Evidence map›Paper›PMID 31375001›Full record

ArticleInternational journal of molecular sciences2019

Compromised Barrier Function in Human Induced Pluripotent Stem-Cell-Derived Retinal Pigment Epithelial Cells from Type 2 Diabetic Patients.

Mostafa Kiamehr, Alexa Klettner, Elisabeth Richert, Ali Koskela, Arto Koistinen, Heli Skottman, Kai Kaarniranta, Katriina Aalto-Setälä, Kati Juuti-Uusitalo

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 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
5.9field-weighted citation impact, top 3% 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 44 citations in OpenAlex.

  1. The Hippo signalling pathway and its impact on eye diseases.Journal of cellular and molecular medicine · 2024
    Pooled it
  2. Autophagy in ocular diseases: from mechanisms to therapeutic potential.Frontiers in cell and developmental biology · 2026
    Review
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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

9 authors at 3 institutions in 3 countries.

Mostafa KiamehrFaculty of Medicine and Health Technology, Tampere University, 33014 Tampere, Finland.ORCID 0000-0003-1894-3237
Alexa KlettnerDepartment of Ophthalmology, University of Kiel, University Medical Center, 24105 Kiel, Germany.
Elisabeth RichertDepartment of Ophthalmology, University of Kiel, University Medical Center, 24105 Kiel, Germany.ORCID 0000-0002-1302-6651
Ali KoskelaDepartment of Ophthalmology, Institute of Clinical Medicine, University of Eastern Finland, 70210 Kuopio, Finland.
Arto KoistinenSIB Labs, University of Eastern Finland, 70210 Kuopio, Finland.ORCID 0000-0001-7601-9806
Heli SkottmanFaculty of Medicine and Health Technology, Tampere University, 33014 Tampere, Finland.
Kai KaarnirantaDepartment of Ophthalmology, Institute of Clinical Medicine, University of Eastern Finland, 70210 Kuopio, Finland.
Katriina Aalto-SetäläFaculty of Medicine and Health Technology, Tampere University, 33014 Tampere, Finland.
Kati Juuti-UusitaloFaculty of Medicine and Health Technology, Tampere University, 33014 Tampere, Finland.ORCID 0000-0003-2275-5562
Tampere University · FIUniversity of Eastern Finland · FIChristian-Albrechts-Universität zu Kiel · DE

Funding

Academy of Finland 218050, 139567Evald ja Hilda Nissi Stiftelse 2011, 2016Päivikki ja Sakari Sohlbergin Säätiö KaarnirantaTekes 2011undefined <span style="color:gray;font-size:10px;">undefined</span> 2012undefined <span style="color:gray;font-size:10px;">undefined</span> 2014, 2017undefined <span style="color:gray;font-size:10px;">undefined</span> Kaarniranta
6 · The paper itself

Abstract

In diabetic patients, high blood glucose induces alterations in retinal function and can lead to visual impairment due to diabetic retinopathy. In immortalized retinal pigment epithelial (RPE) cultures, high glucose concentrations are shown to lead to impairment in epithelial barrier properties. For the first time, the induced pluripotent stem-cell-derived retinal pigment epithelium (hiPSC-RPE) cell lines derived from type 2 diabetics and healthy control patients were utilized to assess the effects of glucose concentration on the cellular functionality. We show that both type 2 diabetic and healthy control hiPSC-RPE lines differentiate and mature well, both in high and normal glucose concentrations, express RPE specific genes, secrete pigment epithelium derived factor, and form a polarized cell layer. Here, type 2 diabetic hiPSC-RPE cells had a decreased barrier function compared to controls. Added insulin increased the epithelial cell layer tightness in normal glucose concentrations, and the effect was more evident in type 2 diabetics than in healthy control hiPSC-RPE cells. In addition, the preliminary functionality assessments showed that type 2 diabetic hiPSC-RPE cells had attenuated autophagy detected via ubiquitin-binding protein p62/Sequestosome-1 (p62/SQSTM1) accumulation, and lowered pro- matrix metalloproteinase 2 (proMMP2) as well as increased pro-MMP9 secretion. These results suggest that the cellular ability to tolerate stress is possibly decreased in type 2 diabetic RPE cells.

Indexed as

Cell LineCells, CulturedDiabetes Mellitus, Type 2Diabetic RetinopathyGlucoseHumansInduced Pluripotent Stem CellsPermeabilityRetinal Pigment EpitheliumGlucoseautophagybarrier functiondiabetic retinopathy (DR)induced pluripotent stem cells (hiPSC)matrix metalloproteinaseretinal pigment epithelial cellstype 2 diabetes

Identifiers

PMID31375001
PMCPMC6696227
OpenAlexW2965739774

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.