Evidence map›Paper›PMID 37199081›Full record

ArticleFEBS open bio2024

Endothelial cell-derived extracellular vesicles induce pro-angiogenic responses in mesenchymal stem cells.

Hüseyin Abdik, Oğuz Kaan Kırbaş, Batuhan Turhan Bozkurt, Ezgi Avşar Abdik, Taha Bartu Hayal, Fikrettin Şahin, Pakize Neslihan Taşlı

Open access · goldAbstract read
In one paragraph

Article in FEBS open bio, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

7 authors at 3 institutions in 2 countries.

Hüseyin AbdikDepartment of Molecular Biology and Genetics, Faculty of Engineering and Natural Sciences, İstanbul Sabahattin Zaim University, Turkey.ORCID 0000-0003-3756-0645
Oğuz Kaan KırbaşDepartment of Genetics and Bioengineering, Faculty of Engineering and Architecture, Yeditepe University, Turkey.ORCID 0000-0002-7510-474X
Batuhan Turhan BozkurtDepartment of Genetics and Bioengineering, Faculty of Engineering and Architecture, Yeditepe University, Turkey.ORCID 0000-0003-1034-482X
Ezgi Avşar AbdikDepartment of Aquatic Genomics, Faculty of Aquatic Sciences, Istanbul University, Turkey.ORCID 0000-0003-0132-3234
Taha Bartu HayalDepartment of Genetics and Bioengineering, Faculty of Engineering and Architecture, Yeditepe University, Turkey.ORCID 0000-0003-1369-2715
Fikrettin ŞahinDepartment of Genetics and Bioengineering, Faculty of Engineering and Architecture, Yeditepe University, Turkey.ORCID 0000-0002-7208-8967
Pakize Neslihan TaşlıDepartment of Genetics and Bioengineering, Faculty of Engineering and Architecture, Yeditepe University, Turkey.ORCID 0000-0002-0455-9894
Yeditepe University · TRAquatic Systems (United States) · USİstanbul Sabahattin Zaim Üniversitesi · TR

Funding

Yeditepe University
6 · The paper itself

Abstract

Angiogenesis is a central component of vital biological processes such as wound healing, tissue nourishment, and development. Therefore, angiogenic activities are precisely maintained with secreted factors such as angiopoietin-1 (Ang1), fibroblast growth factor (FGF), and vascular endothelial growth factor (VEGF). As an element of intracellular communication, extracellular vesicles (EVs)-particularly EVs of vascular origin-could have key functions in maintaining angiogenesis. However, the functions of EVs in the control of angiogenesis have not been fully studied. In this study, human umbilical vein endothelial cell line (HUVEC)-derived small EVs (<200 nm; HU-sEVs) were investigated as a potential pro-angiogenic agent. Treating mesenchymal stem cells (MSCs) and mature HUVEC cells with HU-sEVs induced their tube formation under in vitro conditions and significantly increased the expression of angiogenesis-related genes, such as Ang1, VEGF, Flk-1 (VEGF receptor 2), Flt-1 (VEGF receptor 1), and vWF (von Willebrand Factor), in a dose-dependent manner. These results indicate that HU-sEVs take part in angiogenesis activities in physiological systems, and suggest endothelial EVs as a potential therapeutic candidate for the treatment of angiogenesis-related diseases.

Indexed as

Extracellular VesiclesHuman Umbilical Vein Endothelial CellsMesenchymal Stem CellsNeovascularization, PhysiologicAngiopoietin-1Cells, CulturedHumansVascular Endothelial Growth Factor AAngiopoietin-1Vascular Endothelial Growth Factor Aangiogenesisdifferentiationendothelial cellsexosomemesenchymal stem cellsmall extracellular vesicles

Identifiers

PMID37199081
PMCPMC11073499
OpenAlexW4377011396

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.