Evidence map›Paper›PMID 32350523›Full record

ArticleBlood2020

Epo receptor signaling in macrophages alters the splenic niche to promote erythroid differentiation.

Yuanting Chen, Jie Xiang, Fenghua Qian, Bastihalli T Diwakar, Baiye Ruan, Siyang Hao, K Sandeep Prabhu, Robert F Paulson

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 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

26 citing papers in PubMed, 53 citations in OpenAlex.

  1. Redox Modulation of Erythropoiesis by Selenoproteins.Biological trace element research · 2026
    Review
  2. Macrophages in Hematopoiesis and Related Blood Diseases.Genomics, proteomics & bioinformatics · 2025
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Editorial: Stress erythropoiesis.Frontiers in physiology · 2023
    Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Review
  20. 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

8 authors at 2 institutions in 2 countries.

Yuanting ChenGraduate Program in Molecular, Cellular, and Integrative Biosciences, Huck Institutes of the Life Sciences.
Jie XiangGraduate Program in Molecular, Cellular, and Integrative Biosciences, Huck Institutes of the Life Sciences.
Fenghua QianGraduate Program in Pathobiology.
Bastihalli T DiwakarDepartment of Veterinary and Biomedical Sciences, and.
Baiye RuanGraduate Program in Pathobiology.
Siyang HaoGraduate Program in Molecular, Cellular, and Integrative Biosciences, Huck Institutes of the Life Sciences.
K Sandeep PrabhuGraduate Program in Molecular, Cellular, and Integrative Biosciences, Huck Institutes of the Life Sciences.
Robert F PaulsonGraduate Program in Molecular, Cellular, and Integrative Biosciences, Huck Institutes of the Life Sciences.
Pennsylvania State University · USUniversity of Veterinary Science · MM

Funding

The BMP4 dependent stress erythropoiesis pathway in short-term radioprotectionR01DK080040 · NIDDK · PENNSYLVANIA STATE UNIVERSITY, THE · PI PAULSON, ROBERT FRANK · 2009 to 2017
$2.6M
Cellular Selenium Status and PGJ2 Metabolism (PA-17-078 supplement 2017)R01DK077152 · NIDDK · PENNSYLVANIA STATE UNIVERSITY, THE · PI PRABHU, KUMBLE SANDEEP · 2008 to 2018
$2.5M
Selenium, Selenoproteins, and Stress ErythropoiesisR01DK119865 · NIDDK · PENNSYLVANIA STATE UNIVERSITY, THE · PI PAULSON, ROBERT FRANK, PRABHU, KUMBLE SANDEEP · 2019 to 2021
$1.1M
NIDDK NIH HHS R01 DK077152NIDDK NIH HHS R01 DK080040NIDDK NIH HHS R01 DK119865
6 · The paper itself

Abstract

Anemic stress induces stress erythropoiesis, which rapidly generates new erythrocytes to restore tissue oxygenation. Stress erythropoiesis is best understood in mice where it is extramedullary and occurs primarily in the spleen. However, both human and mouse stress erythropoiesis use signals and progenitor cells that are distinct from steady-state erythropoiesis. Immature stress erythroid progenitors (SEPs) are derived from short-term hematopoietic stem cells. Although the SEPs are capable of self-renewal, they are erythroid restricted. Inflammation and anemic stress induce the rapid proliferation of SEPs, but they do not differentiate until serum erythropoietin (Epo) levels increase. Here we show that rather than directly regulating SEPs, Epo promotes this transition from proliferation to differentiation by acting on macrophages in the splenic niche. During the proliferative stage, macrophages produce canonical Wnt ligands that promote proliferation and inhibit differentiation. Epo/Stat5-dependent signaling induces the production of bioactive lipid mediators in macrophages. Increased production of prostaglandin J2 (PGJ2) activates peroxisome proliferator-activated receptor γ (PPARγ)-dependent repression of Wnt expression, whereas increased production of prostaglandin E2 (PGE2) promotes the differentiation of SEPs.

Indexed as

Cell DifferentiationSignal TransductionStem Cell NicheAnimalsDinoprostoneErythroid CellsHumansMacrophagesMiceMice, TransgenicPPAR gammaProstaglandin D2Receptors, ErythropoietinSpleenSTAT5 Transcription Factor9-deoxy-delta-9-prostaglandin D2DinoprostonePPAR gammaPparg protein, mouseProstaglandin D2Receptors, ErythropoietinSTAT5 Transcription Factor

Identifiers

PMID32350523
PMCPMC7357191
OpenAlexW3022239962

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.