Evidence map›Paper›PMID 21403094›Full record

ArticleCirculation2011

Human cardiac stem cell differentiation is regulated by a mircrine mechanism.

Toru Hosoda, Hanqiao Zheng, Mauricio Cabral-da-Silva, Fumihiro Sanada, Noriko Ide-Iwata, Barbara Ogórek, João Ferreira-Martins, Christian Arranto, Domenico D'Amario, Federica del Monte and 7 more

RetractedErratum issuedOpen access · greenAbstract readRetracted Publication
In one paragraph

Article in Circulation, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 99 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
99citing papers in PubMed, 2 pooled it
13.8field-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

99 citing papers in PubMed, 2 syntheses or guidelines pooled it, 201 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Direct Cardiac Reprogramming: A Novel Approach for Heart Regeneration.International journal of molecular sciences · 2018
    Review
  11. Article
  12. Exchange of genetic material: a new paradigm in bone cell communications.Cellular and molecular life sciences : CMLS · 2018
    Review
  13. Targeting miRNA for Therapy of Juvenile and Adult Diabetic Cardiomyopathy.Advances in experimental medicine and biology · 2018
    Article
  14. Article
  15. Deciphering Non-coding RNAs in Cardiovascular Health and Disease.Frontiers in cardiovascular medicine · 2018
    Review
  16. Article
  17. Review
  18. Review
  19. Article
  20. Review

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 1 institution in 1 country.

Toru HosodaDepartments of Anesthesia and Medicine, Brigham and Women’s Hospital, Harvard Medical School, 75 Francis St., Boston, MA 02115, USA. thosoda@partners.org
Hanqiao Zheng
Mauricio Cabral-da-Silva
Fumihiro Sanada
Noriko Ide-Iwata
Barbara Ogórek
João Ferreira-Martins
Christian Arranto
Domenico D'Amario
Federica del Monte
Konrad Urbanek
David A D'Alessandro
Robert E Michler
Piero Anversa
Marcello Rota
Jan Kajstura
Annarosa Leri
Beth Israel Deaconess Medical Center · US

Funding

Rebuilding the Failing HeartP01HL092868 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI ANVERSA, PIERO · 2008 to 2013
$12.9M
Stem Cells and Cardiac AgingP01AG023071 · NIA · NEW YORK MEDICAL COLLEGE · PI ANVERSA, PIERO · 2004 to 2008
$9.5M
Repair and Angiogenesis by Stem Cells in Human HeartR37HL081737 · NHLBI · NEW YORK MEDICAL COLLEGE · PI ANVERSA, PIERO · 2005 to 2015
$6.5M
IGF-1, Gender, Heart Failure and Longevity: A Paradigm ShiftR01AG017042 · NIA · NEW YORK MEDICAL COLLEGE · PI ANVERSA, PIERO · 2000 to 2010
$5.3M
Coronary Vasculature Progenitor Cell in Human Ischemic Heart FailureR01HL039902 · NHLBI · NEW YORK UNIVERSITY · PI ANVERSA, PIERO, KAJSTURA, JAN · 1989 to 2012
$4.7M
MYOCYTE STEM CELLS IN THE MAMMALIAN HEARTR01HL065577 · NHLBI · NEW YORK MEDICAL COLLEGE · PI LERI, ANNAROSA · 2000 to 2012
$2.9M
Stem Cells in the Developing HeartR01HL091021 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI ROTA, MARCELLO · 2009 to 2013
$2.4M
Redefining Human Myocardial BiologyR01HL105532 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI ANVERSA, PIERO, BUCHHOLZ, BRUCE A · 2011 to 2014
$2.2M
IGF-1 and Diabetic HeartR01HL065573 · NHLBI · NEW YORK MEDICAL COLLEGE · PI KAJSTURA, JAN · 2001 to 2010
$2.1M
Immortal DNA Strand and Cardiac Stem Cell AgingR01AG037495 · NIA · BRIGHAM AND WOMEN'S HOSPITAL · PI ANVERSA, PIERO · 2011 to 2014
$2.0M
Cardiac Stem Cell Growth, Aging and DeathR01HL075480 · NHLBI · NEW YORK MEDICAL COLLEGE · PI KAJSTURA, JAN · 2004 to 2008
$1.9M
Telomeric Shortening, p53 and miR-34a Condition Senescence of Cardiac ProgenitorsR01AG037490 · NIA · BRIGHAM AND WOMEN'S HOSPITAL · PI LERI, ANNAROSA · 2010 to 2014
$1.7M
NHLBI NIH HHS P01 HL092868NHLBI NIH HHS R01 HL039902NHLBI NIH HHS R01 HL065573NHLBI NIH HHS R01 HL065577NHLBI NIH HHS R01 HL075480NHLBI NIH HHS R01 HL091021NHLBI NIH HHS R01 HL105532NHLBI NIH HHS R01 HL111183NHLBI NIH HHS R21 HL094894NHLBI NIH HHS R37 HL081737NIA NIH HHS P01 AG023071NIA NIH HHS R01 AG017042NIA NIH HHS R01 AG037490NIA NIH HHS R01 AG037495
6 · The paper itself

Abstract

backgroundCardiac stem cells (CSCs) delivered to the infarcted heart generate a large number of small fetal-neonatal cardiomyocytes that fail to acquire the differentiated phenotype. However, the interaction of CSCs with postmitotic myocytes results in the formation of cells with adult characteristics. METHODS AND

resultsOn the basis of results of in vitro and in vivo assays, we report that the commitment of human CSCs (hCSCs) to the myocyte lineage and the generation of mature working cardiomyocytes are influenced by microRNA-499 (miR-499), which is barely detectable in hCSCs but is highly expressed in postmitotic human cardiomyocytes. miR-499 traverses gap junction channels and translocates to structurally coupled hCSCs favoring their differentiation into functionally competent cells. Expression of miR-499 in hCSCs represses the miR-499 target genes Sox6 and Rod1, enhancing cardiomyogenesis in vitro and after infarction in vivo. Although cardiac repair was detected in all cell-treated infarcted hearts, the aggregate volume of the regenerated myocyte mass and myocyte cell volume were greater in animals injected with hCSCs overexpressing miR-499. Treatment with hCSCs resulted in an improvement in ventricular function, consisting of a better preservation of developed pressure and positive and negative dP/dt after infarction. An additional positive effect on cardiac performance occurred with miR-499, pointing to enhanced myocyte differentiation/hypertrophy as the mechanism by which miR-499 potentiated the restoration of myocardial mass and function in the infarcted heart.

conclusionsThe recognition that miR-499 promotes the differentiation of hCSCs into mechanically integrated cardiomyocytes has important clinical implications for the treatment of human heart failure.

Indexed as

Stem Cell TransplantationAdult Stem CellsAnimalsCell DifferentiationCell DivisionCells, CulturedCoculture TechniquesDisease Models, AnimalGap JunctionsGene ExpressionHumansMicroRNAsMyocardial InfarctionMyocytes, CardiacPolypyrimidine Tract-Binding ProteinRatsMicroRNAsMIRN499 microRNA, humanMIRN499 microRNA, ratPolypyrimidine Tract-Binding ProteinPTBP3 protein, humanRNA-Binding ProteinsSOXD Transcription Factors

Identifiers

PMID21403094
PMCPMC3066266
OpenAlexW2135836706

What OpenQuestion holds

Textmetadata
LicenceTDM
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.