Evidence map›Paper›PMID 18586980›Full record

ArticleJournal of leukocyte biology2008

The iron export protein ferroportin 1 is differentially expressed in mouse macrophage populations and is present in the mycobacterial-containing phagosome.

Kristopher E Van Zandt, Fatoumata B Sow, William C Florence, Bruce S Zwilling, Abhay R Satoskar, Larry S Schlesinger, William P Lafuse

Open access · bronzeAbstract read
In one paragraph

Article in Journal of leukocyte biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

40 citing papers in PubMed, 72 citations in OpenAlex.

  1. Article
  2. Binding of MAP3773c Protein ofInternational journal of molecular sciences · 2024
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  3. Article
  4. Offense and Defense in Granulomatous Inflammation Disease.Frontiers in cellular and infection microbiology · 2022
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Frontiers in cellular and infection microbiology · 2017
    Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Review
  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

7 authors at 2 institutions in 1 country.

Kristopher E Van ZandtDepartment of Microbiology, The Ohio State University, 333 W. 10th Ave., Columbus, OH 43210, USA.
Fatoumata B Sow
William C Florence
Bruce S Zwilling
Abhay R Satoskar
Larry S Schlesinger
William P Lafuse
The Ohio State University · USInterface (United States) · US

Funding

REGULATION OF NRAMP1 MEDIATED IRON TRANSPORTR01DK057667 · NIDDK · OHIO STATE UNIVERSITY · PI ZWILLING, BRUCE S · 2000 to 2004
$1.4M
INHIBITION OF IFN GAMMA SIGNALING BY MYCOBACTERIAR01AI045673 · NIAID · OHIO STATE UNIVERSITY · PI LAFUSE, WILLIAM P · 2001 to 2004
$1.0M
NIAID NIH HHS AI45673NIAID NIH HHS R01 AI045673NIDDK NIH HHS DK57667NIDDK NIH HHS R01 DK057667
6 · The paper itself

Abstract

Intracellular pathogens, including Mycobacterium tuberculosis, obtain iron from the host for their survival. Ferroportin 1 (FPN1; SLC40A1) is the sole iron exporter from mammalian cells and is expressed in the duodenum and macrophages. In the present study, we show that FPN1 mRNA levels in the mouse macrophage cell line RAW264.7 are synergistically induced by treatment with live or gamma-irradiated M. tuberculosis and IFN-gamma. FPN1 mRNA levels were also induced by Mycobacterium avium and IFN-gamma in RAW264.7 cells and the mouse alveolar macrophage cell line AMJ2-C8. Treatment of mouse resident peritoneal macrophages with M. tuberculosis and IFN-gamma resulted in a sixfold increase in FPN1 mRNA expression. In contrast, M. tuberculosis and IFN-gamma inhibited FPN1 mRNA expression in bone marrow-derived macrophages and lung macrophages, which have high basal levels of FPN1 mRNA expression. Using confocal microscopy, FPN1 protein localized rapidly to M. tuberculosis phagosomes after infection in RAW264.7 macrophages. In RAW264.7 cells expressing wild-type natural resistance-associated macrophage protein 1 (Nramp1(Gly169)), FPN1 and Nramp1 partially colocalized in late endosomes/lysosomes prior to infection. After 2 h of infection, Nramp1 and FPN1 were present in M. tuberculosis phagosomes. Our studies provide evidence for transcriptional regulation of FPN1 by pathogenic mycobacteria and IFN-gamma, which is dependent on the macrophage type. The trafficking of FPN1 to the M. tuberculosis phagosome suggests that it is involved in regulating iron availability to the mycobacteria in this locale.

Indexed as

AnimalsBlotting, WesternBone MarrowCation Transport ProteinsCells, CulturedEndosomesFerroportinFluorescent Antibody TechniqueGene Expression RegulationImmunity, InnateInterferon-gammaIronLungLysosomesMacrophages, AlveolarMacrophages, PeritonealCation Transport ProteinsFerroportinInterferon-gammaIronNatural Resistance-associated Macrophage Protein 1

Identifiers

PMID18586980
PMCPMC2516892
OpenAlexW2107596308

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.