Evidence map›Paper›PMID 22275487›Full record

ArticleCirculation research2012

Cardiomyogenesis in the developing heart is regulated by c-kit-positive cardiac stem cells.

João Ferreira-Martins, Barbara Ogórek, Donato Cappetta, Alex Matsuda, Sergio Signore, Domenico D'Amario, James Kostyla, Elisabeth Steadman, Noriko Ide-Iwata, Fumihiro Sanada and 7 more

RetractedOpen access · greenAbstract readRetracted Publication
In one paragraph

Article in Circulation research, 2012. 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 It has been retracted, and should not be counted.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 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
9.0field-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

54 citing papers in PubMed, 106 citations in OpenAlex.

  1. Unravelling the Interplay between Cardiac Metabolism and Heart Regeneration.International journal of molecular sciences · 2023
    Review
  2. Article
  3. Bradykinin-mediated CaJournal of cellular and molecular medicine · 2018
    Article
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  20. cKit+ cardiac progenitors of neural crest origin.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 1 institution in 2 countries.

João Ferreira-MartinsDepartment of Anesthesia, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Barbara Ogórek
Donato Cappetta
Alex Matsuda
Sergio Signore
Domenico D'Amario
James Kostyla
Elisabeth Steadman
Noriko Ide-Iwata
Fumihiro Sanada
Grazia Iaffaldano
Sergio Ottolenghi
Toru Hosoda
Annarosa Leri
Jan Kajstura
Piero Anversa
Marcello Rota
Norwegian Womens Public Health Association · NO

Funding

Rebuilding the Failing HeartP01HL092868 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI ANVERSA, PIERO · 2008 to 2013
$12.9M
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
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
Cardiac Stem Cells and AngiomyogenesisR01HL111183 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI LERI, ANNAROSA · 2012 to 2015
$1.7M
Aging and Homeostasis of Cardiac Stem Cell NichesR01AG026107 · NIA · NEW YORK MEDICAL COLLEGE · PI LERI, ANNAROSA · 2006 to 2010
$1.7M
NHLBI NIH HHS P01 HL092868NHLBI 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 R37 HL081737NIA NIH HHS R01 AG017042NIA NIH HHS R01 AG026107NIA NIH HHS R01 AG037490NIA NIH HHS R01 AG037495
6 · The paper itself

Abstract

rationaleEmbryonic and fetal myocardial growth is characterized by a dramatic increase in myocyte number, but whether the expansion of the myocyte compartment is dictated by activation and commitment of resident cardiac stem cells (CSCs), division of immature myocytes or both is currently unknown.

objectiveIn this study, we tested whether prenatal cardiac development is controlled by activation and differentiation of CSCs and whether division of c-kit-positive CSCs in the mouse heart is triggered by spontaneous Ca(2+) oscillations. METHODS AND

resultsWe report that embryonic-fetal c-kit-positive CSCs are self-renewing, clonogenic and multipotent in vitro and in vivo. The growth and commitment of c-kit-positive CSCs is responsible for the generation of the myocyte progeny of the developing heart. The close correspondence between values computed by mathematical modeling and direct measurements of myocyte number at E9, E14, E19 and 1 day after birth strongly suggests that the organogenesis of the embryonic heart is dependent on a hierarchical model of cell differentiation regulated by resident CSCs. The growth promoting effects of c-kit-positive CSCs are triggered by spontaneous oscillations in intracellular Ca(2+), mediated by IP3 receptor activation, which condition asymmetrical stem cell division and myocyte lineage specification.

conclusionsMyocyte formation derived from CSC differentiation is the major determinant of cardiac growth during development. Division of c-kit-positive CSCs in the mouse is promoted by spontaneous Ca(2+) spikes, which dictate the pattern of stem cell replication and the generation of a myocyte progeny at all phases of prenatal life and up to one day after birth.

Indexed as

AnimalsCalciumCalcium SignalingCell DifferentiationCells, CulturedEmbryo Culture TechniquesEmbryonic Stem CellsHeartInositol 1,4,5-Trisphosphate ReceptorsMiceMice, Inbred C57BLMice, TransgenicModels, AnimalModels, TheoreticalMyocytes, CardiacOrganogenesisCalciumInositol 1,4,5-Trisphosphate ReceptorsProto-Oncogene Proteins c-kit

Identifiers

PMID22275487
PMCPMC3292662
OpenAlexW2102525690

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.