Evidence map›Paper›PMID 36004926›Full record

ArticleBioengineering (Basel, Switzerland)2022

Investigating the Transient Regenerative Potential of Cardiac Muscle Using a Neonatal Pig Partial Apical Resection Model.

Katherine M Copeland, Bryn L Brazile, J Ryan Butler, Jim Cooley, Erin Brinkman-Ferguson, Andrew Claude, Sallie Lin, Sammira Rais-Rohani, Bradley Welch, Sara R McMahan and 7 more

Open access · goldAbstract read
In one paragraph

Article in Bioengineering (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 48% 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

4 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
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

17 authors at 5 institutions in 1 country.

Katherine M CopelandDepartment of Bioengineering, University of Texas at Arlington, Arlington, TX 76010, USA.
Bryn L BrazileDepartment of Biological Engineering, College of Veterinary Medicine, Mississippi State University, Starkville, MS 39762, USA.
J Ryan ButlerDepartment of Biological Engineering, College of Veterinary Medicine, Mississippi State University, Starkville, MS 39762, USA.
Jim CooleyDepartment of Biological Engineering, College of Veterinary Medicine, Mississippi State University, Starkville, MS 39762, USA.ORCID 0000-0002-9474-9922
Erin Brinkman-FergusonDepartment of Biological Engineering, College of Veterinary Medicine, Mississippi State University, Starkville, MS 39762, USA.
Andrew ClaudeDepartment of Biological Engineering, College of Veterinary Medicine, Mississippi State University, Starkville, MS 39762, USA.
Sallie LinDepartment of Biological Engineering, College of Veterinary Medicine, Mississippi State University, Starkville, MS 39762, USA.
Sammira Rais-RohaniDepartment of Biological Engineering, College of Veterinary Medicine, Mississippi State University, Starkville, MS 39762, USA.
Bradley WelchDepartment of Biological Engineering, College of Veterinary Medicine, Mississippi State University, Starkville, MS 39762, USA.
Sara R McMahanDepartment of Bioengineering, University of Texas at Arlington, Arlington, TX 76010, USA.
Kytai T NguyenDepartment of Bioengineering, University of Texas at Arlington, Arlington, TX 76010, USA.
Yi HongDepartment of Bioengineering, University of Texas at Arlington, Arlington, TX 76010, USA.ORCID 0000-0002-5846-2596
Sharan RamaswamyDepartment of Biomedical Engineering, Florida International University, Miami, FL 33174, USA.ORCID 0000-0003-4108-7141
Zhi-Ping LiuDepartment of Cardiovascular and Thoracic Surgery, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Pietro BajonaDepartment of Cardiovascular and Thoracic Surgery, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Matthias PeltzDepartment of Cardiovascular and Thoracic Surgery, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.ORCID 0000-0002-7384-252X
Jun LiaoDepartment of Bioengineering, University of Texas at Arlington, Arlington, TX 76010, USA.ORCID 0000-0003-1049-5783
Mississippi State University · USThe University of Texas at Arlington · USThe University of Texas Southwestern Medical Center · USAllegheny Health Network · USFlorida International University · US

Funding

Role of Cilp1 in Post-Natal Heart Response to InjuryR01HL157050 · NHLBI · UT SOUTHWESTERN MEDICAL CENTER · PI LIU, ZHI-PING · 2022 to 2025
$2.2M
Targeting KDM4B, a novel alternative splicing regulator, in castration-resistant prostate cancer (CRPC)R01CA215063 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI HSIEH, JER-TSONG, LIU, ZHI-PING · 2018 to 2022
$1.9M
Interdisciplinary Training in Nanotechnology for Cardiovascular and Lung Diseases in North TexasT32HL134613 · NHLBI · UNIVERSITY OF TEXAS ARLINGTON · PI NGUYEN, KYTAI TRUONG · 2017 to 2021
$1.1M
CONTROL OF CARDIAC FIBROSIS TO PREVENT CARDIAC FUNCTION DETERIORATIONR01EB022018 · NIBIB · WASHINGTON UNIVERSITY · PI GUAN, JIANJUN · 2016 to 2018
$1.1M
Bioactive injectable blends for cardiac stem cell recruitmentR15HL140503 · NHLBI · UNIVERSITY OF TEXAS ARLINGTON · PI HONG, YI · 2018 to 2018
$460k
A Controlled Septal Ablation for Inoperable Hypertrophic CardiomyopathyR15HL159599 · NHLBI · UNIVERSITY OF TEXAS ARLINGTON · PI LIAO, JUN · 2022 to 2022
$433k
NCI NIH HHS R01 CA215063NHLBI NIH HHS R01 HL157050NHLBI NIH HHS R15 HL140503NHLBI NIH HHS R15 HL159599NHLBI NIH HHS T32 HL134613NIBIB NIH HHS R01 EB022018NIH HHS R01HL157050; R01EB022018; T32HL134613
6 · The paper itself

Abstract

Researchers have shown that adult zebrafish have the potential to regenerate 20% of the ventricular muscle within two months of apex resection, and neonatal mice have the capacity to regenerate their heart after apex resection up until day 7 after birth. The goal of this study was to determine if large mammals (porcine heart model) have the capability to fully regenerate a resected portion of the left ventricular apex during the neonatal stage, and if so, how long the regenerative potential persists. A total of 36 piglets were divided into the following groups: 0-day control and surgical groups and seven-day control and surgical groups. For the apex removal groups, each piglet was subjected to a partial wall thickness resection (~30% of the ventricular wall thickness). Heart muscle function was assessed via transthoracic echocardiograms; the seven-day surgery group experienced a decrease in ejection fraction and fractional shortening. Upon gross necropsy, for piglets euthanized four weeks post-surgery, all 0-day-old hearts showed no signs of scarring or any indication of the induced injury. Histological analysis confirmed that piglets in the 0-day surgery group exhibited various degrees of regeneration, with half of the piglets showing full regeneration and the other half showing partial regeneration. However, each piglet in the seven-day surgery group demonstrated epicardial fibrosis along with moderate to severe dissecting interstitial fibrosis, which was accompanied by an abundant collagenous extracellular matrix as the result of a scar formation in the resection site. Histology of one 0-day apex resection piglet (briefly lain on and accidentally killed by the mother sow three days post-surgery) revealed dense, proliferative mesenchymal cells bordering the fibrin and hemorrhage zone and differentiating toward immature cardiomyocytes. We further examined the heart explants at 5-days post-surgery (5D PO) and 1-week post-surgery (1W PO) to assess the repair progression. For the 0-day surgery piglets euthanized at 5D PO and 1W PO, half had abundant proliferating mesenchymal cells, suggesting active regeneration, while the other half showed increased extracellular collagen. The seven-day surgery piglets euthanized at 5D PO, and 1W PO showed evidence of greatly increased extracellular collagen, while some piglets had proliferating mesenchymal cells, suggesting a regenerative effort is ongoing while scar formation seems to predominate. In short, our qualitative findings suggest that the piglets lose the full myocardial regenerative potential by 7 days after birth, but greatly preserve the regenerative potential within 1 day post-partum.

Indexed as

cardiac fibrosiscardiomyocytesneonatal pig heartpartial apex resectionproliferative mesenchymal cellstransient cardiac regeneration

Identifiers

PMID36004926
PMCPMC9404987
OpenAlexW4293105853

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.