Evidence map›Paper›PMID 22019886›Full record

ArticleNature medicine2011

Polymeric IgA1 controls erythroblast proliferation and accelerates erythropoiesis recovery in anemia.

Séverine Coulon, Michaël Dussiot, Damien Grapton, Thiago Trovati Maciel, Pamella Huey Mei Wang, Celine Callens, Meetu Kaushik Tiwari, Saurabh Agarwal, Aurelie Fricot, Julie Vandekerckhove and 16 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature medicine, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

40 citing papers in PubMed, 68 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Review
  5. Activation of Intestinal HIF2α Ameliorates Iron-Refractory Anemia.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  6. Mechanisms controlling cellular and systemic iron homeostasis.Nature reviews. Molecular cell biology · 2024
    Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Transferrin Receptors in Erythropoiesis.International journal of molecular sciences · 2020
    Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Review
  19. New insights into the pathogenesis of IgA nephropathy.Pediatric nephrology (Berlin, Germany) · 2018
    Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

26 authors at 7 institutions in 2 countries.

Séverine CoulonCentre National de la Recherche Scientifique (CNRS) Unité Mixte Recherche (UMR) 8147, Université Paris Descartes, Faculté de Médecine, Hôpital Necker, Paris, France.
Michaël Dussiot
Damien Grapton
Thiago Trovati Maciel
Pamella Huey Mei Wang
Celine Callens
Meetu Kaushik Tiwari
Saurabh Agarwal
Aurelie Fricot
Julie Vandekerckhove
Houda Tamouza
Yael Zermati
Jean-Antoine Ribeil
Kamel Djedaini
Zeliha Oruc
Virginie Pascal
Geneviève Courtois
Bertrand Arnulf
Marie-Alexandra Alyanakian
Patrick Mayeux
Tomas Leanderson
Marc Benhamou
Michel Cogné
Renato C Monteiro
Olivier Hermine
Ivan C Moura
Université Paris Cité · FRCentre National de la Recherche Scientifique · FRInserm · FRHôpital Necker-Enfants Malades · FRUniversité de Limoges · FRInstitut Cochin · FRLund University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Anemia because of insufficient production of and/or response to erythropoietin (Epo) is a major complication of chronic kidney disease and cancer. The mechanisms modulating the sensitivity of erythroblasts to Epo remain poorly understood. We show that, when cultured with Epo at suboptimal concentrations, the growth and clonogenic potential of erythroblasts was rescued by transferrin receptor 1 (TfR1)-bound polymeric IgA1 (pIgA1). Under homeostatic conditions, erythroblast numbers were increased in mice expressing human IgA1 compared to control mice. Hypoxic stress of these mice led to increased amounts of pIgA1 and erythroblast expansion. Expression of human IgA1 or treatment of wild-type mice with the TfR1 ligands pIgA1 or iron-loaded transferrin (Fe-Tf) accelerated recovery from acute anemia. TfR1 engagement by either pIgA1 or Fe-Tf increased cell sensitivity to Epo by inducing activation of mitogen-activated protein kinase (MAPK) and phosphatidylinositol 3-kinase (PI3K) signaling pathways. These cellular responses were mediated through the TfR1-internalization motif, YXXΦ. Our results show that pIgA1 and TfR1 are positive regulators of erythropoiesis in both physiological and pathological situations. Targeting this pathway may provide alternate approaches to the treatment of ineffective erythropoiesis and anemia.

Indexed as

Cell ProliferationAnemiaAnimalsCells, CulturedErythroblastsErythropoiesisErythropoietinHumansHypoxiaImmunoglobulin AMiceMice, Inbred NODMice, SCIDMice, TransgenicMitogen-Activated Protein KinasesPhosphatidylinositol 3-KinasesErythropoietinholotransferrinImmunoglobulin AMitogen-Activated Protein KinasesPhosphatidylinositol 3-KinasesReceptors, TransferrinTransferrin

Identifiers

PMID22019886
OpenAlexW1975602859

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.