija C M FrameQIMR Berghofer Medical Research Institute, 300 Herston Rd, Herston, Queensland 4006, Australia.
Bianca TealQIMR Berghofer Medical Research Institute, 300 Herston Rd, Herston, Queensland 4006, Australia.
Fabian de Labastida RiveraQIMR Berghofer Medical Research Institute, 300 Herston Rd, Herston, Queensland 4006, Australia.
Najmeeyah BrownCentre for Immunology and Infection, Hull York Medical School and Dept. of Biology, University of York, York YO10 5DD, UK.
Katherine Walwyn-BrownCentre for Immunology and Infection, Hull York Medical School and Dept. of Biology, University of York, York YO10 5DD, UK.
John W J MooreCentre for Immunology and Infection, Hull York Medical School and Dept. of Biology, University of York, York YO10 5DD, UK.
Sandy MacDonaldBiosciences Technology Facility, Dept. of Biology, University of York, York YO10 5DD, UK.
Eng-Kiat LimCentre for Immunology and Infection, Hull York Medical School and Dept. of Biology, University of York, York YO10 5DD, UK.
Jane E DaltonCentre for Immunology and Infection, Hull York Medical School and Dept. of Biology, University of York, York YO10 5DD, UK.
Christian R EngwerdaQIMR Berghofer Medical Research Institute, 300 Herston Rd, Herston, Queensland 4006, Australia.
Kelli P MacDonaldQIMR Berghofer Medical Research Institute, 300 Herston Rd, Herston, Queensland 4006, Australia.
Paul M KayeCentre for Immunology and Infection, Hull York Medical School and Dept. of Biology, University of York, York YO10 5DD, UK. Electronic address: paul.kaye@york.ac.uk.
Hull York Medical School · GBQIMR Berghofer Medical Research Institute · AUUniversity of York · GB

Funding

Medical Research Council G0400786Medical Research Council G0802620Medical Research Council G1000230
6 · The paper itself

Abstract

BACKGROUND &

aimsKupffer cells (KCs), the resident tissue macrophages of the liver, play a crucial role in the clearance of pathogens and other particulate materials that reach the systemic circulation. Recent studies have identified KCs as a yolk sac-derived resident macrophage population that is replenished independently of monocytes in the steady state. Although it is now established that following local tissue injury, bone marrow derived monocytes may infiltrate the tissue and differentiate into macrophages, the extent to which newly differentiated macrophages functionally resemble the KCs they have replaced has not been extensively studied.

methodsWe studied the two populations of KCs using intravital microscopy, morphometric analysis and gene expression profiling. An ion homeostasis gene signature, including genes associated with scavenger receptor function and extracellular matrix deposition, allowed discrimination between these two KC sub-types.

resultsBone marrow derived "KCs" accumulating as a result of genotoxic injury, resemble but are not identical to their yolk sac counterparts. Reflecting the differential expression of scavenger receptors, yolk sac-derived KCs were more effective at accumulating acetylated low density lipoprotein, whereas surprisingly, they were poorer than bone marrow-derived KCs when assessed for uptake of a range of bacterial pathogens. The two KC populations were almost indistinguishable in regard to i) response to lipopolysaccharide challenge, ii) phagocytosis of effete red blood cells and iii) their ability to contain infection and direct granuloma formation against Leishmania donovani, a KC-tropic intracellular parasite.

conclusionsBone marrow-derived KCs differentiate locally to resemble yolk sac-derived KC in most but not all respects, with implications for models of infectious diseases, liver injury and bone marrow transplantation. In addition, the gene signature we describe adds to the tools available for distinguishing KC subpopulations based on their ontology. LAY SUMMARY: Liver macrophages play a major role in the control of infections in the liver and in the pathology associated with chronic liver diseases. It was recently shown that liver macrophages can have two different origins, however, the extent to which these populations are functionally distinct remains to be fully addressed. Our study demonstrates that whilst liver macrophages share many features in common, regardless of their origin, some subtle differences in function exist. DATA REPOSITORY: Gene expression data are available from the European Bioinformatics Institute ArrayExpress data repository (accession number E-MTAB-4954).

Indexed as

Bone MarrowHumansKupffer CellsLiverMacrophagesMonocytesKupffer cellsLeishmaniaListeriaLiver macrophagesNeisseriaSalmonellaScavenger receptors

Identifiers

PMID27262757
PMCPMC5028381
OpenAlexW2418111900

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.