Evidence map›Paper›PMID 18680715›Full record

ArticleCell metabolism2008

The hepcidin-binding site on ferroportin is evolutionarily conserved.

Ivana De Domenico, Elizabeta Nemeth, Jenifer M Nelson, John D Phillips, Richard S Ajioka, Michael S Kay, James P Kushner, Tomas Ganz, Diane M Ward, Jerry Kaplan

RetractedOpen access · bronzeAbstract readRetracted Publication
In one paragraph

Article in Cell metabolism, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 56 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 1 pooled it
12.3field-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

56 citing papers in PubMed, 1 synthesis or guideline pooled it, 127 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Identification of Antibacterial Activity ofFrontiers in microbiology · 2022
    Article
  5. Reduced iron export associated with hepcidin resistance can explain the iron overload spectrum in ferroportin disease.Liver international : official journal of the International Association for the Study of the Liver · 2020
    Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Ironing out Ferroportin.Cell metabolism · 2015
    Review
  11. Review
  12. Article
  13. Iron-refractory iron deficiency anemia.Turkish journal of haematology : official journal of Turkish Society of Haematology · 2015
    Article
  14. Low intracellular iron increases the stability of matriptase-2.The Journal of biological chemistry · 2015
    Article
  15. Review
  16. A novel model for brain iron uptake: introducing the concept of regulation.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2015
    Article
  17. Article
  18. Article
  19. Ceruloplasmin-ferroportin system of iron traffic in vertebrates.World journal of biological chemistry · 2014
    Review
  20. Hepcidin in neoplastic disease.Journal of medicine and life · 2013
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Ivana De DomenicoDepartment of Pathology, School of Medicine, University of Utah, Salt Lake City, UT 84132, USA.
Elizabeta Nemeth
Jenifer M Nelson
John D Phillips
Richard S Ajioka
Michael S Kay
James P Kushner
Tomas Ganz
Diane M Ward
Jerry Kaplan
University of Utah · USUniversity of California, Los Angeles · US

Funding

X-ray Cryst. CoreP50GM082545 · NIGMS · UNIVERSITY OF UTAH · PI HOPE, THOMAS · 2007 to 2018
$51.1M
Crystallography CoreP30DK072437 · NIDDK · UNIVERSITY OF UTAH · PI KAPLAN, JERRY · 2005 to 2010
$4.0M
Mechanism and Regulation of Iron Export by FerroportinR01DK070947 · NIDDK · UNIVERSITY OF UTAH · PI KAPLAN, JERRY · 2005 to 2014
$3.7M
PORPHYRIN BIOSYNTHESIS IN NORMAL AND DISEASE STATESR01DK020503 · NIDDK · UNIVERSITY OF UTAH · PI PARKER, CHARLES J, PHILLIPS, JOHN DEARBORN · 1986 to 2012
$3.3M
NIDDK NIH HHS DK 070947NIDDK NIH HHS P30 DK072437NIDDK NIH HHS R01 DK020503NIDDK NIH HHS R01 DK070947NIDDK NIH HHS SP30DK072437NIGMS NIH HHS GM 082545NIGMS NIH HHS P50 GM082545
6 · The paper itself

Abstract

Mammalian iron homeostasis is regulated by the interaction of the liver-produced peptide hepcidin and its receptor, the iron transporter ferroportin. Hepcidin binds to ferroportin resulting in degradation of ferroportin and decreased cellular iron export. We identify the hepcidin-binding domain (HBD) on ferroportin and show that a synthetic 19 amino acid peptide corresponding to the HBD recapitulates the characteristics and specificity of hepcidin binding to cell-surface ferroportin. The binding of mammalian hepcidin to ferroportin or the HBD shows an unusual temperature dependency with an increased rate of dissociation at temperatures below 15 degrees C. The increased rate of dissociation is due to temperature- dependent changes in hepcidin structure. In contrast, hepcidin from poikilothermic vertebrates, such as fish or frogs, binds the HBD in a temperature-independent fashion. The affinity of hepcidin for the HBD permits a rapid, sensitive assay of hepcidin from all species and yields insights into the evolution of hepcidin.

Indexed as

Amino Acid SequenceAnimalsAntimicrobial Cationic PeptidesAnuraBinding SitesBody TemperatureCation Transport ProteinsCell LineConserved SequenceEvolution, MolecularFerroportinFishesHepcidinsHumansIronLiverAntimicrobial Cationic PeptidesCation Transport ProteinsFerroportinHAMP protein, humanHepcidinsIronPeptides

Identifiers

PMID18680715
PMCPMC2660598
OpenAlexW1482134942

What OpenQuestion holds

Textmetadata
LicenceTDM
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.