Evidence map›Paper›PMID 29352121›Full record

ArticleScientific reports2018

Efficient differentiation of human pluripotent stem cells into skeletal muscle cells by combining RNA-based MYOD1-expression and POU5F1-silencing.

Tomohiko Akiyama, Saeko Sato, Nana Chikazawa-Nohtomi, Atsumi Soma, Hiromi Kimura, Shunichi Wakabayashi, Shigeru B H Ko, Minoru S H Ko

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

23 citing papers in PubMed, 38 citations in OpenAlex.

  1. Review
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  5. Scalable control of stem cell fate by riboswitch-regulated RNA viral vector without genomic integration.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
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  6. ZSCAN4-binding motif-TGCACAC is conserved and enriched in CA/TG microsatellites in both mouse and human genomes.DNA research : an international journal for rapid publication of reports on genes and genomes · 2024
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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

8 authors at 1 institution in 1 country.

Tomohiko AkiyamaDepartment of Systems Medicine, Keio University School of Medicine, Tokyo, 160, Japan.
Saeko SatoDepartment of Systems Medicine, Keio University School of Medicine, Tokyo, 160, Japan.
Nana Chikazawa-NohtomiDepartment of Systems Medicine, Keio University School of Medicine, Tokyo, 160, Japan.
Atsumi SomaDepartment of Systems Medicine, Keio University School of Medicine, Tokyo, 160, Japan.
Hiromi KimuraDepartment of Systems Medicine, Keio University School of Medicine, Tokyo, 160, Japan.
Shunichi WakabayashiDepartment of Systems Medicine, Keio University School of Medicine, Tokyo, 160, Japan.
Shigeru B H KoDepartment of Systems Medicine, Keio University School of Medicine, Tokyo, 160, Japan.
Minoru S H KoDepartment of Systems Medicine, Keio University School of Medicine, Tokyo, 160, Japan. ko.minoru@keio.jp.ORCID http://orcid.org/0000-0002-3530-3015
Keio University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Direct generation of skeletal muscle cells from human pluripotent stem cells (hPSCs) would be beneficial for drug testing, drug discovery, and disease modelling in vitro. Here we show a rapid and robust method to induce myogenic differentiation of hPSCs by introducing mRNA encoding MYOD1 together with siRNA-mediated knockdown of POU5F1 (also known as OCT4 or OCT3/4). This integration-free approach generates functional skeletal myotubes with sarcomere-like structure and a fusion capacity in several days. The POU5F1 silencing facilitates MYOD1 recruitment to the target promoters, which results in the significant activation of myogenic genes in hPSCs. Furthermore, deep sequencing transcriptome analyses demonstrated that POU5F1-knockdown upregulates the genes associated with IGF- and FGF-signaling and extracellular matrix that may also support myogenic differentiation. This rapid and direct differentiation method may have potential applications in regenerative medicine and disease therapeutics for muscle disorders such as muscular dystrophy.

Indexed as

Cell DifferentiationCell LineEmbryonic Stem CellsGene Expression RegulationGene Knockdown TechniquesGene SilencingHumansModels, BiologicalMuscle DevelopmentMuscle Fibers, SkeletalMyoD ProteinOctamer Transcription Factor-3Pluripotent Stem CellsMyoD1 myogenic differentiation proteinMyoD ProteinOctamer Transcription Factor-3POU5F1 protein, human

Identifiers

PMID29352121
PMCPMC5775307
OpenAlexW2783645747

What OpenQuestion holds

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LicenceCC BY
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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.