Evidence map›Paper›PMID 20694977›Full record

ArticleJournal of biomedical materials research. Part A2010

Fabrication of cardiac patch with decellularized porcine myocardial scaffold and bone marrow mononuclear cells.

Bo Wang, Ali Borazjani, Mina Tahai, Amy L de Jongh Curry, Dan T Simionescu, Jianjun Guan, Filip To, Steve H Elder, Jun Liao

Open access · bronzeAbstract read
In one paragraph

Article in Journal of biomedical materials research. Part A, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed, 1 pooled it
9.8field-weighted citation impact, top 2% 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

80 citing papers in PubMed, 1 synthesis or guideline pooled it, 165 citations in OpenAlex.

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  19. DYNAMIC BIOREACTOR MODEL TO MIMIC EARLY CARDIAC FIBROSIS IN DIABETES.Journal of mechanics in medicine and biology · 2021
    Article
  20. Review

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

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

9 authors at 4 institutions in 1 country.

Bo WangDepartment of Agricultural and Biological Engineering, Computational Manufacturing and Design, CAVS, Mississippi State University, Mississippi State, Mississippi, USA.
Ali Borazjani
Mina Tahai
Amy L de Jongh Curry
Dan T Simionescu
Jianjun Guan
Filip To
Steve H Elder
Jun Liao
Mississippi State University · USClemson University · USThe Ohio State University · USUniversity of Memphis · US

Funding

Tissue Engineered Aortic Heart Valves: Scaffolds and Stem CellsR01HL093399 · NHLBI · CLEMSON UNIVERSITY · PI SIMIONESCU, DAN TEODOR · 2010 to 2013
$1.4M
Tissue Engineered Cardiac Patches: Multifaceted Stimulation of Stem Cells in DeceR15HL097321 · NHLBI · MISSISSIPPI STATE UNIVERSITY · PI LIAO, JUN · 2009 to 2009
$205k
NHLBI NIH HHS HL097321NHLBI NIH HHS R01 HL093399NHLBI NIH HHS R15 HL097321PHS HHS R1CRH10429-01-00
6 · The paper itself

Abstract

Tissue engineered cardiac grafts are a promising therapeutic mode for ventricular wall reconstruction. Recently, it has been found that acellular tissue scaffolds provide natural ultrastructural, mechanical, and compositional cues for recellularization and tissue remodeling. We thus assess the potential of decellularized porcine myocardium as a scaffold for thick cardiac patch tissue engineering. Myocardial sections with 2-mm thickness were decellularized using 0.1% sodium dodecyl sulfate and then reseeded with differentiated bone marrow mononuclear cells. We found that thorough decellularization could be achieved after 2.5 weeks of treatment. Reseeded cells were found to infiltrate and proliferate in the tissue constructs. Immunohistological staining studies showed that the reseeded cells maintained cardiomyocyte-like phenotype and possible endothelialization was found in locations close to vasculature channels, indicating angiogenesis potential. Both biaxial and uniaxial mechanical testing showed a stiffer mechanical response of the acellular myocardial scaffolds; however, tissue extensibility and tensile modulus were found to recover in the constructs along with the culture time, as expected from increased cellular content. The cardiac patch that we envision for clinical application will benefit from the natural architecture of myocardial extracellular matrix, which has the potential to promote stem cell differentiation, cardiac regeneration, and angiogenesis.

Indexed as

AnimalsAnisotropyBone Marrow CellsCells, CulturedLeukocytes, MononuclearMechanical PhenomenaMyocardiumPhenotypePorositySarcomeresStaining and LabelingSus scrofaTissue EngineeringTissue Scaffolds

Identifiers

PMID20694977
PMCPMC2933781
OpenAlexW2097356835

What OpenQuestion holds

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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.