Evidence map›Paper›PMID 22135400›Full record

ArticleCirculation. Cardiovascular imaging2012

Molecular imaging of mesenchymal stem cell: mechanistic insight into cardiac repair after experimental myocardial infarction.

Jingxiong Wang, Amer Najjar, Sui Zhang, Brian Rabinovich, James T Willerson, Juri G Gelovani, Edward T H Yeh

Abstract read
In one paragraph

Article in Circulation. Cardiovascular imaging, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Molecular Imaging in Drug Discovery and Development.Circulation. Cardiovascular imaging · 2018
    Review
  5. Article
  6. Article
  7. In vivo cell tracking with bioluminescence imaging.Nuclear medicine and molecular imaging · 2015
    Review
  8. Molecular imaging of stem cells for the treatment of acute myocardial infarction.International journal of clinical and experimental medicine · 2015
    Article
  9. Article
  10. Article
  11. Review
  12. Article
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.

Jingxiong WangTexas Heart Institute at St. Luke's Episcopal Hospital, Houston, TX, USA.
Amer Najjar
Sui Zhang
Brian Rabinovich
James T Willerson
Juri G Gelovani
Edward T H Yeh

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Experimental Cancer Imaging Research Program (ECIRP)U24CA126577 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI GELOVANI, JURI GEORGE, HAZLE, JOHN D. · 2007 to 2011
$2.2M
Molecular Imaging of Stem Cell Transplantation in the HeartR01HL086983 · NHLBI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI GELOVANI, JURI GEORGE · 2007 to 2010
$1.5M
CIHRNCI NIH HHS P30 CA016672NCI NIH HHS P30-CA016672NCI NIH HHS U24 CA126577NCI NIH HHS U24-CA126577NHLBI NIH HHS R01 HL086983
6 · The paper itself

Abstract

backgroundMesenchymal stem cells (MSCs) can differentiate into endothelial cells in vivo. However, it is unknown if the differentiated MSCs persist in vivo and if this potential persistence contributes to functional improvement after experimental myocardial infarction. METHODS AND

resultsWe generated a lentivector encoding 2 distinct reporter genes, one driven by a constitutive murine stem cell virus promoter and the other driven by an endothelial-specific Tie-2 promoter. The endothelial specificity of the lentivector was validated by its expression in endothelial cells but not in human MSCs (hMSCs). The lentivirus-transduced hMSCs were injected into peri-infarct areas of the hearts of severe combined immune-deficient mice. Persistence of injected cells was tracked by bioluminescence imaging (BLI) and verified by immunohistochemical staining. The BLI signal from the endothelial-specific reporter revealed that hMSCs differentiated into endothelial cells 48 hours after injection. However, both the constitutive and endothelial-specific BLI signals disappeared by day 50. Nonetheless, the improvement in left ventricle ejection fraction with hMSC therapy persisted for up to 6 months. Immunohistochemical staining showed that hMSC-derived endothelial cells integrated into endogenous CD31(+) vessels. Furthermore, hMSC-transplanted hearts had more CD31(+) vessels and a lesser degree of cardiac fibrosis compared with the controls at 6 months.

conclusionshMSCs differentiated into endothelial cells and integrated into blood vessels after experimental myocardial infarction. The differentiated hMSCs only lasted for up to 50 days in vivo, but improvement in cardiac function persisted for up to 6 months. Increased angiogenesis and decreased fibrosis were associated with cardiac functional improvement after hMSC transplantation.

Indexed as

Mesenchymal Stem Cell TransplantationVentricular Function, LeftAnimalsCell DifferentiationCells, CulturedDisease Models, AnimalEndothelial CellsFemaleFibrosisGenes, ReporterHumansLuminescent MeasurementsMagnetic Resonance ImagingMesenchymal Stem CellsMiceMice, Inbred C3H

Identifiers

PMID22135400
PMCPMC3273544

What OpenQuestion holds

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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.