Evidence map›Paper›PMID 10722588›Full record

ArticleInfection and immunity2000

Macrophage class A scavenger receptor-mediated phagocytosis of Escherichia coli: role of cell heterogeneity, microbial strain, and culture conditions in vitro.

L Peiser, P J Gough, T Kodama, S Gordon

Abstract readComparative Study
In one paragraph

Article in Infection and immunity, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed
3.4field-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

80 citing papers in PubMed, 234 citations in OpenAlex.

  1. PostbioticFrontiers in immunology · 2026
    Article
  2. Cyclic Strain and Macrophage-Mediated Transport Govern Micron-Sized PMAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  3. Article
  4. Phagocytosis.Methods in molecular biology (Clifton, N.J.) · 2024
    Review
  5. Inhibition of Phagocytosis by Silibinin in Mouse Macrophages.Current issues in molecular biology · 2023
    Article
  6. Article
  7. Emerging Concepts in Defective Macrophage Phagocytosis in Cystic Fibrosis.International journal of molecular sciences · 2022
    Review
  8. Article
  9. Shiga Toxin-ProducingMicroorganisms · 2022
    Review
  10. Review
  11. Review
  12. Scavenger receptor A1 participates in uptake ofEmerging microbes & infections · 2021
    Article
  13. Article
  14. Modulation Effects ofVaccines · 2020
    Article
  15. Article
  16. International journal of molecular sciences · 2020
    Article
  17. Review
  18. Article
  19. Article
  20. Review

20 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

4 authors at 2 institutions in 2 countries.

L PeiserSir William Dunn School of Pathology, University of Oxford, Oxford OX1 3RE, United Kingdom. leanne.peiser@path.ox.ac.uk
P J Gough
T Kodama
S Gordon
University of Oxford · GBThe University of Tokyo · JP

Funding

Wellcome Trust
6 · The paper itself

Abstract

Macrophage class A scavenger receptors (SR-AI and SR-AII) contribute to host defense by binding polyanionic ligands such as lipopolysaccharide and lipoteichoic acid. SR-A knockout (SR-A(-/-)) mice are more susceptible to endotoxic shock and Listeria monocytogenes infection in vivo, possibly due to decreased clearance of lipopolysaccharide and microorganisms, respectively. We have used flow cytometry to analyze the role of SR-A and other scavenger-like receptors in phagocytosis of bacteria in vitro. Chinese hamster ovary cells stably transfected with human SR-A bound Escherichia coli and Staphylococcus aureus but ingested few organisms. Primary human monocyte-derived macrophages (Mphi) bound and ingested E. coli more efficiently, and this was partially but selectively blocked by the general SR inhibitor, poly(I). A specific and selective role for SR-A was shown, since bone marrow culture-derived Mphi from SR-A(-/-) mice ingested fewer E. coli organisms than did wild-type cells, while uptake of antibody-opsonized E. coli was unaffected. SR-A-dependent uptake of E. coli varied with the bacterial strain; ingestion of DH5alpha and K1 by SR-A(-/-) Mphi was reduced by 30 to 60% and 70 to 75%, respectively. Phagocytosis and endocytosis via SR-A were markedly down-modulated when Mphi were plated on serum-coated tissue culture plastic compared to bacteriologic plastic, where cell adhesion is mediated by SR-A and CR3, respectively. This paper demonstrates that SR-A can bind and ingest bacteria directly, consistent with a role in host defense in vivo, and highlights the importance of the source of the Mphi, bacterial strain, and culture conditions on receptor function in vitro.

Indexed as

AnimalsBacterial AdhesionBone Marrow CellsCell LineCells, CulturedCHO CellsCricetinaeEscherichia coliFlow CytometryHumansMacrophagesMiceMice, Inbred ICRMice, KnockoutMicroscopy, FluorescenceMonocytesMSR1 protein, humanMsr1 protein, mouseProtein IsoformsReceptors, ImmunologicReceptors, ScavengerScavenger Receptors, Class A

Identifiers

PMID10722588
PMCPMC97372
OpenAlexW2104633821

What OpenQuestion holds

Textmetadata
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.