Evidence map›Paper›PMID 34375370›Full record

ArticlePloS one2021

Induced endothelial cells from peripheral arterial disease patients and neonatal fibroblasts have comparable angiogenic properties.

Jack D Hywood, Sara Sadeghipour, Zoe E Clayton, Jun Yuan, Colleen Stubbs, Jack W T Wong, John P Cooke, Sanjay Patel

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 56% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

8 authors at 4 institutions in 3 countries.

Jack D HywoodHeart Research Institute, Newtown, NSW, Australia.ORCID 0000-0002-2028-2629
Sara SadeghipourHeart Research Institute, Newtown, NSW, Australia.
Zoe E ClaytonHeart Research Institute, Newtown, NSW, Australia.
Jun YuanHeart Research Institute, Newtown, NSW, Australia.
Colleen StubbsRNACore, Houston Methodist Research Institute, Houston, Texas, United States of America.
Jack W T WongSchool of Life Sciences, Chinese University of Hong Kong, Hong Kong, China.
John P CookeDepartment of Cardiovascular Sciences, Houston Methodist Research Institute, Houston, Texas, United States of America.
Sanjay PatelHeart Research Institute, Newtown, NSW, Australia.
The University of Sydney · AUHouston Methodist · USThe Heart Research Institute · AUChinese University of Hong Kong · HK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Induced endothelial cells (iECs) generated from neonatal fibroblasts via transdifferentiation have been shown to have pro-angiogenic properties and are a potential therapy for peripheral arterial disease (PAD). It is unknown if iECs can be generated from fibroblasts collected from PAD patients and whether these cells are pro-angiogenic. In this study fibroblasts were collected from four PAD patients undergoing carotid endarterectomies. These cells, and neonatal fibroblasts, were transdifferentiated into iECs using modified mRNA. Endothelial phenotype and pro-angiogenic cytokine secretion were investigated. NOD-SCID mice underwent surgery to induce hindlimb ischaemia in a murine model of PAD. Mice received intramuscular injections with either control vehicle, or 1 × 106 neonatal-derived or 1 × 106 patient-derived iECs. Recovery in perfusion to the affected limb was measured using laser Doppler scanning. Perfusion recovery was enhanced in mice treated with neonatal-derived iECs and in two of the three patient-derived iEC lines investigated in vivo. Patient-derived iECs can be successfully generated from PAD patients and for specific patients display comparable pro-angiogenic properties to neonatal-derived iECs.

Indexed as

Neovascularization, PhysiologicAcetylationAnimalsCapillariesCell LineCell MovementCell TransdifferentiationCollagenCulture Media, ConditionedCytokinesDrug CombinationsEndothelial CellsFibroblastsHindlimbHumansInfant, NewbornCollagenCulture Media, ConditionedCytokinesDrug CombinationsIntercellular Signaling Peptides and ProteinsLamininLipoproteins, LDLmatrigelPlant LectinsProteoglycansUlex europaeus lectins

Identifiers

PMID34375370
PMCPMC8354451
OpenAlexW3187568121

What Socratic 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 Socratic graph.