Evidence map›Paper›PMID 28545044›Full record

ArticlePloS one2017

Differentiation of spontaneously contracting cardiomyocytes from non-virally reprogrammed human amniotic fluid stem cells.

Aaron J Velasquez-Mao, Christopher J M Tsao, Madeline N Monroe, Xavier Legras, Beatrice Bissig-Choisat, Karl-Dimiter Bissig, Rodrigo Ruano, Jeffrey G Jacot

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

14 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
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  7. Article
  8. Review
  9. Amniotic Fluid Cells, Stem Cells, and p53: Can We Stereotype p53 Functions?International journal of molecular sciences · 2019
    Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Bioengineering Cardiac Tissue Constructs With Adult Rat Cardiomyocytes.ASAIO journal (American Society for Artificial Internal Organs : 1992)
    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

8 authors at 3 institutions in 1 country.

Aaron J Velasquez-MaoDepartment of Bioengineering, Rice University, Houston, TX, United States of America.
Christopher J M TsaoDepartment of Bioengineering, Rice University, Houston, TX, United States of America.ORCID http://orcid.org/0000-0003-0341-3196
Madeline N MonroeDepartment of Bioengineering, Rice University, Houston, TX, United States of America.
Xavier LegrasDepartment of Molecular and Cellular Biology, Center for Cell and Gene Therapy, Stem Cells and Regenerative Medicine Center, Baylor College of Medicine, Houston, TX, United States of America.
Beatrice Bissig-ChoisatDepartment of Molecular and Cellular Biology, Center for Cell and Gene Therapy, Stem Cells and Regenerative Medicine Center, Baylor College of Medicine, Houston, TX, United States of America.
Karl-Dimiter BissigDepartment of Molecular and Cellular Biology, Center for Cell and Gene Therapy, Stem Cells and Regenerative Medicine Center, Baylor College of Medicine, Houston, TX, United States of America.
Rodrigo RuanoDepartment of Obstetrics and Gynecology, Maternal Fetal Medicine Texas Children's Hospital, Houston, TX, United States of America.
Jeffrey G JacotDepartment of Bioengineering, Rice University, Houston, TX, United States of America.
Baylor College of Medicine · USRice University · USTexas Children's Hospital · US

Funding

Therapeutic potential of CRISPR/Cas9 genome engineering in humanized mouse modelsR01HL134510 · NHLBI · DUKE UNIVERSITY · PI BISSIG, KARL-DIMITER · 2016 to 2020
$3.0M
PRE-VASCULARIZED AND DEGRADABLE PATCHES FOR CORRECTION OF CONGENITAL HEART DEFECTSR01HL130436 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI JACOT, JEFFREY G · 2016 to 2020
$2.0M
NHLBI NIH HHS R01 HL130436NHLBI NIH HHS R01 HL134510
6 · The paper itself

Abstract

Congenital heart defects are the most common birth defect. The limiting factor in tissue engineering repair strategies is an autologous source of functional cardiomyocytes. Amniotic fluid contains an ideal cell source for prenatal harvest and use in correction of congenital heart defects. This study aims to investigate the potential of amniotic fluid-derived stem cells (AFSC) to undergo non-viral reprogramming into induced pluripotent stem cells (iPSC) followed by growth-factor-free differentiation into functional cardiomyocytes. AFSC from human second trimester amniotic fluid were transfected by non-viral vesicle fusion with modified mRNA of OCT4, KLF4, SOX2, LIN28, cMYC and nuclear GFP over 18 days, then differentiated using inhibitors of GSK3 followed 48 hours later by inhibition of WNT. AFSC-derived iPSC had high expression of OCT4, NANOG, TRA-1-60, and TRA-1-81 after 18 days of mRNA transfection and formed teratomas containing mesodermal, ectodermal, and endodermal germ layers in immunodeficient mice. By Day 30 of cardiomyocyte differentiation, cells contracted spontaneously, expressed connexin 43 and β-myosin heavy chain organized in sarcomeric banding patterns, expressed cardiac troponin T and β-myosin heavy chain, showed upregulation of NKX2.5, ISL-1 and cardiac troponin T with downregulation of POU5F1, and displayed calcium and voltage transients similar to those in developing cardiomyocytes. These results demonstrate that cells from human amniotic fluid can be differentiated through a pluripotent state into functional cardiomyocytes.

Indexed as

Amniotic FluidAnimalsAntigens, SurfaceCell DifferentiationCells, CulturedCellular ReprogrammingFemaleFetal Stem CellsHumansInduced Pluripotent Stem CellsKruppel-Like Factor 4MiceMyocytes, CardiacNanog Homeobox ProteinOctamer Transcription Factor-3PregnancyAntigens, SurfaceKLF4 protein, humanKlf4 protein, mouseKruppel-Like Factor 4Nanog Homeobox ProteinNANOG protein, humanOctamer Transcription Factor-3POU5F1 protein, humanProteoglycansTRA-1-60 antigen, humanTRA-1-81 antigen, human

Identifiers

PMID28545044
PMCPMC5435315
OpenAlexW2615737076

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.