Evidence map›Paper›PMID 28026072›Full record

ArticleStem cells (Dayton, Ohio)2017

Activation of KLF1 Enhances the Differentiation and Maturation of Red Blood Cells from Human Pluripotent Stem Cells.

Cheng-Tao Yang, Rui Ma, Richard A Axton, Melany Jackson, A Helen Taylor, Antonella Fidanza, Lamin Marenah, Jan Frayne, Joanne C Mountford, Lesley M Forrester

Abstract read
In one paragraph

Article in Stem cells (Dayton, Ohio), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing 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

37 citing papers in PubMed.

  1. Article
  2. Orai1 acts as a novel CaExperimental & molecular medicine · 2026
    Article
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  20. 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
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.

Cheng-Tao YangCentre for Regenerative Medicine, University of Edinburgh, Edinburgh, United Kingdom.
Rui MaCentre for Regenerative Medicine, University of Edinburgh, Edinburgh, United Kingdom.
Richard A AxtonCentre for Regenerative Medicine, University of Edinburgh, Edinburgh, United Kingdom.
Melany JacksonCentre for Regenerative Medicine, University of Edinburgh, Edinburgh, United Kingdom.
A Helen TaylorCentre for Regenerative Medicine, University of Edinburgh, Edinburgh, United Kingdom.
Antonella FidanzaCentre for Regenerative Medicine, University of Edinburgh, Edinburgh, United Kingdom.
Lamin MarenahInstitute of Cardiovascular & Medical Sciences, University of Glasgow, Glasgow, United Kingdom.
Jan FrayneDepartment of Biochemistry, University of Bristol, United Kingdom.
Joanne C MountfordInstitute of Cardiovascular & Medical Sciences, University of Glasgow, Glasgow, United Kingdom.
Lesley M ForresterCentre for Regenerative Medicine, University of Edinburgh, Edinburgh, United Kingdom.

Funding

Medical Research Council MR/K017047/1Medical Research Council MR/L012766/1Wellcome Trust
6 · The paper itself

Abstract

Blood transfusion is widely used in the clinic but the source of red blood cells (RBCs) is dependent on donors, procedures are susceptible to transfusion-transmitted infections and complications can arise from immunological incompatibility. Clinically-compatible and scalable protocols that allow the production of RBCs from human embryonic stem cells (hESCs) and induced pluripotent stem cells (iPSCs) have been described but progress to translation has been hampered by poor maturation and fragility of the resultant cells. Genetic programming using transcription factors has been used to drive lineage determination and differentiation so we used this approach to assess whether exogenous expression of the Erythroid Krüppel-like factor 1 (EKLF/KLF1) could augment the differentiation and stability of iPSC-derived RBCs. To activate KLF1 at defined time points during later stages of the differentiation process and to avoid transgene silencing that is commonly observed in differentiating pluripotent stem cells, we targeted a tamoxifen-inducible KLF1-ER

Indexed as

Cell DifferentiationCell NucleusCell ProliferationErythrocytesErythropoiesisGene Expression RegulationGlobinsHematopoietic Stem CellsHumansInduced Pluripotent Stem CellsK562 CellsKruppel-Like Transcription FactorsProtein TransportRecombinant Fusion Proteinserythroid Kruppel-like factorGlobinsKruppel-Like Transcription FactorsRecombinant Fusion ProteinsErythroid differentiationGene delivery systems in vivo or in vitroInduced pluripotent stem cellsTranscription factors

Identifiers

PMID28026072
PMCPMC5396323

What OpenQuestion holds

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LicenceCC BY
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.