Evidence map›Paper›PMID 27488544›Full record

ArticleStem cell research & therapy2016

Significant improvement of direct reprogramming efficacy of fibroblasts into progenitor endothelial cells by ETV2 and hypoxia.

Phuc Van Pham, Ngoc Bich Vu, Hoa Trong Nguyen, Oanh Thuy Huynh, Mai Thi-Hoang Truong

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

20 citing papers in PubMed, 27 citations in OpenAlex.

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  8. Direct cell-fate conversion of somatic cells: Toward regenerative medicine and industries.Proceedings of the Japan Academy. Series B, Physical and biological sciences · 2020
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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 1 institution in 1 country.

Phuc Van PhamLaboratory of Stem Cell Research and Application, University of Science, Viet Nam National University, 227 Nguyen Van Cu, District 5, Ho Chi Minh City, Viet Nam. pvphuc@hcmuns.edu.vn.
Ngoc Bich VuLaboratory of Stem Cell Research and Application, University of Science, Viet Nam National University, 227 Nguyen Van Cu, District 5, Ho Chi Minh City, Viet Nam.
Hoa Trong NguyenLaboratory of Stem Cell Research and Application, University of Science, Viet Nam National University, 227 Nguyen Van Cu, District 5, Ho Chi Minh City, Viet Nam.
Oanh Thuy HuynhLaboratory of Stem Cell Research and Application, University of Science, Viet Nam National University, 227 Nguyen Van Cu, District 5, Ho Chi Minh City, Viet Nam.
Mai Thi-Hoang TruongLaboratory of Stem Cell Research and Application, University of Science, Viet Nam National University, 227 Nguyen Van Cu, District 5, Ho Chi Minh City, Viet Nam.
Vietnam National University Ho Chi Minh City · VN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEndothelial progenitor cell (EPC) transplantation is a promising therapy for ischemic diseases such as ischemic myocardial infarction and hindlimb ischemia. However, limitation of EPC sources remains a major obstacle. Direct reprogramming has become a powerful tool to produce EPCs from fibroblasts. Some recent efforts successfully directly reprogrammed human fibroblasts into functional EPCs; however, the procedure efficacy was low. This study therefore aimed to improve the efficacy of direct reprogramming of human fibroblasts to functional EPCs.

methodsHuman fibroblasts isolated from foreskin were directly reprogrammed into EPCs by viral ETV2 transduction. Reprogramming efficacy was improved by culturing transduced fibroblasts in hypoxia conditions (5 % oxygen). Phenotype analyses confirmed that single-factor ETV2 transduction successfully reprogrammed dermal fibroblasts into functional EPCs.

resultsHypoxia treatment during the reprogramming procedure increased the efficacy of reprogramming from 1.21 ± 0.61 % in normoxia conditions to 7.52 ± 2.31 % in hypoxia conditions. Induced EPCs in hypoxia conditions exhibited functional EPC phenotypes similar to those in normoxia conditions, such as expression of CD31 and VEGFR2, and expressed endothelial gene profiles similar to human umbilical vascular endothelial cells. These cells also formed capillary-like networks in vitro.

conclusionOur study demonstrates a new simple method to increase the reprogramming efficacy of human fibroblasts to EPCs using ETV2 and hypoxia.

Indexed as

Cell HypoxiaCells, CulturedCellular ReprogrammingEndothelial CellsEndothelial Progenitor CellsFibroblastsForeskinHumansHuman Umbilical Vein Endothelial CellsMalePlatelet Endothelial Cell Adhesion Molecule-1Transcription FactorsVascular Endothelial Growth Factor Receptor-2ETV2 protein, humanPlatelet Endothelial Cell Adhesion Molecule-1Transcription FactorsVascular Endothelial Growth Factor Receptor-2Direct reprogrammingEndothelial progenitor cellsEpigenetic reprogrammingETV2Fibroblast

Identifiers

PMID27488544
PMCPMC4973107
OpenAlexW2493685197

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.