Evidence map›Paper›PMID 32548608›Full record

ArticleBlood2020

Megakaryocyte TGFβ1 partitions erythropoiesis into immature progenitor/stem cells and maturing precursors.

Silvana Di Giandomenico, Pouneh Kermani, Nicole Mollé, Maria Mia Yabut, Ghaith Abu-Zeinah, Thomas Stephens, Nassima Messali, Ryan Schreiner, Fabienne Brenet, Shahin Rafii and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Versatility of megakaryocytes in homeostasis and disease.Blood science (Baltimore, Md.) · 2024
    Review
  8. Immunoregulation role of the erythroid cells.Frontiers in immunology · 2024
    Review
  9. Article
  10. Targeting inflammation in lower-risk MDS.Hematology. American Society of Hematology. Education Program · 2022
    Article
  11. Article
  12. Article
  13. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 2 countries.

Silvana Di GiandomenicoLaboratory of Molecular Hematopoiesis, Hematology and Oncology.
Pouneh KermaniLaboratory of Molecular Hematopoiesis, Hematology and Oncology.
Nicole MolléLaboratory of Molecular Hematopoiesis, Hematology and Oncology.
Maria Mia YabutLaboratory of Molecular Hematopoiesis, Hematology and Oncology.
Ghaith Abu-ZeinahLaboratory of Molecular Hematopoiesis, Hematology and Oncology.
Thomas StephensLaboratory of Molecular Hematopoiesis, Hematology and Oncology.
Nassima MessaliLaboratory of Molecular Hematopoiesis, Hematology and Oncology.
Ryan SchreinerDepartment of Opthalmology and.
Fabienne BrenetLaboratory of Molecular Hematopoiesis, Hematology and Oncology.
Shahin RafiiRegenerative Medicine, Department of Medicine, Weill Cornell Medicine, New York, NY.
Joseph M ScanduraLaboratory of Molecular Hematopoiesis, Hematology and Oncology.
Laboratory of Molecular Genetics · PLCornell University · US

Funding

Molecular and Translational Oncology ResearchT32CA203702 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI BLENIS, JOHN, GIANNAKAKOU, PARASKEVI · 2017 to 2021
$1.4M
NCI NIH HHS T32 CA203702
6 · The paper itself

Abstract

Erythropoietin (EPO) provides the major survival signal to maturing erythroid precursors (EPs) and is essential for terminal erythropoiesis. Nonetheless, progenitor cells can irreversibly commit to an erythroid fate well before EPO acts, risking inefficiency if these progenitors are unneeded to maintain red blood cell (RBC) counts. We identified a new modular organization of erythropoiesis and, for the first time, demonstrate that the pre-EPO module is coupled to late EPO-dependent erythropoiesis by megakaryocyte (Mk) signals. Disrupting megakaryocytic transforming growth factor β1 (Tgfb1) disorganized hematopoiesis by expanding the pre-EPO pool of progenitor cells and consequently triggering significant apoptosis of EPO-dependent EPs. Similarly, pharmacologic blockade of TGFβ signaling in normal mice boosted the pre-EPO module, leading to apoptosis of EPO-sensitive EPs. Subsequent treatment with low-dose EPO triggered robust RBC production in both models. This work reveals modular regulation of erythropoiesis and offers a new strategy for overcoming chronic anemias.

Indexed as

AnimalsApoptosisBone MarrowErythroid Precursor CellsErythropoiesisErythropoietinGene Knockout TechniquesHematopoietic Stem CellsImmunophenotypingMegakaryocyte-Erythroid Progenitor CellsMegakaryocytesMiceMice, Inbred C57BLMice, TransgenicRadiation ChimeraRecombinant ProteinsEPO protein, humanErythropoietinRecombinant ProteinsTgfb1 protein, mouseTransforming Growth Factor beta1

Identifiers

PMID32548608
PMCPMC7453150
OpenAlexW3035356857

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.