Evidence map›Paper›PMID 27304057›Full record

ArticleOncotarget2016

Human pluripotent stem cell (PSC)-derived mesenchymal stem cells (MSCs) show potent neurogenic capacity which is enhanced with cytoskeletal rearrangement.

Kai-Yen Peng, Yu-Wei Lee, Pei-Ju Hsu, Hsiu-Huan Wang, Yun Wang, Jun-Yang Liou, Shan-Hui Hsu, Kenneth K Wu, B Linju Yen

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.9field-weighted citation impact, top 24% 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

16 citing papers in PubMed, 21 citations in OpenAlex.

  1. Stem Cells Run Like Clockwork for Stroke Therapeutics.Stem cell reviews and reports · 2025
    Article
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  6. Review
  7. Article
  8. Review
  9. PSC-MSC-Derived Exosomes Protect against Kidney FibrosisInternational journal of stem cells · 2021
    Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Human iPSC banking: barriers and opportunities.Journal of biomedical science · 2019
    Review
  16. 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

9 authors at 4 institutions in 1 country.

Kai-Yen PengDepartment of Life Science, National Central University, Jhongli, Taiwan.
Yu-Wei LeeRegenerative Medicine Research Group, Institute of Cellular and System Medicine, National Health Research Institutes (NHRI), Zhunan, Taiwan.
Pei-Ju HsuRegenerative Medicine Research Group, Institute of Cellular and System Medicine, National Health Research Institutes (NHRI), Zhunan, Taiwan.
Hsiu-Huan WangRegenerative Medicine Research Group, Institute of Cellular and System Medicine, National Health Research Institutes (NHRI), Zhunan, Taiwan.
Yun WangCenter for Neuropsychiatric Research, NHRI, Zhunan, Taiwan.
Jun-Yang LiouRegenerative Medicine Research Group, Institute of Cellular and System Medicine, National Health Research Institutes (NHRI), Zhunan, Taiwan.
Shan-Hui HsuInstitute of Polymer Science and Engineering, National Taiwan University, Taipei, Taiwan.
Kenneth K WuGraduate Institute of Basic Medical Sciences, China Medical University, Taichung, Taiwan.
B Linju YenRegenerative Medicine Research Group, Institute of Cellular and System Medicine, National Health Research Institutes (NHRI), Zhunan, Taiwan.
National Health Research Institutes · TWChina Medical University · TWNational Central University · TWNational Taiwan University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mesenchymal stem cells (MSCs) are paraxial mesodermal progenitors with potent immunomodulatory properties. Reports also indicate that MSCs can undergo neural-like differentiation, offering hope for use in neurodegenerative diseases. However, ex vivo expansion of these rare somatic stem cells for clinical use leads to cellular senescence. A newer source of MSCs derived from human pluripotent stem cells (PSC) can offer the 'best-of-both-worlds' scenario, abrogating the concern of teratoma formation while preserving PSC proliferative capacity. PSC-derived MSCs (PSC-MSCs) also represent MSCs at the earliest developmental stage, and we found that these MSCs harbor stronger neuro-differentiation capacity than post-natal MSCs. PSC-MSCs express higher levels of neural stem cell (NSC)-related genes and transcription factors than adult bone marrow MSCs at baseline, and rapidly differentiate into neural-like cells when cultured in either standard neurogenic differentiation medium (NDM) or when the cytoskeletal modulator RhoA kinase (ROCK) is inhibited. Interestingly, when NDM is combined with ROCK inhibition, PSC-MSCs undergo further commitment, acquiring characteristics of post-mitotic neurons including nuclear condensation, extensive dendritic growth, and neuron-restricted marker expression including NeuN, β-III-tubulin and Doublecortin. Our data demonstrates that PSC-MSCs have potent capacity to undergo neural differentiation and also implicate the important role of the cytoskeleton in neural lineage commitment.

Indexed as

CytoskeletonCell DifferentiationCell LineageHumansMesenchymal Stem CellsNeural Stem CellsPluripotent Stem Cellsrho-Associated Kinasesrho-Associated Kinaseshuman embryonic stem cells (ESCs)human pluripotent stem cells (PSC)induced pluripotent stem cells (iPS)mesenchymal stem cells (MSCs)Rho A kinase (ROCK)

Identifiers

PMID27304057
PMCPMC5190070
OpenAlexW2416332150

What OpenQuestion holds

Textmetadata
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.