Evidence map›Paper›PMID 20184753›Full record

ArticleBMC microbiology2010

Modulation of iron homeostasis in macrophages by bacterial intracellular pathogens.

Xin Pan, Batcha Tamilselvam, Eric J Hansen, Simon Daefler

Open access · goldAbstract read
In one paragraph

Article in BMC microbiology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

49 citing papers in PubMed, 70 citations in OpenAlex.

  1. Genomic Insights into Vector-Pathogen Adaptation inPathogens (Basel, Switzerland) · 2025
    Article
  2. Article
  3. Review
  4. Frontiers in microbiology · 2023
    Article
  5. Article
  6. Article
  7. Article
  8. Iron Reduction inInternational journal of molecular sciences · 2022
    Article
  9. Airway Epithelial Cells Differentially Adapt Their Iron Metabolism to Infection WithFrontiers in cellular and infection microbiology · 2022
    Article
  10. PAMPs ofFrontiers in immunology · 2022
    Article
  11. Chimeric Protein IPathVaccines · 2021
    Article
  12. Perls' Prussian Blue Stains of Lung Tissue, Bronchoalveolar Lavage, and Sputum.Journal of environmental pathology, toxicology and oncology : official organ of the International Society for Environmental Toxicology and Cancer · 2021
    Article
  13. Review
  14. Control ofMicroorganisms · 2020
    Review
  15. Review
  16. Review
  17. Article
  18. Article
  19. Structure and Metal Binding Properties ofJournal of bacteriology · 2019
    Article
  20. 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

4 authors at 2 institutions in 1 country.

Xin PanMount Sinai School of Medicine, One Gustave Levy Place, New York, NY 10570, USA.
Batcha Tamilselvam
Eric J Hansen
Simon Daefler
Icahn School of Medicine at Mount Sinai · USUniversity of Texas Health Science Center at Dallas · US

Funding

Molecular Biology of Francisella tularensis VirulenceP01AI055637 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI NORGARD, MICHAEL V · 2003 to 2007
$8.5M
NIAID NIH HHS P0AI55637
6 · The paper itself

Abstract

backgroundIntracellular bacterial pathogens depend on acquisition of iron for their success as pathogens. The host cell requires iron as an essential component for cellular functions that include innate immune defense mechanisms. The transferrin receptor TfR1 plays an important part for delivering iron to the host cell during infection. Its expression can be modulated by infection, but its essentiality for bacterial intracellular survival has not been directly investigated.

resultsWe identified two distinct iron-handling scenarios for two different bacterial pathogens. Francisella tularensis drives an active iron acquisition program via the TfR1 pathway program with induction of ferrireductase (Steap3), iron membrane transporter Dmt1, and iron regulatory proteins IRP1 and IRP2, which is associated with a sustained increase of the labile iron pool inside the macrophage. Expression of TfR1 is critical for Francisella's intracellular proliferation. This contrasts with infection of macrophages by wild-type Salmonella typhimurium, which does not require expression of TfR1 for successful intracellular survival. Macrophages infected with Salmonella lack significant induction of Dmt1, Steap3, and IRP1, and maintain their labile iron pool at normal levels.

conclusionThe distinction between two different phenotypes of iron utilization by intracellular pathogens will allow further characterization and understanding of host-cell iron metabolism and its modulation by intracellular bacteria.

Indexed as

AnimalsCell Growth ProcessesCell LineCytoplasmic VesiclesFrancisella tularensisGene Expression RegulationHomeostasisIntracellular SpaceIronMacrophagesMetabolic Networks and PathwaysMiceReceptors, TransferrinSalmonella typhimuriumUp-RegulationIronReceptors, TransferrinTfrc protein, mouse

Identifiers

PMID20184753
PMCPMC2838877
OpenAlexW2121253747

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.