Evidence map›Paper›PMID 24386480›Full record

ArticlePloS one2013

Flk1+ and VE-cadherin+ endothelial cells derived from iPSCs recapitulates vascular development during differentiation and display similar angiogenic potential as ESC-derived cells.

Erin E Kohler, Kishore K Wary, Fei Li, Ishita Chatterjee, Norifumi Urao, Peter T Toth, Masuko Ushio-Fukai, Jalees Rehman, Changwon Park, Asrar B Malik

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.5field-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

21 citing papers in PubMed, 29 citations in OpenAlex.

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  8. Metabolic shift in density-dependent stem cell differentiation.Cell communication and signaling : CCS · 2017
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4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Erin E KohlerDepartment of Pharmacology and Center for Lung and Vascular Biology, The University of Illinois, Chicago, Illinois, United States of America.
Kishore K WaryDepartment of Pharmacology and Center for Lung and Vascular Biology, The University of Illinois, Chicago, Illinois, United States of America.
Fei LiDepartment of Pharmacology and Center for Lung and Vascular Biology, The University of Illinois, Chicago, Illinois, United States of America.
Ishita ChatterjeeDepartment of Pharmacology and Center for Lung and Vascular Biology, The University of Illinois, Chicago, Illinois, United States of America.
Norifumi UraoDepartment of Pharmacology and Center for Lung and Vascular Biology, The University of Illinois, Chicago, Illinois, United States of America.
Peter T TothResearch Resources Center, The University of Illinois, Chicago, Illinois, United States of America.
Masuko Ushio-FukaiDepartment of Pharmacology and Center for Lung and Vascular Biology, The University of Illinois, Chicago, Illinois, United States of America.
Jalees RehmanDepartment of Pharmacology and Center for Lung and Vascular Biology, The University of Illinois, Chicago, Illinois, United States of America ; Section of Cardiology, Department of Medicine, The University of Illinois, Chicago, Illinois, United States of America.
Changwon ParkDepartment of Pharmacology and Center for Lung and Vascular Biology, The University of Illinois, Chicago, Illinois, United States of America.
Asrar B MalikDepartment of Pharmacology and Center for Lung and Vascular Biology, The University of Illinois, Chicago, Illinois, United States of America.
University of Illinois Chicago · US

Funding

Mesenchymal-Endothelial Transition as a Homeostatic Regenerative Mechanism in Acute Lung InjuryR01HL090152 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI MALIK, ASRAR B., REHMAN, JALEES · 2007 to 2019
$5.9M
Regulation of Wnt Signaling by PAP2b During AngiogenesisR01HL079356 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI WARY, KISHORE K · 2006 to 2016
$3.0M
The role of mitochondria in embryonic stem cells.R01GM094220 · NIGMS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI REHMAN, JALEES · 2011 to 2015
$1.5M
Role of Cysteine Sulfenic Acid Formation in Compartmentalization of VEGF SignalinR21HL112293 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI USHIO-FUKAI, MASUKO · 2013 to 2014
$435k
NHLBI NIH HHS HL079356NHLBI NIH HHS HL090152NHLBI NIH HHS HL112293NHLBI NIH HHS R01 HL079356NHLBI NIH HHS R01 HL090152NHLBI NIH HHS R21 HL112293NIGMS NIH HHS GM094220NIGMS NIH HHS R01 GM094220
6 · The paper itself

Abstract

rationaleInduced pluripotent stem (iPS) cells have emerged as a source of potentially unlimited supply of autologous endothelial cells (ECs) for vascularization. However, the regenerative function of these cells relative to adult ECs and ECs derived from embryonic stem (ES) cells is unknown. The objective was to define the differentiation characteristics and vascularization potential of Fetal liver kinase (Flk)1(+) and Vascular Endothelial (VE)-cadherin(+) ECs derived identically from mouse (m)ES and miPS cells. METHODS AND

resultsNaive mES and miPS cells cultured in type IV collagen (IV Col) in defined media for 5 days induced the formation of adherent cell populations, which demonstrated similar expression of Flk1 and VE-cadherin and the emergence of EC progenies. FACS purification resulted in 100% Flk1(+) VE-cadherin(+) cells from both mES and miPS cells. Emergence of Flk1(+)VE-cadherin(+) cells entailed expression of the vascular developmental transcription factor Er71, which bound identically to Flk1, VE-cadherin, and CD31 promoters in both populations. Immunostaining with anti-VE-cadherin and anti-CD31 antibodies and microscopy demonstrated the endothelial nature of these cells. Each cell population (unlike mature ECs) organized into well-developed vascular structures in vitro and incorporated into CD31(+) neovessels in matrigel plugs implanted in nude mice in vivo.

conclusionThus, iPS cell-derived Flk1(+)VE-cadherin(+) cells expressing the Er71 are as angiogenic as mES cell-derived cells and incorporate into CD31(+) neovessels. Their vessel forming capacity highlights the potential of autologous iPS cells-derived EC progeny for therapeutic angiogenesis.

Indexed as

Gene Expression RegulationNeovascularization, PhysiologicAnimalsAntigens, CDCadherin 5CadherinsCell LineEndothelial CellsInduced Pluripotent Stem CellsMiceTranscription FactorsVascular Endothelial Growth Factor Receptor-2Antigens, CDCadherin 5CadherinsER71 protein, mouseTranscription FactorsVascular Endothelial Growth Factor Receptor-2

Identifiers

PMID24386480
PMCPMC3875577
OpenAlexW1989544046

What OpenQuestion holds

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Registered trials

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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.