Evidence map›Paper›PMID 24558402›Full record

ArticlePloS one2014

Angiogenesis, cardiomyocyte proliferation and anti-fibrotic effects underlie structural preservation post-infarction by intramyocardially-injected cardiospheres.

Eleni Tseliou, Geoffrey de Couto, John Terrovitis, Baiming Sun, Liu Weixin, Linda Marbán, Eduardo Marbán

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
9.7field-weighted citation impact, top 1% 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

35 citing papers in PubMed, 64 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Cell Therapy in the Treatment of Coronary Heart Disease.International journal of molecular sciences · 2023
    Review
  6. Article
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  15. Article
  16. Review
  17. Cardiac Progenitor Cells: The Matrix Has You.Stem cells translational medicine · 2018
    Article
  18. Article
  19. Article
  20. Is Cardioprotection Dead?Circulation · 2017
    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

7 authors at 2 institutions in 2 countries.

Eleni TseliouHeart Institute, Cedars-Sinai Medical Center, Los Angeles, California, United States of America.
Geoffrey de CoutoHeart Institute, Cedars-Sinai Medical Center, Los Angeles, California, United States of America.
John TerrovitisThird Department of Cardiology, University of Athens, Athens, Greece.
Baiming SunHeart Institute, Cedars-Sinai Medical Center, Los Angeles, California, United States of America.
Liu WeixinHeart Institute, Cedars-Sinai Medical Center, Los Angeles, California, United States of America.
Linda MarbánHeart Institute, Cedars-Sinai Medical Center, Los Angeles, California, United States of America.
Eduardo MarbánHeart Institute, Cedars-Sinai Medical Center, Los Angeles, California, United States of America.
Cedars-Sinai Medical Center · USNational and Kapodistrian University of Athens · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveWe sought to understand the cellular and tissue-level changes underlying the attenuation of adverse remodeling by cardiosphere transplantation in acute myocardial infarction (MI).

backgroundCardiospheres (CSps) are heart-derived multicellular clusters rich in stemness and capable of multilineage differentiation. Post-MI CSp transplantation improves left ventricular (LV) function and attenuates remodeling in both small and large animal studies. However, the mechanisms of benefit have not yet been fully elucidated.

methodsFour groups were studied: 1) "Sham" (Wistar Kyoto rats with thoracotomy and ligature without infarction); 2) "MI" (proximal LAD ligation with peri-infarct injection of vehicle); 3) "MI+CSp" (MI with cardiospheres injected in the peri-infarct area); 4) "Small MI" (mid-LAD ligation only).

resultsIn vivo 1 week after CSp transplantation, LV functional improvement was associated with an increase in cardiomyocyte proliferation. By 3 weeks, microvessel formation was enhanced, while cardiomyocyte hypertrophy and regional fibrosis were attenuated. Collagen deposition was reduced, collagen degradation was enhanced, and MMPs were upregulated. The beneficial effects of CSp transplantation were not observed in the Small MI group, indicating that the effects are not solely due to CSp-induced cardioprotection. In vitro, CSp-conditioned media reduced collagen production in coculture with fibroblasts and triggered neoangiogenesis in an ex vivo aortic ring assay.

conclusionCardiospheres enhance cardiomyocyte proliferation and angiogenesis, and attenuate hypertrophy and fibrosis, in the ischemic myocardium. These synergistic effects underlie the attenuation of adverse remodeling by cardiospheres.

Indexed as

Neovascularization, PathologicAnimalsCell LineageCell ProliferationCoculture TechniquesCollagenCulture Media, ConditionedEchocardiographyFemaleFibrosisHeartHypertrophyInflammationMicrocirculationMyocardial InfarctionMyocardiumCollagenCulture Media, Conditioned

Identifiers

PMID24558402
PMCPMC3928273
OpenAlexW2016165259

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Registered trials

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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.