Evidence map›Paper›PMID 25533939›Full record

ArticleJournal of molecular and cellular cardiology2015

A systematic analysis of neonatal mouse heart regeneration after apical resection.

Donald Marion Bryant, Caitlin Claire O'Meara, Nhi Ngoc Ho, Joseph Gannon, Lei Cai, Richard Theodore Lee

Open access · greenAbstract read
In one paragraph

Article in Journal of molecular and cellular cardiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed
5.8field-weighted citation impact, top 3% 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

71 citing papers in PubMed, 111 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. The role of periostin in cardiac fibrosis.Heart failure reviews · 2024
    Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. The regenerative capacity of neonatal tissues.Development (Cambridge, England) · 2022
    Review
  11. Review
  12. Review
  13. Article
  14. Review
  15. Review
  16. Review
  17. Article
  18. Review
  19. Apical Resection and Cryoinjury of Neonatal Mouse Heart.Methods in molecular biology (Clifton, N.J.) · 2021
    Article
  20. Review

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Donald Marion BryantCardiovascular Division, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Caitlin Claire O'MearaCardiovascular Division, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Nhi Ngoc HoCardiovascular Division, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Joseph GannonCardiovascular Division, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Lei CaiCardiovascular Division, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Richard Theodore LeeCardiovascular Division, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA; Harvard Stem Cell Institute, The Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02139, USA. Electronic address: RLee@Partners.org.
Harvard University · USBrigham and Women's Hospital · US

Funding

Cardiomyocyte Lineage and Turnover by Metabolic Fate-MappingR01AG040019 · NIA · BRIGHAM AND WOMEN'S HOSPITAL · PI LEE, RICHARD T · 2011 to 2015
$1.9M
Biasing Myocardial Neuregulin Signaling with Engineered LigandsR01HL117986 · NHLBI · HARVARD UNIVERSITY · PI LEE, RICHARD T · 2013 to 2016
$1.6M
Role of Nerves in Guiding Cardiac RegenerationF32HL117595 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI O'MEARA, CAITLIN C · 2013 to 2015
$124k
NHLBI NIH HHS F32 HL117595NHLBI NIH HHS HL117986NHLBI NIH HHS R01 HL117986NIA NIH HHS AG040019NIA NIH HHS R01 AG040019
6 · The paper itself

Abstract

The finding that neonatal mice are able to regenerate myocardium after apical resection has recently been questioned. We determined if heart regeneration is influenced by the size of cardiac resection and whether surgical retraction of the ventricular apex results in an increase in cardiomyocyte cell cycle activity. We performed moderate or large apical ventricular resections on neonatal mice and quantified scar infiltration into the left ventricular wall at 21 days post-surgery. Moderately resected hearts had 15±2% of the wall infiltrated by a collagen scar; significantly greater scar infiltration (23±4%) was observed in hearts with large resections. Resected hearts had higher levels of cardiomyocyte cell cycle activity relative to sham hearts. Surgically retracting the ventricle often resulted in fibrosis and induced cardiomyocyte cell cycle activity that were comparable to that of resected hearts. We conclude that apical resection in neonatal mice induces cardiomyocyte cell cycle activity and neomyogenesis, although scarring can occur. Surgical technique and definition of approach to assessing the extent of regeneration are both critical when using the neonatal mouse apical resection model.

Indexed as

Cardiac Surgical ProceduresAnimalsAnimals, NewbornCell CycleFibrosisHeartHeart VentriclesMiceMyocardiumMyocytes, CardiacRegenerationApical resectionCardiac regenerationFibrosisNeomyogenesis

Identifiers

PMID25533939
PMCPMC4302033
OpenAlexW2153812794

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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.