Evidence map›Paper›PMID 26999719›Full record

ArticleJournal of cellular and molecular medicine2016

Oxidative stress in retinal pigment epithelium cells increases exosome secretion and promotes angiogenesis in endothelial cells.

Sandra Atienzar-Aroca, Miguel Flores-Bellver, Gemma Serrano-Heras, Natalia Martinez-Gil, Jorge M Barcia, Silvia Aparicio, Daniel Perez-Cremades, Jose M Garcia-Verdugo, Manuel Diaz-Llopis, Francisco J Romero and 1 more

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 140 papers.

0numbers the graph read from it
0cells of the map it votes in
140citing papers in PubMed
10.8field-weighted citation impact, top 1% 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

140 citing papers in PubMed, 230 citations in OpenAlex.

  1. Article
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  4. Article
  5. Niche-derived exosomes controlFrontiers in immunology · 2026
    Article
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80 more citing papers are in PubMed but not listed here.

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

11 authors at 5 institutions in 2 countries.

Sandra Atienzar-ArocaSchool of Medicine, Catholic University of Valencia, Valencia, Spain.
Miguel Flores-BellverSchool of Medicine, Catholic University of Valencia, Valencia, Spain.
Gemma Serrano-HerasExperimental Research Unit, General University Hospital of Albacete, Albacete, Spain.
Natalia Martinez-GilSchool of Medicine, Catholic University of Valencia, Valencia, Spain.
Jorge M BarciaSchool of Medicine, Catholic University of Valencia, Valencia, Spain.
Silvia AparicioValencian Biomedicine Institute CSIC, Valencia, Spain.
Daniel Perez-CremadesDepartment of Physiology, University of Valencia, Valencia, Spain.
Jose M Garcia-VerdugoDepartment of Comparative Neurobiology, Cavanilles Institute of Biodiversity and Evolutive Biology, University of Valencia, Paterna, Valencia, Spain.
Manuel Diaz-LlopisDepartment of Surgery, University of Valencia, Valencia, Spain.
Francisco J RomeroSchool of Medicine, Catholic University of Valencia, Valencia, Spain.
Javier Sancho-PelluzSchool of Medicine, Catholic University of Valencia, Valencia, Spain.
Universitat de València · ESHospital General Universitario de Albacete · ESInstituto de Biomedicina de Valencia · ESParc Científic de la Universitat de València · ESValencia Catholic University Saint Vincent Martyr · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The retinal pigment epithelium (RPE), a monolayer located between the photoreceptors and the choroid, is constantly damaged by oxidative stress, particularly because of reactive oxygen species (ROS). As the RPE, because of its physiological functions, is essential for the survival of the retina, any sustained damage may consequently lead to loss of vision. Exosomes are small membranous vesicles released into the extracellular medium by numerous cell types, including RPE cells. Their cargo includes genetic material and proteins, making these vesicles essential for cell-to-cell communication. Exosomes may fuse with neighbouring cells influencing their fate. It has been observed that RPE cells release higher amounts of exosomes when they are under oxidative stress. Exosomes derived from cultured RPE cells were isolated by ultracentrifugation and quantified by flow cytometry. VEGF receptors (VEGFR) were analysed by both flow cytometry and Western blot. RT-PCR and qPCR were conducted to assess mRNA content of VEGFRs in exosomes. Neovascularization assays were performed after applying RPE exosomes into endothelial cell cultures. Our results showed that stressed RPE cells released a higher amount of exosomes than controls, with a higher expression of VEGFR in the membrane, and enclosed an extra cargo of VEGFR mRNA. Angiogenesis assays confirmed that endothelial cells increased their tube formation capacity when exposed to stressed RPE exosomes.

Indexed as

Neovascularization, PhysiologicOxidative StressCell LineEthanolExosomesHumansHuman Umbilical Vein Endothelial CellsReceptors, Vascular Endothelial Growth FactorRetinal Pigment EpitheliumRNA, MessengerVascular Endothelial Growth Factor AEthanolReceptors, Vascular Endothelial Growth FactorRNA, MessengerVascular Endothelial Growth Factor Aangiogenesisexosomesoxidative stressretinal pigment epitheliumVEGF receptors

Identifiers

PMID26999719
PMCPMC4956947
OpenAlexW2308533514

What OpenQuestion holds

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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.