Evidence map›Paper›PMID 33320624›Full record

ArticleACS biomaterials science & engineering2020

Preseeding of Mesenchymal Stem Cells Increases Integration of an iPSC-Derived CM Sheet into a Cardiac Matrix.

Pawan Kc, Mickey Shah, Rubia Shaik, Yi Hong, Ge Zhang

Open access · greenAbstract read
In one paragraph

Article in ACS biomaterials science & engineering, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Review
  3. Fibrin-Enriched Cardiac Extracellular Matrix Hydrogel PromotesACS biomaterials science & engineering · 2023
    Article
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.

Pawan KcDepartment of Biomedical Engineering, The University of Akron, Akron, Ohio 44325, United States.ORCID 0000-0001-7565-8948
Mickey ShahDepartment of Biomedical Engineering, The University of Akron, Akron, Ohio 44325, United States.ORCID 0000-0001-6374-5091
Rubia ShaikDepartment of Biomedical Engineering, The University of Akron, Akron, Ohio 44325, United States.
Yi HongDepartment of Bioengineering, University of Texas at Arlington, Arlington, Texas 76019, United States.ORCID 0000-0002-5846-2596
Ge ZhangDepartment of Biomedical Engineering, The University of Akron, Akron, Ohio 44325, United States.ORCID 0000-0001-8339-1892
University of Akron · USThe University of Texas at Arlington · US

Funding

Bioactive injectable blends for cardiac stem cell recruitmentR15HL140503 · NHLBI · UNIVERSITY OF TEXAS ARLINGTON · PI HONG, YI · 2018 to 2018
$460k
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 R15 HL140503
6 · The paper itself

Abstract

Cell sheet technology has demonstrated great promise in delivering a large amount of therapeutic cells for tissue repair, including in the myocardium. However, the lack of host integration remains one of the key challenges in using cell sheets for cardiac repair. Paracrine factors secreted by mesenchymal stem cells (MSCs) have been reported to facilitate tissue repair and regeneration in a variety of ways. It has been demonstrated that paracrine factors from MSCs could enhance scaffold recellularization and vascularization. In this study, we used an in vitro cardiac matrix mimic platform to examine the effects of hMSCs preseeding on the interactions between cell sheets and cardiac matrix. The fabricated human induced pluripotent stem cells-derived cardiomyocyte sheets were attached to a decellularized porcine myocardium slice with or without preseeding of hMSCs. The hMSCs preseeding significantly enhanced the interactions between cardiomyocyte sheets and cardiac matrix in terms of cell migration distance, cell distribution, and mature vascular and cardiomyocyte marker expressions in the matrix. Growth factor and matrix metalloproteinases array analysis suggested that hMSCs- induced vascularization and MMPs regulation are the two possible mechanisms that lead to the improved CMs and cardiac matrix interactions. Further examination of these two mechanisms will enable the development of new approaches to facilitate transplanted cells for tissue repair.

Indexed as

Induced Pluripotent Stem CellsMesenchymal Stem CellsAnimalsCell MovementHumansMyocardiumMyocytes, CardiacSwinecardiac matrixcell sheetdecellularized myocardiumhuman induced pluripotent stem cellsmesenchymal stem cells

Identifiers

PMID33320624
PMCPMC9841440
OpenAlexW3095055959

What OpenQuestion holds

Textmetadata
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.