Evidence map›Paper›PMID 38277391›Full record

ArticlePloS one2024

Rat hair-follicle-associated pluripotent (HAP) stem cells can differentiate into atrial or ventricular cardiomyocytes in culture controlled by specific supplementation.

Nanako Takaoka, Michiko Yamane, Ayami Hasegawa, Koya Obara, Kyoumi Shirai, Ryoichi Aki, Hiroyasu Hatakeyama, Yuko Hamada, Nobuko Arakawa, Manabu Tanaka and 2 more

Abstract read
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Nanako TakaokaDepartment of Dermatology, Kitasato University Graduate School of Medical Sciences, Kitasato University School of Medicine, Minami Ward, Sagamihara, Japan.ORCID 0000-0001-5408-7226
Michiko YamaneDepartment of Dermatology, Kitasato University Graduate School of Medical Sciences, Kitasato University School of Medicine, Minami Ward, Sagamihara, Japan.
Ayami HasegawaDepartment of Dermatology, Kitasato University Graduate School of Medical Sciences, Kitasato University School of Medicine, Minami Ward, Sagamihara, Japan.
Koya ObaraDepartment of Dermatology, Kitasato University School of Medicine, Kitasato University School of Medicine, Minami Ward, Sagamihara, Japan.
Kyoumi ShiraiDepartment of Dermatology, Kitasato University School of Medicine, Kitasato University School of Medicine, Minami Ward, Sagamihara, Japan.
Ryoichi AkiDepartment of Dermatology, Kitasato University School of Medicine, Kitasato University School of Medicine, Minami Ward, Sagamihara, Japan.
Hiroyasu HatakeyamaDepartment of Physiology, Kitasato University School of Medicine, Kitasato University School of Medicine, Minami Ward, Sagamihara, Japan.
Yuko HamadaDepartment of Dermatology, Kitasato University School of Medicine, Kitasato University School of Medicine, Minami Ward, Sagamihara, Japan.
Nobuko ArakawaDepartment of Dermatology, Kitasato University School of Medicine, Kitasato University School of Medicine, Minami Ward, Sagamihara, Japan.
Manabu TanakaBio-Imaging Center, Kitasato University School of Medicine, Minami Ward, Sagamihara, Japan.
Robert M HoffmanAntiCancer, Inc., San Diego, CA, United States of America.
Yasuyuki AmohDepartment of Dermatology, Kitasato University School of Medicine, Kitasato University School of Medicine, Minami Ward, Sagamihara, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There has been only limited success to differentiate adult stem cells into cardiomyocyte subtypes. In the present study, we have successfully induced beating atrial and ventricular cardiomyocytes from rat hair-follicle-associated pluripotent (HAP) stem cells, which are adult stem cells located in the bulge area. HAP stem cells differentiated into atrial cardiomyocytes in culture with the combination of isoproterenol, activin A, bone morphogenetic protein 4 (BMP4), basic fibroblast growth factor (bFGF), and cyclosporine A (CSA). HAP stem cells differentiated into ventricular cardiomyocytes in culture with the combination of activin A, BMP4, bFGF, inhibitor of Wnt production-4 (IWP4), and vascular endothelial growth factor (VEGF). Differentiated atrial cardiomyocytes were specifically stained for anti-myosin light chain 2a (MLC2a) antibody. Ventricular cardiomyocytes were specially stained for anti-myosin light chain 2v (MLC2v) antibody. Quantitative Polymerase Chain Reaction (qPCR) showed significant expression of MLC2a in atrial cardiomyocytes and MLC2v in ventricular cardiomyocytes. Both differentiated atrial and ventricular cardiomyocytes showed characteristic waveforms in Ca2+ imaging. Differentiated atrial and ventricular cardiomyocytes formed long myocardial fibers and beat as a functional syncytium, having a structure similar to adult cardiomyocytes. The present results demonstrated that it is possible to induce cardiomyocyte subtypes, atrial and ventricular cardiomyocytes, from HAP stem cells.

Indexed as

Myocytes, CardiacPluripotent Stem CellsAnimalsCell DifferentiationDietary SupplementsHair FollicleRatsVascular Endothelial Growth Factor AVascular Endothelial Growth Factor A

Identifiers

PMID38277391
PMCPMC10817212

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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.