Evidence map›Paper›PMID 40012014›Full record

ArticleBritish journal of haematology2025

Iron trapping in macrophages reshapes the homeostasis of the haematopoietic system.

Laura Crisafulli, Margherita Correnti, Elena Gammella, Elisa De Camilli, Matteo Brindisi, Eleonora Palagano, Chiara Milanesi, Gabriele Todisco, Matteo G Della Porta, Cristina Sobacchi and 3 more

Abstract read
In one paragraph

Article in British journal of haematology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Review
  2. Article
  3. The spleen-brain axis in Alzheimer's disease and related dementias: Integrating immune and metabolic regulation.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
    Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. 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

13 authors.

Laura CrisafulliMilan Unit, CNR-IRGB, Milan, Italy.
Margherita CorrentiDepartment of Biomedical Sciences for Health, University of Milan, Milan, Italy.
Elena GammellaDepartment of Biomedical Sciences for Health, University of Milan, Milan, Italy.
Elisa De CamilliDivision of Pathology, IEO, European Institute of Oncology IRCCS, Milan, Italy.
Matteo BrindisiMilan Unit, CNR-IRGB, Milan, Italy.
Eleonora PalaganoIRCCS Humanitas Research Hospital, Milan, Italy.
Chiara MilanesiIRCCS Humanitas Research Hospital, Milan, Italy.
Gabriele TodiscoIRCCS Humanitas Research Hospital, Milan, Italy.
Matteo G Della PortaIRCCS Humanitas Research Hospital, Milan, Italy.
Cristina SobacchiMilan Unit, CNR-IRGB, Milan, Italy.
Gaetano CairoDepartment of Biomedical Sciences for Health, University of Milan, Milan, Italy.
Francesca FicaraMilan Unit, CNR-IRGB, Milan, Italy.ORCID https://orcid.org/0000-0003-1873-1189
Stefania RecalcatiDepartment of Biomedical Sciences for Health, University of Milan, Milan, Italy.

Funding

Fondazione Cariplo GJC21072Ministero dell'Università e della Ricerca
6 · The paper itself

Abstract

Iron is required for key physiological processes, like oxygen transport, energy production and cell proliferation. Body iron homeostasis is regulated by the erythroferrone-hepcidin-ferroportin (FPN) axis, which mainly acts on absorptive duodenal cells and macrophages involved in iron recycling from red blood cell breakdown. In addition to systemic iron regulation, macrophages are also involved in local iron release to neighbouring cells. Similarly, bone marrow (BM)-resident macrophages could represent promptly available local sources of iron for developing haematopoietic cells. To study the impact of macrophage-released iron on BM haematopoietic stem and progenitor cells, we employed mice with targeted deletion of Fpn in the myeloid lineage (Fpn conditional knockout or Fpn-cKO). Fpn-cKO mice develop age-related anaemia and microcytaemia, reduction of BM erythroblasts and preferential megakaryopoiesis at the expenses of erythropoiesis, suggesting that red cells are mostly affected by the lack of myeloid-derived iron delivery. Transferrin receptor 1 surface expression is higher in Fpn-cKO mice than littermate controls in all the BM subpopulation analysed, starting from haematopoietic stem cells, indicating a broad BM sensitivity to lower iron availability. Last, Fpn-cKO mice activate systemic compensatory mechanisms, such as extramedullary haematopoiesis and erythroferrone upregulation, albeit not sufficient to overcome anaemia.

Indexed as

HematopoiesisHomeostasisIronMacrophagesAnimalsCation Transport ProteinsErythropoiesisFerroportinHematopoietic Stem CellsHepcidinsMiceMice, KnockoutReceptors, TransferrinCation Transport ProteinsFerroportinHepcidinsIronReceptors, Transferrinanaemiaanimal modelhaematopoiesisironmacrophagesred cells

Identifiers

PMID40012014
PMCPMC12078876

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.