Evidence map›Paper›PMID 23076626›Full record

ArticleBasic research in cardiology2012

Cardiac progenitors derived from reprogrammed mesenchymal stem cells contribute to angiomyogenic repair of the infarcted heart.

Stephanie Buccini, Khawaja Husnain Haider, Rafeeq P H Ahmed, Shujia Jiang, Muhammad Ashraf

Open access · hybridAbstract read
In one paragraph

Article in Basic research in cardiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 8% 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 118 citations in OpenAlex.

  1. Pooled it
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  9. Review
  10. Amniotic membrane as novel scaffold for human iPSC-derived cardiomyogenesis.In vitro cellular & developmental biology. Animal · 2019
    Article
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  20. Reprogramming approaches in cardiovascular regeneration.Current treatment options in cardiovascular medicine · 2014
    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

5 authors at 2 institutions in 1 country.

Stephanie BucciniDepartment of Pathology and Laboratory Medicine, University of Cincinnati, OH, 45267-0529, USA.
Khawaja Husnain Haider
Rafeeq P H Ahmed
Shujia Jiang
Muhammad Ashraf
Sabin Vaccine Institute · USUniversity of Cincinnati · US

Funding

Stem Cells in Cardiac Repair and AngiogenesisR37HL074272 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI ASHRAF, MUHAMMAD · 2003 to 2013
$5.7M
Angiomyogenesis With Myoblast Derived iPS CellsR01HL107957 · NHLBI · UNIVERSITY OF CINCINNATI · PI WANG, YIGANG · 2011 to 2015
$3.4M
Cardiac Repair Using Smart Stem CellsR01HL087246 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI ASHRAF, MUHAMMAD · 2007 to 2011
$2.8M
Angiomyogenesis with HIF-1a responsive microRNAsR01HL106190 · NHLBI · UNIVERSITY OF CINCINNATI · PI HABEEBAHMED, RAFEEQ · 2011 to 2016
$2.8M
Mechanistic basis of myoblast therapy &angiomyogenesisR01HL080686 · NHLBI · UNIVERSITY OF CINCINNATI · PI ASHRAF, MUHAMMAD · 2005 to 2009
$2.7M
Simltaneous recruitment of cardiac and bone marrow stem cells for cardiac repairR01HL089535 · NHLBI · UNIVERSITY OF CINCINNATI · PI HAIDER, KHAWAJA H · 2008 to 2012
$1.9M
Preconditioning and re-programming of stem cells for cardiac repairR01HL087288 · NHLBI · UNIVERSITY OF CINCINNATI · PI HABEEBAHMED, RAFEEQ, HAIDER, KHAWAJA H · 2008 to 2012
$1.9M
NHLBI NIH HHS HL-080686NHLBI NIH HHS HL-087246NHLBI NIH HHS HL-087288NHLBI NIH HHS HL-089535NHLBI NIH HHS HL-106190-01NHLBI NIH HHS HL-107957NHLBI NIH HHS R01 HL080686NHLBI NIH HHS R01 HL087246NHLBI NIH HHS R01 HL087288NHLBI NIH HHS R01 HL089535NHLBI NIH HHS R01 HL106190NHLBI NIH HHS R01 HL107957NHLBI NIH HHS R37 HL074272NHLBI NIH HHS R37-HL-074272
6 · The paper itself

Abstract

The strategy to reprogram somatic stem cells to pluripotency status has provided an alternative source of surrogate ES cells (ESC). We report efficient reprogramming of multipotent bone marrow (BM) mesenchymal stem cells (MSC) to pluripotent status and the resultant MSC derived iPS cells (MiPS) and their derived progenitors effectively repaired the infarcted heart. MSC from young, male, Oct4-GFP transgenic mice were reprogrammed by retroviral transduction with Oct4, Sox2, Klf4, and c-Myc stemness factors. MiPS thus generated displayed characteristics of mouse ESC including morphology, surface antigens, gene and miR expression profiles. MiPS also formed spontaneously beating cardiac progenitors which expressed cardiac specific transcription factors and protein markers including Gata4, Mef2c, Nkx2.5, myosin heavy chain, troponin-I, and troponin-T, and showed ultra structural characteristics typical of cardiomyocytes. Intramyocardial delivery of MiPS (group-2) and their derivative cardiac-like cells (MiPS-CP; group-3) in a mouse model of acute myocardial infarction showed extensive survival and engraftment at 4 weeks with resultant attenuation of infarct size (p < 0.001 vs. DMEM injected control; n = 4). Engraftment of MiPS-CP was without cardiac tumorigenesis as compared to 21 % in MiPS transplanted animals. Furthermore, angiogenesis was improved in groups-2 and 3 (p < 0.001 vs. control). Transthoracic echocardiography revealed significantly preserved indices of cardiac contractility (ejection fraction p < 0.001 and fractional shortening p < 0.001 vs. control; n = 7). MSC were successfully reprogrammed into MiPS that displayed ESC-like characteristics and differentiated into spontaneously beating cardiomyocytes. Cardiac progenitors derived from MiPS repopulated the infarcted heart without tumorigenesis and improved global cardiac function.

Indexed as

Cell DifferentiationAnimalsCell Transformation, NeoplasticHeart Function TestsInduced Pluripotent Stem CellsKruppel-Like Factor 4MaleMesenchymal Stem CellsMiceMice, TransgenicMicroRNAsMyocardial InfarctionMyocytes, CardiacNeovascularization, PhysiologicKlf4 protein, mouseKruppel-Like Factor 4MicroRNAs

Identifiers

PMID23076626
PMCPMC3505546
OpenAlexW2106326450

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.