Evidence map›Paper›PMID 25608563›Full record

ArticleBlood2015

In vitro culture of stress erythroid progenitors identifies distinct progenitor populations and analogous human progenitors.

Jie Xiang, Dai-Chen Wu, Yuanting Chen, Robert F Paulson

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

60 citing papers in PubMed, 82 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Macrophages in Hematopoiesis and Related Blood Diseases.Genomics, proteomics & bioinformatics · 2025
    Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Fetal Hemoglobin Decrease During Voxelotor Treatment.European journal of haematology · 2025
    Article
  12. Article
  13. Review
  14. Article
  15. Lung Epithelium Releases Growth Differentiation Factor 15 in Response to Pathogen-mediated Injury.American journal of respiratory cell and molecular biology · 2024
    Article
  16. Review
  17. Article
  18. Immunoregulation role of the erythroid cells.Frontiers in immunology · 2024
    Review
  19. Article
  20. Article
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

4 authors at 1 institution in 1 country.

Jie XiangGraduate Program in Molecular, Cellular and Integrative Biosciences.
Dai-Chen WuGraduate Program in Biochemistry, Microbiology and Molecular Biology, and.
Yuanting ChenGraduate Program in Molecular, Cellular and Integrative Biosciences.
Robert F PaulsonGraduate Program in Molecular, Cellular and Integrative Biosciences, Graduate Program in Biochemistry, Microbiology and Molecular Biology, and Center for Molecular Immunology and Infectious Disease, Department of Veterinary and Biomedical Sciences, The Pennsylvania State University, University Park, PA.
Pennsylvania State University · US

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
NIDDK NIH HHS R01 DK080040NIDDK NIH HHS R01DK080040
6 · The paper itself

Abstract

Tissue hypoxia induces a systemic response designed to increase oxygen delivery to tissues. One component of this response is increased erythropoiesis. Steady-state erythropoiesis is primarily homeostatic, producing new erythrocytes to replace old erythrocytes removed from circulation by the spleen. In response to anemia, the situation is different. New erythrocytes must be rapidly made to increase hemoglobin levels. At these times, stress erythropoiesis predominates. Stress erythropoiesis is best characterized in the mouse, where it is extramedullary and utilizes progenitors and signals that are distinct from steady-state erythropoiesis. In this report, we use an in vitro culture system that recapitulates the in vivo development of stress erythroid progenitors. We identify cell-surface markers that delineate a series of stress erythroid progenitors with increasing maturity. In addition, we use this in vitro culture system to expand human stress erythroid progenitor cells that express analogous cell-surface markers. Consistent with previous suggestions that human stress erythropoiesis is similar to fetal erythropoiesis, we demonstrate that human stress erythroid progenitors express fetal hemoglobin upon differentiation. These data demonstrate that similar to murine bone marrow, human bone marrow contains cells that can generate BMP4-dependent stress erythroid burst-forming units when cultured under stress erythropoiesis conditions.

Indexed as

AC133 AntigenAnemiaAnimalsAntigens, CDAntigens, CD34Bone Marrow TransplantationColony-Forming Units AssayErythroid Precursor CellsErythropoiesisErythropoietingamma-GlobinsGlycoproteinsHemoglobinsHumansHypoxiaIn Vitro TechniquesAC133 AntigenAntigens, CDAntigens, CD34EPO protein, humanErythropoietingamma-GlobinsGlycoproteinsHemoglobinsOxygenPeptides

Identifiers

PMID25608563
PMCPMC4357585
OpenAlexW2011228037

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.