Evidence map›Paper›PMID 26028528›Full record

ArticleStem cell reports2015

Bmi-1 Regulates Extensive Erythroid Self-Renewal.

Ah Ram Kim, Jayme L Olsen, Samantha J England, Yu-Shan Huang, Katherine H Fegan, Luis F Delgadillo, Kathleen E McGrath, Paul D Kingsley, Richard E Waugh, James Palis

Abstract read
In one paragraph

Article in Stem cell reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
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

17 citing papers in PubMed.

  1. Dissecting polycomb complexes for enhanced fetal hemoglobin production.bioRxiv : the preprint server for biology · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. BMI1 enables extensive expansion of functional erythroblasts from human peripheral blood mononuclear cells.Molecular therapy : the journal of the American Society of Gene Therapy · 2021
    Article
  9. Bmi1 Maintains the Self-Renewal Property of Innate-like B Lymphocytes.Journal of immunology (Baltimore, Md. : 1950) · 2020
    Article
  10. Article
  11. Article
  12. Article
  13. Revealing nascent proteomics in signaling pathways and cell differentiation.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  14. Review
  15. Review
  16. Development and differentiation of the erythroid lineage in mammals.Developmental and comparative immunology · 2016
    Review
  17. 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

10 authors.

Ah Ram KimCenter for Pediatric Biomedical Research, Department of Pediatrics, University of Rochester Medical Center, Rochester, NY 14642, USA; Department of Biomedical Genetics, University of Rochester Medical Center, Rochester, NY 14642, USA.
Jayme L OlsenCenter for Pediatric Biomedical Research, Department of Pediatrics, University of Rochester Medical Center, Rochester, NY 14642, USA; Department of Biomedical Genetics, University of Rochester Medical Center, Rochester, NY 14642, USA.
Samantha J EnglandDepartment of Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada.
Yu-Shan HuangCenter for Pediatric Biomedical Research, Department of Pediatrics, University of Rochester Medical Center, Rochester, NY 14642, USA; Department of Biomedical Genetics, University of Rochester Medical Center, Rochester, NY 14642, USA.
Katherine H FeganCenter for Pediatric Biomedical Research, Department of Pediatrics, University of Rochester Medical Center, Rochester, NY 14642, USA.
Luis F DelgadilloDepartment of Biomedical Engineering, University of Rochester, Rochester, NY 14611, USA.
Kathleen E McGrathCenter for Pediatric Biomedical Research, Department of Pediatrics, University of Rochester Medical Center, Rochester, NY 14642, USA.
Paul D KingsleyCenter for Pediatric Biomedical Research, Department of Pediatrics, University of Rochester Medical Center, Rochester, NY 14642, USA.
Richard E WaughDepartment of Biomedical Engineering, University of Rochester, Rochester, NY 14611, USA.
James PalisCenter for Pediatric Biomedical Research, Department of Pediatrics, University of Rochester Medical Center, Rochester, NY 14642, USA. Electronic address: james_palis@urmc.rochester.edu.

Funding

The University of Rochester's Clinical and Translational Science InstituteUL1TR000042 · NCATS · UNIVERSITY OF ROCHESTER · PI BENNETT, NANCY M, KIEBURTZ, KARL D. · 2012 to 2015
$14.4M
Embryonic Stem Cell-Derived Platelets as Cellular TherapeuticsU01HL099656 · NHLBI · CHILDREN'S HOSP OF PHILADELPHIA · PI PONCZ, MORTIMER · 2009 to 2015
$8.6M
NCATS NIH HHS UL1 TR000042NCATS NIH HHS UL1TR000042NHLBI NIH HHS U01 HL099656NHLBI NIH HHS U01HL099656
6 · The paper itself

Abstract

Red blood cells (RBCs), responsible for oxygen delivery and carbon dioxide exchange, are essential for our well-being. Alternative RBC sources are needed to meet the increased demand for RBC transfusions projected to occur as our population ages. We previously have discovered that erythroblasts derived from the early mouse embryo can self-renew extensively ex vivo for many months. To better understand the mechanisms regulating extensive erythroid self-renewal, global gene expression data sets from self-renewing and differentiating erythroblasts were analyzed and revealed the differential expression of Bmi-1. Bmi-1 overexpression conferred extensive self-renewal capacity upon adult bone-marrow-derived self-renewing erythroblasts, which normally have limited proliferative potential. Importantly, Bmi-1 transduction did not interfere with the ability of extensively self-renewing erythroblasts (ESREs) to terminally mature either in vitro or in vivo. Bmi-1-induced ESREs can serve to generate in vitro models of erythroid-intrinsic disorders and ultimately may serve as a source of cultured RBCs for transfusion therapy.

Indexed as

AnimalsCell ProliferationDexamethasoneErythroblastsErythropoietinMiceMice, Inbred C57BLMice, Inbred ICRMice, Inbred NODMice, KnockoutMice, SCIDMice, TransgenicPolycomb Repressive Complex 1Proto-Oncogene ProteinsRNA InterferenceRNA, Small InterferingBmi1 protein, mouseDexamethasoneErythropoietinPolycomb Repressive Complex 1Proto-Oncogene ProteinsRNA, Small InterferingStem Cell Factor

Identifiers

PMID26028528
PMCPMC4471833

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.