Evidence map›Paper›PMID 26651608›Full record

ArticleStem cell reports2015

Non-genetic Purification of Ventricular Cardiomyocytes from Differentiating Embryonic Stem Cells through Molecular Beacons Targeting IRX-4.

Kiwon Ban, Brian Wile, Kyu-Won Cho, Sangsung Kim, Ming-Ke Song, Sang Yoon Kim, Jason Singer, Anum Syed, Shan Ping Yu, Mary Wagner and 2 more

Open access · goldAbstract read
In one paragraph

Article in Stem cell reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

9 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Cardiomyocytes Derived from HumanScientific reports · 2018
    Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Probing early heart development to instruct stem cell differentiation strategies.Developmental dynamics : an official publication of the American Association of Anatomists · 2016
    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

12 authors at 3 institutions in 2 countries.

Kiwon BanDepartment of Medicine, Division of Cardiology, Emory University School of Medicine, Atlanta, GA 30322, USA.
Brian WileDepartment of Biomedical Engineering, Georgia Institute of Technology and Emory University, Atlanta, GA 30322, USA.
Kyu-Won ChoDepartment of Medicine, Division of Cardiology, Emory University School of Medicine, Atlanta, GA 30322, USA.
Sangsung KimDepartment of Medicine, Division of Cardiology, Emory University School of Medicine, Atlanta, GA 30322, USA.
Ming-Ke SongDepartment of Anesthesiology, Emory University School of Medicine, Atlanta, GA 30322, USA.
Sang Yoon KimDepartment of Medicine, Division of Cardiology, Emory University School of Medicine, Atlanta, GA 30322, USA.
Jason SingerDepartment of Pediatrics, Emory University School of Medicine and Children's Healthcare of Atlanta, Atlanta, GA 30322, USA.
Anum SyedDepartment of Biomedical Engineering, Georgia Institute of Technology and Emory University, Atlanta, GA 30322, USA.
Shan Ping YuDepartment of Anesthesiology, Emory University School of Medicine, Atlanta, GA 30322, USA.
Mary WagnerDepartment of Pediatrics, Emory University School of Medicine and Children's Healthcare of Atlanta, Atlanta, GA 30322, USA.
Gang BaoDepartment of Biomedical Engineering, Georgia Institute of Technology and Emory University, Atlanta, GA 30322, USA. Electronic address: gang.bao@rice.edu.
Young-Sup YoonDepartment of Medicine, Division of Cardiology, Emory University School of Medicine, Atlanta, GA 30322, USA; Severance Biomedical Science Institute, Yonsei University College of Medicine, Seoul 120-752, Korea. Electronic address: yyoon5@emory.edu.
Emory University · USGeorgia Institute of Technology · USChildren's Healthcare of Atlanta · US

Funding

Cell therapy for diabetic peripheral neurovascular complicationsDP3DK094346 · NIDDK · EMORY UNIVERSITY · PI CHENG, XIAODONG, YOON, YOUNG-SUP · 2011 to 2011
$6.1M
Excitation-contraction coupling in human ventricle developmentR01HL088488 · NHLBI · EMORY UNIVERSITY · PI WAGNER, MARY B · 2008 to 2012
$2.5M
Stem Cell-based therapy for LymphedemaR01HL127759 · NHLBI · EMORY UNIVERSITY · PI YOON, YOUNG-SUP · 2015 to 2018
$1.6M
Cardiac Regeneration with Bioengineered Human Stem CellsR01HL129511 · NHLBI · EMORY UNIVERSITY · PI YOON, YOUNG-SUP · 2016 to 2019
$1.6M
NHLBI NIH HHS HHSN268201000043CNHLBI NIH HHS R01 HL088488NHLBI NIH HHS R01HL088488NHLBI NIH HHS R01 HL127759NHLBI NIH HHS R01HL127759NHLBI NIH HHS R01 HL129511NIDDK NIH HHS DP3 DK094346NIDDK NIH HHS DP3DK094346
6 · The paper itself

Abstract

Isolation of ventricular cardiomyocytes (vCMs) has been challenging due to the lack of specific surface markers. Here we show that vCMs can be purified from differentiating mouse embryonic stem cells (mESCs) using molecular beacons (MBs) targeting specific intracellular mRNAs. We designed MBs (IRX4 MBs) to target mRNA encoding Iroquois homeobox protein 4 (Irx4), a transcription factor specific for vCMs. To purify mESC vCMs, IRX4 MBs were delivered into cardiomyogenically differentiating mESCs, and IRX4 MBs-positive cells were FACS-sorted. We found that, of the cells isolated, ~98% displayed vCM-like action potentials by electrophysiological analyses. These MB-purified vCMs continuously maintained their CM characteristics as verified by spontaneous beating, Ca(2+) transient, and expression of vCM-specific proteins. Our study shows the feasibility of isolating pure vCMs via cell sorting without modifying host genes. The homogeneous and functional ventricular CMs generated via the MB-based method can be useful for disease investigation, drug discovery, and cell-based therapies.

Indexed as

Action PotentialsAnimalsBase SequenceCell DifferentiationCells, CulturedCell SeparationEmbryonic Stem CellsFlow CytometryHeart VentriclesHomeodomain ProteinsMiceMyocytes, CardiacOligonucleotide ProbesRNA, MessengerHomeodomain ProteinsIrx4 protein, mouseOligonucleotide ProbesRNA, Messengercell selectionIRX4molecular beaconspluripotent stem cellventricular cardiomyocyte

Identifiers

PMID26651608
PMCPMC4682289
OpenAlexW2192043288

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.