Evidence map›Paper›PMID 27405982›Full record

ArticleStem cell research & therapy2016

The role of nuclear factor of activated T cells during phorbol myristate acetate-induced cardiac differentiation of mesenchymal stem cells.

Hyang-Hee Seo, Chang Youn Lee, Jiyun Lee, Soyeon Lim, Eunhyun Choi, Jong-Chul Park, Seahyoung Lee, Ki-Chul Hwang

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 31% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

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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 2 institutions in 1 country.

Hyang-Hee SeoBrain Korea 21 PLUS Project for Medical Science, Yonsei University, Seoul, South Korea.
Chang Youn LeeDepartment of Integrated Omics for Biomedical Sciences, Yonsei University, Seoul, South Korea.
Jiyun LeeBrain Korea 21 PLUS Project for Medical Science, Yonsei University, Seoul, South Korea.
Soyeon LimInstitute for Bio-medical Convergence, Catholic Kwandong University, Incheon, South Korea.
Eunhyun ChoiInstitute for Bio-medical Convergence, Catholic Kwandong University, Incheon, South Korea.
Jong-Chul ParkCellbiocontrol Laboratory, Department of Medical Engineering, Yonsei University College of Medicine, Seoul, South Korea.
Seahyoung LeeInstitute for Bio-medical Convergence, Catholic Kwandong University, Incheon, South Korea. sam1017@ish.ac.kr.
Ki-Chul HwangInstitute for Bio-medical Convergence, Catholic Kwandong University, Incheon, South Korea. kchwang@cku.ac.kr.
Catholic Kwandong University · KRYonsei University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWe previously reported that phorbol 12-myristate 13-acetate (PMA) treatment can induce the cardiac differentiation of mesenchymal stem cells (MSCs). In the present study, we investigated how PMA induces cardiac differentiation of MSCs, focusing on its effect on the transcription factors responsible for increased cardiac marker gene expression.

methodsHuman MSCs (hMSCs) were treated with 1 μM PMA for 9 days. The expression of MSC markers and cardiac markers in the PMA-treated hMSC, as well as the nuclear translocation of transcription factors, nuclear factor of activated T cells (NFAT), and myogenic differentiation 1 (MyoD), was examined. Transcriptional activity of NFAT was examined by utilizing a green fluorescent protein (GFP) vector containing NFAT motif of human interleukin-2 promoter. The effect of PMA on the expression of key cell cycle regulators was examined.

resultsPMA induces the transcriptional activity of NFAT and MyoD, which have been associated with increased expression of cardiac troponin T (cTnT) and myosin heavy chain (MHC), respectively. Our data suggested that protein kinase C (PKC) mediates the effect of PMA on NFAT activation. Furthermore, PMA treatment increased cell-cycle regulator p27(kip1) expression, suggesting that PMA triggers the cardiac differentiation program in MSCs by regulating key transcription factors and cell cycle regulators.

conclusionsThe results of this study demonstrate the importance of NFAT activation during PMA-induced MSC differentiation and help us to better understand the underlying mechanisms of small molecule-mediated MSC differentiation so that we can develop a strategy for synthesizing novel and improved differentiation-inducing small molecules.

Indexed as

Cell CycleCell DifferentiationCyclin-Dependent Kinase Inhibitor p27Gene Expression RegulationGenes, ReporterGreen Fluorescent ProteinsHumansLymphocyte ActivationMesenchymal Stem CellsMyocytes, CardiacMyoD ProteinMyosin Heavy ChainsNFATC Transcription FactorsPrimary Cell CultureProtein Kinase CSignal TransductionCDKN1B protein, humanCyclin-Dependent Kinase Inhibitor p27Green Fluorescent ProteinsMyoD1 myogenic differentiation proteinMyoD ProteinMyosin Heavy ChainsNFATC Transcription FactorsProtein Kinase CTetradecanoylphorbol AcetateTroponin TCardiac differentiationMSCNFATPhorbol myristate acetateSmall molecule

Identifiers

PMID27405982
PMCPMC4942985
OpenAlexW2464769698

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.