Evidence map›Paper›PMID 27475716›Full record

ArticleBiochemical pharmacology2016

A novel real time imaging platform to quantify macrophage phagocytosis.

Theodore S Kapellos, Lewis Taylor, Heyne Lee, Sally A Cowley, William S James, Asif J Iqbal, David R Greaves

Open access · hybridAbstract readComparative StudyValidation Study
In one paragraph

Article in Biochemical pharmacology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 85 papers.

0numbers the graph read from it
0cells of the map it votes in
85citing papers in PubMed
5.8field-weighted citation impact, top 3% 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

85 citing papers in PubMed, 142 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Phagocytosis ofInternational journal of molecular sciences · 2026
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  12. InactivatedFrontiers in immunology · 2025
    Article
  13. Heterogeneity ofInfection and immunity · 2024
    Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. The ketone body β-hydroxybutyrate shifts microglial metabolism and suppresses amyloid-β oligomer-induced inflammation in human microglia.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2023
    Article
  19. Article
  20. Article

25 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

7 authors at 1 institution in 1 country.

Theodore S KapellosSir William Dunn School of Pathology, South Parks Road, OX1 3RE Oxford, UK.
Lewis TaylorSir William Dunn School of Pathology, South Parks Road, OX1 3RE Oxford, UK.
Heyne LeeSir William Dunn School of Pathology, South Parks Road, OX1 3RE Oxford, UK.
Sally A CowleySir William Dunn School of Pathology, South Parks Road, OX1 3RE Oxford, UK.
William S JamesSir William Dunn School of Pathology, South Parks Road, OX1 3RE Oxford, UK.
Asif J IqbalSir William Dunn School of Pathology, South Parks Road, OX1 3RE Oxford, UK.
David R GreavesSir William Dunn School of Pathology, South Parks Road, OX1 3RE Oxford, UK. Electronic address: david.greaves@hertford.ox.ac.uk.
Science Oxford · GB

Funding

British Heart Foundation RG/15/10/31485Medical Research Council MR/M024962/1Parkinson's UK J-0901
6 · The paper itself

Abstract

Phagocytosis of pathogens, apoptotic cells and debris is a key feature of macrophage function in host defense and tissue homeostasis. Quantification of macrophage phagocytosis in vitro has traditionally been technically challenging. Here we report the optimization and validation of the IncuCyte ZOOM® real time imaging platform for macrophage phagocytosis based on pHrodo® pathogen bioparticles, which only fluoresce when localized in the acidic environment of the phagolysosome. Image analysis and fluorescence quantification were performed with the automated IncuCyte™ Basic Software. Titration of the bioparticle number showed that the system is more sensitive than a spectrofluorometer, as it can detect phagocytosis when using 20× less E. coli bioparticles. We exemplified the power of this real time imaging platform by studying phagocytosis of murine alveolar, bone marrow and peritoneal macrophages. We further demonstrate the ability of this platform to study modulation of the phagocytic process, as pharmacological inhibitors of phagocytosis suppressed bioparticle uptake in a concentration-dependent manner, whereas opsonins augmented phagocytosis. We also investigated the effects of macrophage polarization on E. coli phagocytosis. Bone marrow-derived macrophage (BMDM) priming with M2 stimuli, such as IL-4 and IL-10 resulted in higher engulfment of bioparticles in comparison with M1 polarization. Moreover, we demonstrated that tolerization of BMDMs with lipopolysaccharide (LPS) results in impaired E. coli bioparticle phagocytosis. This novel real time assay will enable researchers to quantify macrophage phagocytosis with a higher degree of accuracy and sensitivity and will allow investigation of limited populations of primary phagocytes in vitro.

Indexed as

PhagocytosisAnimalsBone Marrow CellsCell-Derived MicroparticlesCell LineCells, CulturedEndotoxinsEscherichia coliHumansImage Processing, Computer-AssistedInduced Pluripotent Stem CellsInterleukinsMacrophage ActivationMacrophagesMacrophages, AlveolarMacrophages, Peritonealendotoxin, Escherichia coliEndotoxinsInterleukinsOpsonin ProteinsBafilomycin A1 (PubChem CID: 6375210)Cytochalasin D (PubChem CID: 5458428)InflammationLPSMacrophageNocodazole (PubChem CID: 4122)Phagocytosis

Identifiers

PMID27475716
PMCPMC5012892
OpenAlexW2500542777

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.