Evidence map›Paper›PMID 30385769›Full record

ArticleScientific reports2018

A Thin Layer of Decellularized Porcine Myocardium for Cell Delivery.

Mickey Shah, Pawan Kc, Katherine M Copeland, Jun Liao, Ge Zhang

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

23 citing papers in PubMed, 32 citations in OpenAlex.

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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.

Mickey ShahIntegrated Bioscience Program, The University of Akron, Akron, OH, 44325-0302, USA.
Pawan KcDepartment of Biomedical Engineering, The University of Akron, Akron, OH, 44325-0302, USA.ORCID http://orcid.org/0000-0001-7565-8948
Katherine M CopelandDepartment of Bioengineering, University of Texas at Arlington, Arlington, Texas, 76019, USA.
Jun LiaoDepartment of Bioengineering, University of Texas at Arlington, Arlington, Texas, 76019, USA.ORCID http://orcid.org/0000-0003-1049-5783
Ge ZhangDepartment of Biomedical Engineering, The University of Akron, Akron, OH, 44325-0302, USA. gezhang@uakron.edu.
University of Akron · USThe University of Texas at Arlington · US

Funding

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
Reinforce Cell Sheets with Acellular Porcine Myocardial Scaffolds: Application in Cardiac RepairR15HL122949 · NHLBI · UNIVERSITY OF AKRON · PI ZHANG, GE · 2015 to 2015
$460k
NHLBI NIH HHS R15 HL122949NHLBI NIH HHS T32 HL134613NIBIB NIH HHS R01 EB022018
6 · The paper itself

Abstract

Decellularized porcine myocardium has shown many benefits as a cell delivery scaffold for cardiac therapy. However, using full thickness decellularized myocardium as cardiac patch may lead to poor viability and inhomogeneous distribution of delivered cells, due to perfusion limitations. In this study, we explored the feasibility of decellularized porcine myocardial slice (dPMS) to construct a vascularized cardiac patch for cell delivery. Decellularized porcine myocardium was sliced into thin layers (thickness~300 µm). Adipose-derived Stem cells (ASCs) obtained from rat and pig were seeded on dPMS. The viability, infiltration, and differentiation of seeded ASCs were examined. The mechanical properties of dPMSs of various thickness and native myocardium were tested. We noticed dPMS supported attachment and growth of rat and pig ASCs. Both rat and pig ASCs showed high viability, similar patterns of proliferation and infiltration within dPMS. Rat ASCs showed expression of early-endothelial markers followed by mature-endothelial marker without any additional inducers on dPMS. Using rat myocardial infarction model, we delivered ASCs using dPMS patched to the infarcted myocardium. After 1 week, a higher number of transplanted cells were present in the infarcted area when cells were delivered using dPMS versus direct injection. Compared with MI group, increased vascular formation was also observed.

Indexed as

Stem Cell TransplantationAdipocytesAnimalsCell DifferentiationHeartHumansMyocardial InfarctionStem CellsSwineTissue Scaffolds

Identifiers

PMID30385769
PMCPMC6212498
OpenAlexW2898328253

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.