Evidence map›Paper›PMID 16093308›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2005

HOXB4 enforces equivalent fates of ES-cell-derived and adult hematopoietic cells.

Sandra Pilat, Sebastian Carotta, Bernhard Schiedlmeier, Kenji Kamino, Andreas Mairhofer, Elke Will, Ute Modlich, Peter Steinlein, Wolfram Ostertag, Christopher Baum and 2 more

Open access · greenAbstract readComparative Study
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
3.5field-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

42 citing papers in PubMed, 83 citations in OpenAlex.

  1. Review
  2. Article
  3. HOXB4 IncreasesTransfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie · 2017
    Article
  4. Article
  5. Article
  6. Generation of engraftable hematopoietic stem cells from induced pluripotent stem cells by way of teratoma formation.Molecular therapy : the journal of the American Society of Gene Therapy · 2013
    Article
  7. Article
  8. Article
  9. Erythropoiesis: development and differentiation.Cold Spring Harbor perspectives in medicine · 2013
    Review
  10. Review
  11. Article
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  13. Article
  14. Embryonic stem cell-derived T cells induce lethal graft-versus-host disease and reject allogenic skin grafts upon thymic selection.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2012
    Article
  15. Article
  16. Review
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  18. Review
  19. Specific erythroid-lineage defect in mice conditionally deficient for Mediator subunit Med1.Proceedings of the National Academy of Sciences of the United States of America · 2010
    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

12 authors at 4 institutions in 3 countries.

Sandra PilatResearch Institute of Molecular Pathology, Vienna Biocenter, Dr. Bohr-Gasse 7, 1030 Vienna, Austria.
Sebastian Carotta
Bernhard Schiedlmeier
Kenji Kamino
Andreas Mairhofer
Elke Will
Ute Modlich
Peter Steinlein
Wolfram Ostertag
Christopher Baum
Hartmut Beug
Hannes Klump
Vienna Biocenter · ATCincinnati Children's Hospital Medical Center · USResearch Institute of Molecular Pathology · ATMedizinische Hochschule Hannover · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetic manipulation of hematopoietic stem and progenitor cells is an important tool for experimental and clinical applied hematology. However, techniques that allow for gene targeting, subsequent in vitro selection, and expansion of genetically defined clones are available only for ES cells. Such molecularly defined and, hence, "safe" clones would be highly desirable for somatic gene therapy. Here, we demonstrate that in vitro differentiated ES cells completely recapitulate the growth and differentiation properties of adult bone marrow cells, in vitro and in vivo, when ectopically expressing HOXB4. Myeloid development was enforced and (T) lymphoid development suppressed over a wide range of expression levels, whereas only high expression levels of the transcription factor were detrimental for erythroid development. This indicates a close association between the amounts of ectopic HOXB4 present within a progenitor cell and and the decision to self renew or differentiate. Because HOXB4 mediates similar fates of ES-derived and bone marrow hematopoietic stem cells, the primitive embryonic cells can be considered a promising alternative for investigating hematopoietic reconstitution, in vivo, based on well defined clones. Provided that HOXB4 levels are kept within a certain therapeutic window, ES cells also carry the potential of efficient and safe somatic gene therapy.

Indexed as

Gene ExpressionAnimalsBone Marrow CellsCell DifferentiationFlow CytometryGenetic VectorsHematopoietic Stem CellsHomeodomain ProteinsMiceRetroviridaeTranscription FactorsHomeodomain ProteinsHoxb4 protein, mouseTranscription Factors

Identifiers

PMID16093308
PMCPMC1189347
OpenAlexW2105400510

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.