Evidence map›Paper›PMID 27251161›Full record

ArticleIn vitro cellular & developmental biology. Animal2016

Induction of specific neuron types by overexpression of single transcription factors.

Yusuke Teratani-Ota, Kohei Yamamizu, Yulan Piao, Lioudmila Sharova, Misa Amano, Hong Yu, David Schlessinger, Minoru S H Ko, Alexei A Sharov

Abstract read
In one paragraph

Article in In vitro cellular & developmental biology. Animal, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.5field-weighted citation impact, top 29% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

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  13. NovelCold Spring Harbor molecular case studies · 2017
    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

9 authors at 3 institutions in 2 countries.

Yusuke Teratani-OtaLaboratory of Genetics, National Institute on Aging, National Institutes of Health, Baltimore, MD, 21224, USA.
Kohei YamamizuLaboratory of Genetics, National Institute on Aging, National Institutes of Health, Baltimore, MD, 21224, USA.
Yulan PiaoLaboratory of Genetics, National Institute on Aging, National Institutes of Health, Baltimore, MD, 21224, USA.
Lioudmila SharovaLaboratory of Genetics, National Institute on Aging, National Institutes of Health, Baltimore, MD, 21224, USA.
Misa AmanoLaboratory of Genetics, National Institute on Aging, National Institutes of Health, Baltimore, MD, 21224, USA.
Hong YuLaboratory of Genetics, National Institute on Aging, National Institutes of Health, Baltimore, MD, 21224, USA.
David SchlessingerLaboratory of Genetics, National Institute on Aging, National Institutes of Health, Baltimore, MD, 21224, USA.
Minoru S H KoDepartment of Systems Medicine, Sakaguchi Laboratory, Keio University School of Medicine, Tokyo, 160-8582, Japan.
Alexei A SharovLaboratory of Genetics, National Institute on Aging, National Institutes of Health, Baltimore, MD, 21224, USA. sharoval@mail.nih.gov.
National Institutes of Health · USNational Institute on Aging · USKeio University · JP

Funding

Placenta specific and ribosomal RNA genes: structure and functionZIAAG000646 · NIA · NATIONAL INSTITUTE ON AGING · PI NAGARAJA, RAMAIAH · 2009 to 2025
$12.9M
Systematic analysis of gene regulatory networksZIAAG000656 · NIA · NATIONAL INSTITUTE ON AGING · PI SCHLESSINGER, DAVID · 2009 to 2016
$3.9M
Systematic analysis of gene regulatory networksZ01AG000656 · NIA · NATIONAL INSTITUTE ON AGING · PI KO, MINORU S · 1999 to 2008
$1.6M
Intramural NIH HHS Z01 AG000656Intramural NIH HHS ZIA AG000656
6 · The paper itself

Abstract

Specific neuronal types derived from embryonic stem cells (ESCs) can facilitate mechanistic studies and potentially aid in regenerative medicine. Existing induction methods, however, mostly rely on the effects of the combined action of multiple added growth factors, which generally tend to result in mixed populations of neurons. Here, we report that overexpression of specific transcription factors (TFs) in ESCs can rather guide the differentiation of ESCs towards specific neuron lineages. Analysis of data on gene expression changes 2 d after induction of each of 185 TFs implicated candidate TFs for further ESC differentiation studies. Induction of 23 TFs (out of 49 TFs tested) for 6 d facilitated neural differentiation of ESCs as inferred from increased proportion of cells with neural progenitor marker PSA-NCAM. We identified early activation of the Notch signaling pathway as a common feature of most potent inducers of neural differentiation. The majority of neuron-like cells generated by induction of Ascl1, Smad7, Nr2f1, Dlx2, Dlx4, Nr2f2, Barhl2, and Lhx1 were GABA-positive and expressed other markers of GABAergic neurons. In the same way, we identified Lmx1a and Nr4a2 as inducers for neurons bearing dopaminergic markers and Isl1, Fezf2, and St18 for cholinergic motor neurons. A time-course experiment with induction of Ascl1 showed early upregulation of most neural-specific messenger RNA (mRNA) and microRNAs (miRNAs). Sets of Ascl1-induced mRNAs and miRNAs were enriched in Ascl1 targets. In further studies, enrichment of cells obtained with the induction of Ascl1, Smad7, and Nr2f1 using microbeads resulted in essentially pure population of neuron-like cells with expression profiles similar to neural tissues and expressed markers of GABAergic neurons. In summary, this study indicates that induction of transcription factors is a promising approach to generate cultures that show the transcription profiles characteristic of specific neural cell types.

Indexed as

NeurogenesisAnimalsBasic Helix-Loop-Helix ProteinsCellular ReprogrammingCOUP Transcription Factor IGene Expression ProfilingMiceMouse Embryonic Stem CellsNeuronsSmad7 ProteinTranscription FactorsTranscriptomeUp-RegulationAscl1 protein, mouseBasic Helix-Loop-Helix ProteinsCOUP Transcription Factor INr2f1 protein, mouseSmad7 ProteinTranscription FactorsAscl1Cholinergic neuronsDopaminergic neuronsESCsGABAergic neuronsGene expression profilingmiRNA

Identifiers

PMID27251161
PMCPMC5518781
OpenAlexW2410545495

What OpenQuestion holds

Textmetadata
LicenceTDM
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.