Evidence map›Paper›PMID 22438249›Full record

ArticleBlood2012

Dynamic HoxB4-regulatory network during embryonic stem cell differentiation to hematopoietic cells.

Rong Fan, Sabrina Bonde, Peng Gao, Brendan Sotomayor, Changya Chen, Tyler Mouw, Nicholas Zavazava, Kai Tan

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

33 citing papers in PubMed, 64 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. eLife · 2020
    Article
  9. Article
  10. Review
  11. Article
  12. A Case of Identity:Cancers · 2019
    Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. NPInter v3.0: an upgraded database of noncoding RNA-associated interactions.Database : the journal of biological databases and curation · 2016
    Article
  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 1 country.

Rong FanDepartment of Internal Medicine, University of Iowa, Iowa City, IA 52242, USA.
Sabrina Bonde
Peng Gao
Brendan Sotomayor
Changya Chen
Tyler Mouw
Nicholas Zavazava
Kai Tan
University of Iowa · USVeterans Health Administration · US

Funding

EMBRYONIC STEM CELLS INDUCE SPECIFIC GRAFT TOLERANCER01HL073015 · NHLBI · UNIVERSITY OF IOWA · PI ZAVAZAVA, NICHOLAS · 2004 to 2012
$2.5M
EPIGENETIC REGULATION OF STEM CELL FATE CHOICER01HG006130 · NHGRI · UNIVERSITY OF IOWA · PI TAN, KAI · 2012 to 2016
$1.7M
Viral-induced demyelination and neural stem cell-mediated remyelinationR01NS074987 · NINDS · UNIVERSITY OF UTAH · PI LANE, THOMAS E · 2011 to 2015
$1.6M
STEM CELL-DERIVED INSUIN PRODUCING CELLS CORRECT HYPERGLYCEMIA IN DIABETIC MICEI01BX001125 · VA · IOWA CITY VA MEDICAL CENTER · PI ZAVAZAVA, NICHOLAS · 2012 to 2015
–
BLRD VA I01 BX001125NHGRI NIH HHS R01 HG006130NHLBI NIH HHS R01 HL073015NHLBI NIH HHS R01HL073015NINDS NIH HHS R01 NS074987NINDS NIH HHS R01NS074987
6 · The paper itself

Abstract

Efficient in vitro generation of hematopoietic stem cells (HSCs) from embryonic stem cells (ESCs) holds great promise for cell-based therapies to treat hematologic diseases. To date, HoxB4 remains the most effective transcription factor (TF) the overexpression of which in ESCs confers long-term repopulating ability to ESC-derived HSCs. Despite its importance, the components and dynamics of the HoxB4 transcriptional regulatory network is poorly understood, hindering efforts to develop more efficient protocols for in vitro derivation of HSCs. In the present study, we performed global gene-expression profiling and ChIP coupled with deep sequencing at 4 stages of the HoxB4-mediated ESC differentiation toward HSCs. Joint analyses of ChIP/deep sequencing and gene-expression profiling unveiled several global features of the HoxB4 regulatory network. First, it is highly dynamic and gradually expands during the differentiation process. Second, HoxB4 functions as a master regulator of hematopoiesis by regulating multiple hematopoietic TFs and chromatin-modification enzymes. Third, HoxB4 acts in different combinations with 4 other hematopoietic TFs (Fli1, Meis1, Runx1, and Scl) to regulate distinct sets of pathways. Finally, the results of our study suggest that down-regulation of mitochondria and lysosomal genes by HoxB4 plays a role in the impaired lymphoid lineage development from ESC-derived HSCs.

Indexed as

AnimalsBlood CellsCell DifferentiationCell LineageCells, CulturedEmbryonic Stem CellsGene Expression ProfilingGene Expression Regulation, DevelopmentalGene Regulatory NetworksHematopoiesisHematopoietic Stem CellsHomeodomain ProteinsHumansLymphocytesMiceMicroarray AnalysisHomeodomain ProteinsHOXB4 protein, humanTranscription Factors

Identifiers

PMID22438249
PMCPMC3362371
OpenAlexW1996261354

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.