Evidence map›Paper›PMID 30791639›Full record

ArticleInternational journal of molecular sciences2019

Human Embryonic Stem Cell-Derived Retinal Pigment Epithelium-Role in Dead Cell Clearance and Inflammation.

Mária Szatmári-Tóth, Tanja Ilmarinen, Alexandra Mikhailova, Heli Skottman, Anu Kauppinen, Kai Kaarniranta, Endre Kristóf, Lyubomyr Lytvynchuk, Zoltán Veréb, László Fésüs and 1 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 23% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

  1. Pooled it
  2. Monitoring Gene Expression in Retina with synthetic serum markers.bioRxiv : the preprint server for biology · 2026
    Article
  3. Article
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  6. Article
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  8. Article
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  10. Article
  11. Article
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  14. Article
  15. The Role of Autophagy in Eye Diseases.Life (Basel, Switzerland) · 2021
    Review
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  17. Review
  18. 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

11 authors at 6 institutions in 4 countries.

Mária Szatmári-TóthDepartment of Biochemistry and Molecular Biology, University of Debrecen, Faculty of Medicine, 4032 Debrecen, Hungary. szatmari-toth.maria@med.unideb.hu.
Tanja IlmarinenTampere University, Faculty of Medicine and Health Technology, 33014 Tampere, Finland. tanja.ilmarinen@tuni.fi.
Alexandra MikhailovaTampere University, Faculty of Medicine and Health Technology, 33014 Tampere, Finland. alex.mikhailova@gmail.com.ORCID 0000-0003-2598-8353
Heli SkottmanTampere University, Faculty of Medicine and Health Technology, 33014 Tampere, Finland. heli.skottman@tuni.fi.
Anu KauppinenSchool of Pharmacy, Faculty of Health Sciences, University of Eastern Finland, 70211 Kuopio, Finland. anu.kauppinen@uef.fi.ORCID 0000-0001-8254-0200
Kai KaarnirantaDepartment of Ophthalmology, Institute of Clinical Medicine, University of Eastern Finland, 70211 Kuopio, Finland. kai.kaarniranta@kuh.fi.ORCID 0000-0003-2600-8679
Endre KristófDepartment of Biochemistry and Molecular Biology, University of Debrecen, Faculty of Medicine, 4032 Debrecen, Hungary. kristof.endre@med.unideb.hu.ORCID 0000-0002-2215-6984
Lyubomyr LytvynchukDepartment of Ophthalmology, Justus-Liebig-University Giessen, Eye Clinic, University Hospital Giessen and Marburg GmbH, Campus Giessen, 35390 Giessen, Germany. Lyubomyr.Lytvynchuk@augen.med.uni-giessen.de.
Zoltán VerébDepartment of Ophthalmology, Faculty of Medicine, University of Szeged, 6720 Szeged, Hungary. vereb.zoltan@med.u-szeged.hu.
László FésüsDepartment of Biochemistry and Molecular Biology, University of Debrecen, Faculty of Medicine, 4032 Debrecen, Hungary. fesus@med.unideb.hu.
Goran PetrovskiDepartment of Biochemistry and Molecular Biology, University of Debrecen, Faculty of Medicine, 4032 Debrecen, Hungary. goran.petrovski@medisin.uio.no.
Tampere University · FIUniversity of Debrecen · HUUniversity of Eastern Finland · FIJustus-Liebig-Universität Gießen · DEOslo University Hospital · NOUniversity of Szeged · HU

Funding

Academy of Finland grant numbers: 218050 and 133879ÚNKP-17-4 New National Excellence Program of the Ministry of Human Capacities of Hungary, TÁMOP-4.2.2.A-11/1/KONV-2012-0023, TÁMOP-4.2.2. A-11/1/KONV-2012-0025 grant, the National Brain Research Program (KTIA_NAP_13-A_III/9), as well as the GINOP-2.3.2-15 ÚNKP-17-4 New National Excellence Program of the Ministry of Human Capacities of Hungary, TÁMOP-4.2.2.A-11/1/KONV-2012-0023, TÁMOP-4.2.2. A-11/1/KONV-2012-0025 grant, the National Brain Research Program (KTIA_NAP_13-A_III/9), as well as the GINOP-2.3.2-15
6 · The paper itself

Abstract

Inefficient removal of dying retinal pigment epithelial (RPE) cells by professional phagocytes can result in debris formation and development of age-related macular degeneration (AMD). Chronic oxidative stress and inflammation play an important role in AMD pathogenesis. Only a few well-established in vitro phagocytosis assay models exist. We propose human embryonic stem cell-derived-RPE cells as a new model for studying RPE cell removal by professional phagocytes. The characteristics of human embryonic stem cells-derived RPE (hESC-RPE) are similar to native RPEs based on their gene and protein expression profile, integrity, and barrier properties or regarding drug transport. However, no data exist about RPE death modalities and how efficiently dying hESC-RPEs are taken upby macrophages, and whether this process triggers an inflammatory responses. This study demonstrates hESC-RPEs can be induced to undergo anoikis or autophagy-associated cell death due to extracellular matrix detachment or serum deprivation and hydrogen-peroxide co-treatment, respectively, similar to primary human RPEs. Dying hESC-RPEs are efficiently engulfed by macrophages which results in high amounts of IL-6 and IL-8 cytokine release. These findings suggest that the clearance of anoikic and autophagy-associated dying hESC-RPEs can be used as a new model for investigating AMD pathogenesis or for testing the in vivo potential of these cells in stem cell therapy.

Indexed as

AutophagyBiomarkersCell DifferentiationCell SurvivalCytokinesExtracellular MatrixHuman Embryonic Stem CellsHumansHydrogen PeroxideImmunophenotypingInflammationInflammation MediatorsMacrophagesMacular DegenerationOxidative StressPhagocytosisBiomarkersCytokinesHydrogen PeroxideInflammation Mediatorsage-related macular degenerationanoikisautophagyhESC-RPEinflammationmacrophagesphagocytosistriamcinolone

Identifiers

PMID30791639
PMCPMC6412543
OpenAlexW2917201807

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.