Evidence map›Paper›PMID 18824743›Full record

ArticleCirculation2008

Comparison of different adult stem cell types for treatment of myocardial ischemia.

Koen E A van der Bogt, Ahmad Y Sheikh, Sonja Schrepfer, Grant Hoyt, Feng Cao, Katherine J Ransohoff, Rutger-Jan Swijnenburg, Jeremy Pearl, Andrew Lee, Michael Fischbein and 3 more

Abstract readComparative Study
In one paragraph

Article in Circulation, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 115 papers.

0numbers the graph read from it
0cells of the map it votes in
115citing papers in PubMed
–field-weighted citation impact
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

115 citing papers in PubMed.

  1. Trial
  2. The hydrocup: a hollow electrospun scaffold forbioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Review
  5. International journal of stem cells · 2023
    Review
  6. Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. NoninvasiveWorld journal of stem cells · 2020
    Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

55 more citing papers are in PubMed but not listed here.

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

13 authors.

Koen E A van der BogtLaboratory of Cardiothoracic Transplantation, Stanford University School of Medicine, Stanford, CA 94305-5324, USA.
Ahmad Y Sheikh
Sonja Schrepfer
Grant Hoyt
Feng Cao
Katherine J Ransohoff
Rutger-Jan Swijnenburg
Jeremy Pearl
Andrew Lee
Michael Fischbein
Christopher H Contag
Robert C Robbins
Joseph C Wu

Funding

Nanostructuring and Molecular Imaging of Engineered Cardiovascular TissuesR33HL089027 · NHLBI · STANFORD UNIVERSITY · PI WU, JOSEPH C. · 2009 to 2011
$2.3M
Nanostructuring and Molecular Imaging of Engineered Cardiovascular TissuesR21HL089027 · NHLBI · STANFORD UNIVERSITY · PI WU, JOSEPH C. · 2007 to 2008
$777k
Molecular Imaging of Cardiac Cell TransplantationK08HL074883 · NHLBI · STANFORD UNIVERSITY · PI WU, JOSEPH C. · 2005 to 2008
$531k
NHLBI NIH HHS HL074883NHLBI NIH HHS HL089027NHLBI NIH HHS K08 HL074883NHLBI NIH HHS R21 HL089027NHLBI NIH HHS R33 HL089027
6 · The paper itself

Abstract

backgroundA comparative analysis of the efficacy of different cell candidates for the treatment of heart disease remains to be described. This study is designed to evaluate the therapeutic efficacy of 4 cell types in a murine model of myocardial infarction. METHODS AND

resultsBone marrow mononuclear cells (MN), mesenchymal stem cells (MSC), skeletal myoblasts (SkMb), and fibroblasts (Fibro) expressing firefly luciferase (Fluc) and green fluorescence protein (GFP) were characterized by flow cytometry, bioluminescence imaging (BLI), and luminometry. Female FVB mice (n=70) underwent LAD ligation and intramyocardially received one cell type (5x10(5)) or PBS. Cell survival was measured by BLI and by TaqMan PCR. Cardiac function was assessed by echocardiography and invasive hemodynamic measurements. Fluc expression correlated with cell number in all groups (r(2)>0.93). In vivo BLI revealed acute donor cell death of MSC, SkMb, and Fibro within 3 weeks after transplantation. By contrast, cardiac signals were still present after 6 weeks in the MN group, as confirmed by TaqMan PCR (P<0.01). Echocardiography showed significant preservation of fractional shortening in the MN group compared to controls (P<0.05). Measurements of left ventricular end-systolic/diastolic volumes revealed that the least amount of ventricular dilatation occurred in the MN group (P<0.05). Histology confirmed the presence of MN, although there was no evidence of transdifferentiation by donor MN into cardiomyocytes.

conclusionsThis is the first study to show that compared to MSC, SkMB, and Fibro, MN exhibit a more favorable survival pattern, which translates into a more robust preservation of cardiac function.

Indexed as

Stem Cell TransplantationAnimalsBone Marrow CellsBone Marrow TransplantationCell SurvivalEchocardiographyFemaleFibroblastsGreen Fluorescent ProteinsLuciferases, FireflyMaleMesenchymal Stem Cell TransplantationMiceMice, Inbred StrainsMice, TransgenicMyoblasts, SkeletalGreen Fluorescent ProteinsLuciferases, Firefly

Identifiers

PMID18824743
PMCPMC3657517

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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.