Evidence map›Paper›PMID 22491213›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2012

SCL/TAL1 regulates hematopoietic specification from human embryonic stem cells.

Pedro J Real, Gertrudis Ligero, Veronica Ayllon, Veronica Ramos-Mejia, Clara Bueno, Ivan Gutierrez-Aranda, Oscar Navarro-Montero, Majlinda Lako, Pablo Menendez

Open access · bronzeAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

40 citing papers in PubMed, 66 citations in OpenAlex.

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  18. Intragenic CpG islands play important roles in bivalent chromatin assembly of developmental genes.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  19. Article
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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

9 authors at 3 institutions in 2 countries.

Pedro J RealPfizer-Universidad de Granada-Junta de Andalucia Centre for Genomics and Oncological Research (GENyO), Granada, Spain. pedro.real@genyo.es
Gertrudis Ligero
Veronica Ayllon
Veronica Ramos-Mejia
Clara Bueno
Ivan Gutierrez-Aranda
Oscar Navarro-Montero
Majlinda Lako
Pablo Menendez
Universidad de Granada · ESNewcastle University · GBPfizer-University of Granada-Junta de Andalucía Centre for Genomics and Oncological Research · ES

Funding

Biotechnology and Biological Sciences Research Council BB/E012841/1Medical Research Council G0301182
6 · The paper itself

Abstract

Determining the molecular regulators/pathways responsible for the specification of human embryonic stem cells (hESCs) into hematopoietic precursors has far-reaching implications for potential cell therapies and disease modeling. Mouse models lacking SCL/TAL1 (stem cell leukemia/T-cell acute lymphocytic leukemia 1) do not survive beyond early embryogenesis because of complete absence of hematopoiesis, indicating that SCL is a master early hematopoietic regulator. SCL is commonly found rearranged in human leukemias. However, there is barely information on the role of SCL on human embryonic hematopoietic development. Differentiation and sorting assays show that endogenous SCL expression parallels hematopoietic specification of hESCs and that SCL is specifically expressed in hematoendothelial progenitors (CD45(-)CD31(+)CD34(+)) and, to a lesser extent, on CD45(+) hematopoietic cells. Enforced expression of SCL in hESCs accelerates the emergence of hematoendothelial progenitors and robustly promotes subsequent differentiation into primitive (CD34(+)CD45(+)) and total (CD45(+)) blood cells with higher clonogenic potential. Short-hairpin RNA-based silencing of endogenous SCL abrogates hematopoietic specification of hESCs, confirming the early hematopoiesis-promoting effect of SCL. Unfortunately, SCL expression on its own is not sufficient to confer in vivo engraftment to hESC-derived hematopoietic cells, suggesting that additional yet undefined master regulators are required to orchestrate the stepwise hematopoietic developmental process leading to the generation of definitive in vivo functional hematopoiesis from hESCs.

Indexed as

AnimalsAntigens, CD34Basic Helix-Loop-Helix ProteinsCell DifferentiationCell LineEmbryonic Stem CellsHematopoiesisHumansLeukocyte Common AntigensMicePlatelet Endothelial Cell Adhesion Molecule-1Proto-Oncogene ProteinsRNA InterferenceRNA, Small InterferingT-Cell Acute Lymphocytic Leukemia Protein 1Antigens, CD34Basic Helix-Loop-Helix ProteinsLeukocyte Common AntigensPlatelet Endothelial Cell Adhesion Molecule-1Proto-Oncogene ProteinsRNA, Small InterferingTAL1 protein, humanT-Cell Acute Lymphocytic Leukemia Protein 1

Identifiers

PMID22491213
PMCPMC3392972
OpenAlexW2021957728

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.