Evidence map›Paper›PMID 30996139›Full record

ArticleJCI insight2019

Classical and intermediate monocytes scavenge non-transferrin-bound iron and damaged erythrocytes.

David Haschka, Verena Petzer, Florian Kocher, Christoph Tschurtschenthaler, Benedikt Schaefer, Markus Seifert, Sieghart Sopper, Thomas Sonnweber, Clemens Feistritzer, Tara L Arvedson and 5 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed, 30 citations in OpenAlex.

  1. Particles exposures and sarcoidosis.Sarcoidosis, vasculitis, and diffuse lung diseases : official journal of WASOG · 2025
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
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  12. On Iron Metabolism and Its Regulation.International journal of molecular sciences · 2021
    Review
  13. Distinct Effects ofInternational journal of molecular sciences · 2021
    Article
  14. Article
  15. Article
  16. Article
  17. Macrophages: key players in erythrocyte turnover.Hematology, transfusion and cell therapy
    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

15 authors at 3 institutions in 3 countries.

David HaschkaDepartment of Internal Medicine II.
Verena PetzerDepartment of Internal Medicine II.
Florian KocherDepartment of Internal Medicine V, and.
Christoph TschurtschenthalerDepartment of Internal Medicine II.
Benedikt SchaeferDepartment of Internal Medicine I, Medical University of Innsbruck, Innsbruck, Austria.
Markus SeifertDepartment of Internal Medicine II.
Sieghart SopperDepartment of Internal Medicine V, and.
Thomas SonnweberDepartment of Internal Medicine II.
Clemens FeistritzerDepartment of Internal Medicine V, and.
Tara L ArvedsonDepartment of Oncology, Amgen Inc., Thousand Oaks, California, USA.
Heinz ZollerDepartment of Internal Medicine I, Medical University of Innsbruck, Innsbruck, Austria.
Reinhard StauderDepartment of Internal Medicine V, and.
Igor TheurlDepartment of Internal Medicine II.
Guenter WeissDepartment of Internal Medicine II.
Piotr TymoszukDepartment of Internal Medicine II.
Institute of Ismaili Studies · GBInnsbruck Medical University · ATAmgen (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myelomonocytic cells are critically involved in iron turnover as aged RBC recyclers. Human monocytes are divided in 3 subpopulations of classical, intermediate, and nonclassical cells, differing in inflammatory and migratory phenotype. Their functions in iron homeostasis are, however, unclear. Here, we asked whether the functional diversity of monocyte subsets translates into differences in handling physiological and pathological iron species. By microarray data analysis and flow cytometry we identified a set of iron-related genes and proteins upregulated in classical and, in part, intermediate monocytes. These included the iron exporter ferroportin (FPN1), ferritin, transferrin receptor, putative transporters of non-transferrin-bound iron (NTBI), and receptors for damaged erythrocytes. Consequently, classical monocytes displayed superior scavenging capabilities of potentially toxic NTBI, which were augmented by blocking iron export via hepcidin. The same subset and, to a lesser extent, the intermediate population, efficiently cleared damaged erythrocytes in vitro and mediated erythrophagocytosis in vivo in healthy volunteers and patients having received blood transfusions. To summarize, our data underline the physiologically important function of the classical and intermediate subset in clearing NTBI and damaged RBCs. As such, these cells may play a nonnegligible role in iron homeostasis and limit iron toxicity in iron overload conditions.

Indexed as

AdultAgedAged, 80 and overCation Transport ProteinsErythrocytesErythrocyte TransfusionFemaleFerroportinFlow CytometryGene Expression ProfilingHealthy VolunteersHomeostasisHumansIronIron OverloadMaleCation Transport ProteinsFerroportinIronTransferrinImmunologyInnate immunityMetabolismMonocytes

Identifiers

PMID30996139
PMCPMC6538345
OpenAlexW2938935447

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.