Evidence map›Paper›PMID 34307796›Full record

ArticleRegenerative therapy2021

Adipose-derived mesenchymal stem cells preserve cardiac function via ANT-1 in dilated cardiomyopathy hamster model.

Daisuke Mori, Shigeru Miyagawa, Takashi Kido, Hiroki Hata, Takayoshi Ueno, Koichi Toda, Toru Kuratani, Miwa Oota, Kotoe Kawai, Hayato Kurata and 2 more

Open access · goldAbstract read
In one paragraph

Article in Regenerative therapy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Article
  5. Review
  6. The Role of Stem Cells in the Treatment of Cardiovascular Diseases.International journal of molecular sciences · 2024
    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

12 authors at 2 institutions in 1 country.

Daisuke MoriDepartment of Cardiovascular Surgery, Osaka University Graduate School of Medicine, Suita, Japan.
Shigeru MiyagawaDepartment of Cardiovascular Surgery, Osaka University Graduate School of Medicine, Suita, Japan.
Takashi KidoDepartment of Cardiovascular Surgery, Osaka University Graduate School of Medicine, Suita, Japan.
Hiroki HataDepartment of Cardiovascular Surgery, Osaka University Graduate School of Medicine, Suita, Japan.
Takayoshi UenoDepartment of Cardiovascular Surgery, Osaka University Graduate School of Medicine, Suita, Japan.
Koichi TodaDepartment of Cardiovascular Surgery, Osaka University Graduate School of Medicine, Suita, Japan.
Toru KurataniDepartment of Cardiovascular Surgery, Osaka University Graduate School of Medicine, Suita, Japan.
Miwa OotaInstitute of Advanced Stem Cell Therapy, Osaka University, Osaka, Japan.
Kotoe KawaiInstitute of Advanced Stem Cell Therapy, Osaka University, Osaka, Japan.
Hayato KurataInstitute of Advanced Stem Cell Therapy, Osaka University, Osaka, Japan.
Hiroyuki NishidaMedical Center for Translational Research, Osaka University Hospital, Osaka, Japan.
Yoshiki SawaDepartment of Cardiovascular Surgery, Osaka University Graduate School of Medicine, Suita, Japan.
The University of Osaka · JPOsaka University Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionIdiopathic dilated cardiomyopathy (DCM) is associated with abnormalities in cytoskeletal proteins, mitochondrial ATP transporter, microvasculature, and fibrosis. Mesenchymal stem cells (MSCs) can ameliorate distressed mitochondrial and structural proteins, as well as fibrosis, via the paracrine effect of cytokines. This study aimed to investigate whether the transplantation of adipose tissue-derived MSCs (ADSCs) reverses histological and functional abnormalities in the distressed myocardium of DCM-like hamsters by modulating the expression of adenine nucleotide translocase 1 (ANT-1).

methodsEighteen weeks after birth, ADSCs were implanted onto the cardiac surface of δ-sarcoglycan (SG)-deficient hamsters or sham surgery was performed.

resultsLeft ventricular ejection fraction and end-systolic diameter were maintained in ADSC-treated animals for four weeks, ATP concentration was considerably elevated in the cardiomyocytes of these animals, and ANT-1 expression was significantly upregulated as well. The expression of extracellular matrix and myocardial cytoskeletal proteins, such as collagen, SG, and α-dystroglycan, did not differ between groups. However, significant improvements in myosin and Smad4 expression, cardiomyocyte hypertrophy, and capillary density occurred in the ADSC-treated group.

conclusionsWe demonstrated that ADSCs might maintain cardiac function in the DCM hamster model by enhancing ATP concentration, as well as mitochondrial transporter and myosin expression, indicating their potential for DCM treatment.

Indexed as

ADSC, Adipose tissue-derived mesenchymal stem cellsANOVA, Analyses of varianceATPEF, Ejection fractionHGF, Human growth factorIdiopathic dilated cardiomyopathyLV, Left ventricleMesenchymal stem cellsMitochondrial transporterOD, Optical densitySEM, Standard error of the meanTGFR, Transforming growth factor receptorVEGF, Vascular endothelial growth factor

Identifiers

PMID34307796
PMCPMC8278151
OpenAlexW3182764265

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.