Evidence map›Paper›PMID 38232308›Full record

ArticleBlood2024

The hepatokine FGL1 regulates hepcidin and iron metabolism during anemia in mice by antagonizing BMP signaling.

Ugo Sardo, Prunelle Perrier, Kevin Cormier, Manon Sotin, Jean Personnaz, Thanina Medjbeur, Aurore Desquesnes, Lisa Cannizzo, Marc Ruiz-Martinez, Julie Thevenin and 8 more

Abstract read
In one paragraph

Article in Blood, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
12.7field-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

20 citing papers in PubMed, 28 citations in OpenAlex.

  1. Thalassaemia.Nature reviews. Disease primers · 2026
    Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Ablation of Hepatocyte Derived-FGL1 Does Not Aggravate Metabolic Dysfunction-Associated Steatotic Liver Disease.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  11. Article
  12. Review
  13. Outline of Iron Metabolism, with Emphasis on Erythroid Cells.Mediterranean journal of hematology and infectious diseases · 2025
    Review
  14. Systemic Iron Metabolism.Advances in experimental medicine and biology · 2025
    Review
  15. Review
  16. Iron-Loading Anemias.Advances in experimental medicine and biology · 2025
    Review
  17. Current Landscape of Hepcidin Therapeutics.Advances in experimental medicine and biology · 2025
    Review
  18. Review
  19. Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 4 institutions in 2 countries.

Ugo SardoInstitut de Recherche en Santé Digestive, Université de Toulouse, INSERM, INRAE, ENVT, Université Toulouse III Paul Sabatier, Toulouse, France.
Prunelle PerrierInstitut de Recherche en Santé Digestive, Université de Toulouse, INSERM, INRAE, ENVT, Université Toulouse III Paul Sabatier, Toulouse, France.
Kevin CormierInstitut de Recherche en Santé Digestive, Université de Toulouse, INSERM, INRAE, ENVT, Université Toulouse III Paul Sabatier, Toulouse, France.
Manon SotinInstitut de Recherche en Santé Digestive, Université de Toulouse, INSERM, INRAE, ENVT, Université Toulouse III Paul Sabatier, Toulouse, France.
Jean PersonnazInstitut de Recherche en Santé Digestive, Université de Toulouse, INSERM, INRAE, ENVT, Université Toulouse III Paul Sabatier, Toulouse, France.ORCID 0000-0001-6447-780X
Thanina MedjbeurInstitut de Recherche en Santé Digestive, Université de Toulouse, INSERM, INRAE, ENVT, Université Toulouse III Paul Sabatier, Toulouse, France.
Aurore DesquesnesInstitut de Recherche en Santé Digestive, Université de Toulouse, INSERM, INRAE, ENVT, Université Toulouse III Paul Sabatier, Toulouse, France.
Lisa CannizzoInstitut de Recherche en Santé Digestive, Université de Toulouse, INSERM, INRAE, ENVT, Université Toulouse III Paul Sabatier, Toulouse, France.
Marc Ruiz-MartinezIcahn School of Medicine Mount Sinai Hospital, New York, NY.
Julie TheveninInstitut de Recherche en Santé Digestive, Université de Toulouse, INSERM, INRAE, ENVT, Université Toulouse III Paul Sabatier, Toulouse, France.ORCID 0009-0004-3462-9947
Benjamin BilloréInstitut de Recherche en Santé Digestive, Université de Toulouse, INSERM, INRAE, ENVT, Université Toulouse III Paul Sabatier, Toulouse, France.
Grace JungDepartment of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA.
Elise AbboudInstitut Cochin, INSERM, Centre National de la Recherche Scientifique, Université de Paris, Paris, France.
Carole PeyssonnauxInstitut Cochin, INSERM, Centre National de la Recherche Scientifique, Université de Paris, Paris, France.
Elizabeta NemethDepartment of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA.ORCID 0000-0002-3477-2397
Yelena Z GinzburgIcahn School of Medicine Mount Sinai Hospital, New York, NY.ORCID 0000-0002-3496-3783
Tomas GanzDepartment of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA.ORCID 0000-0002-2830-5469
Léon KautzInstitut de Recherche en Santé Digestive, Université de Toulouse, INSERM, INRAE, ENVT, Université Toulouse III Paul Sabatier, Toulouse, France.ORCID 0000-0002-2320-0457
Université Toulouse III - Paul Sabatier · FRUniversity of California, Los Angeles · USInserm · FRMount Sinai Hospital · US

Funding

Regulatory Role of Transferrin in Erythropoiesis and Iron MetabolismR01DK095112 · NIDDK · SAINT LOUIS UNIVERSITY · PI Robert E Fleming, Yelena Ginzburg · 2012 to 2026
$5.4M
The Role of Erythroferrone in Regulating Bone Metabolism in Beta-ThalassemiaR01DK107670 · NIDDK · NEW YORK BLOOD CENTER · PI GINZBURG, YELENA, YUEN, TONY · 2015 to 2025
$4.5M
MECHANISM OF ACTION OF ERYTHROFERRONE AND PATHOLOGICAL IMPLICATIONSR01DK126680 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI GANZ, TOMAS · 2020 to 2024
$2.6M
NIDDK NIH HHS R01 DK095112NIDDK NIH HHS R01 DK107670NIDDK NIH HHS R01 DK126680
6 · The paper itself

Abstract

abstractAs a functional component of erythrocyte hemoglobin, iron is essential for oxygen delivery to all tissues in the body. The liver-derived peptide hepcidin is the master regulator of iron homeostasis. During anemia, the erythroid hormone erythroferrone regulates hepcidin synthesis to ensure the adequate supply of iron to the bone marrow for red blood cell production. However, mounting evidence suggested that another factor may exert a similar function. We identified the hepatokine fibrinogen-like 1 (FGL1) as a previously undescribed suppressor of hepcidin that is induced in the liver in response to hypoxia during the recovery from anemia, and in thalassemic mice. We demonstrated that FGL1 is a potent suppressor of hepcidin in vitro and in vivo. Deletion of Fgl1 in mice results in higher hepcidin levels at baseline and after bleeding. FGL1 exerts its activity by directly binding to bone morphogenetic protein 6 (BMP6), thereby inhibiting the canonical BMP-SMAD signaling cascade that controls hepcidin transcription.

Indexed as

AnemiaHepcidinsAnimalsBone Morphogenetic Protein 6HomeostasisIronLiverMiceBone Morphogenetic Protein 6HepcidinsIron

Identifiers

PMID38232308
PMCPMC11103088
OpenAlexW4390935909

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.