Evidence map›Paper›PMID 21886823›Full record

ArticlePloS one2011

Iron uptake mediated by binding of H-ferritin to the TIM-2 receptor in mouse cells.

Jian Han, William E Seaman, Xiumin Di, Wei Wang, Mark Willingham, Frank M Torti, Suzy V Torti

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

54 citing papers in PubMed, 88 citations in OpenAlex.

  1. Iron Homeostasis and Liver Diseases.Journal of cellular and molecular medicine · 2026
    Review
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Mechanisms controlling cellular and systemic iron homeostasis.Nature reviews. Molecular cell biology · 2024
    Review
  11. Article
  12. A novel view of ferritin in cancer.Biochimica et biophysica acta. Reviews on cancer · 2023
    Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Observational
  18. Article
  19. Iron Homeostasis and Metabolism: Two Sides of a Coin.Advances in experimental medicine and biology · 2021
    Review
  20. Iron and Cancer: 2020 Vision.Cancer research · 2020
    Review
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 3 institutions in 1 country.

Jian HanDepartment of Biology, North Carolina Agricultural and Technical State University, Greensboro, North Carolina, United States of America.
William E Seaman
Xiumin Di
Wei Wang
Mark Willingham
Frank M Torti
Suzy V Torti
Wake Forest University · USNorth Carolina Agricultural and Technical State University · USSan Francisco VA Medical Center · US

Funding

Ferritin, Iron Homeostasis and Cellular StressR37DK042412 · NIDDK · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI TORTI, FRANK M. · 2001 to 2011
$3.8M
Role of the Tim-2 Receptor in Immunity and AutoimmunityR01AI061164 · NIAID · NORTHERN CALIFORNIA INSTITUTE RES &EDUC · PI SEAMAN, WILLIAM E · 2005 to 2008
$1.5M
Ferritin and Kininogen InteractionR01DK071892 · NIDDK · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI TORTI, SUZY V · 2007 to 2011
$1.3M
NIAID NIH HHS R01 AI061164NIDDK NIH HHS R01 DK071892NIDDK NIH HHS R37 DK042412NIDDK NIH HHS R37 DK42412
6 · The paper itself

Abstract

Ferritin binds specifically and saturably to a variety of cell types, and recently several ferritin receptors have been cloned. TIM-2 is a specific receptor for H ferritin (HFt) in the mouse. TIM-2 is a member of the T cell immunoglobulin and mucin domain containing (TIM) protein family and plays an important role in immunity. The expression of TIM-2 outside of the immune system indicates that this receptor may have broader roles. We tested whether ferritin binding to TIM-2 can serve as an iron delivery mechanism. TIM-2 was transfected into normal (TCMK-1) mouse kidney cells, where it was appropriately expressed on the cell surface. HFt was labeled with (55)Fe and (55)Fe-HFt was incubated with TIM-2 positive cells or controls. (55)Fe-HFt uptake was observed only in TIM-2 positive cells. HFt uptake was also seen in A20 B cells, which express endogenous TIM-2. TIM-2 levels were not increased by iron chelation. Uptake of (55)Fe-HFt was specific and temperature-dependent. HFt taken up by TIM-2 positive cells transited through the endosome and eventually entered a lysosomal compartment, distinguishing the HFt pathway from that of transferrin, the classical vehicle for cellular iron delivery. Iron delivered following binding of HFt to TIM-2 entered the cytosol and became metabolically available, resulting in increased levels of endogenous intracellular ferritin. We conclude that TIM-2 can function as an iron uptake pathway.

Indexed as

AnimalsApoferritinsBiological TransportEndosomesIronKidneyLysosomesMembrane ProteinsMiceProtein BindingTransfectionApoferritinsIronMembrane ProteinsTimd2 protein, mouse

Identifiers

PMID21886823
PMCPMC3158792
OpenAlexW1970672739

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.