Evidence map›Paper›PMID 34360894›Full record

ArticleInternational journal of molecular sciences2021

Relative Contribution of Different Mitochondrial Oxidative Phosphorylation Components to the Retinal Pigment Epithelium Barrier Function: Implications for RPE-Related Retinal Diseases.

Michael H Guerra, Thangal Yumnamcha, Lalit P Singh, Ahmed S Ibrahim

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
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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

4 authors at 2 institutions in 2 countries.

Michael H GuerraDepartment of Ophthalmology, Visual and Anatomical Sciences, School of Medicine, Wayne State University, 540 East Canfield, Detroit, MI 48201, USA.
Thangal YumnamchaDepartment of Ophthalmology, Visual and Anatomical Sciences, School of Medicine, Wayne State University, 540 East Canfield, Detroit, MI 48201, USA.
Lalit P SinghDepartment of Ophthalmology, Visual and Anatomical Sciences, School of Medicine, Wayne State University, 540 East Canfield, Detroit, MI 48201, USA.
Ahmed S IbrahimDepartment of Ophthalmology, Visual and Anatomical Sciences, School of Medicine, Wayne State University, 540 East Canfield, Detroit, MI 48201, USA.ORCID 0000-0001-8480-6252
Wayne State University · USMansoura University · EG

Funding

VISION RESEARCH--COREP30EY004068 · NEI · WAYNE STATE UNIVERSITY · PI LINDA D HAZLETT · 1985 to 2026
$13.2M
Thioredoxin Interacting Protein (TXNIP) expression is critical in the development of early diabetic retinopathyR01EY023992 · NEI · WAYNE STATE UNIVERSITY · PI PUKHRAMBAM, LALIT SINGH · 2015 to 2020
$2.0M
American Heart Association American Heart Association Grant 18CDA34080403NEI NIH HHS P30 EY004068NEI NIH HHS R01 EY023992
6 · The paper itself

Abstract

Disruption of retinal pigment epithelial (RPE) barrier integrity is involved in the pathology of several blinding retinal diseases including age-related macular degeneration (AMD) and diabetic retinopathy (DR), but the underlying causes and pathophysiology are not completely well-defined. Mitochondria dysfunction has often been considered as a potential candidate implicated in such a process. In this study, we aimed to dissect the role of different mitochondrial components; specifically, those of oxidative phosphorylation (OxPhos), in maintaining the barrier functionality of RPE. Electric cell-substrate impedance sensing (ECIS) technology was used to collect multi-frequency electrical impedance data to assess in real-time the barrier formation of the RPE cells. For this purpose, the human retinal pigment epithelial cell line-ARPE-19-was used and treated with varying concentrations of specific mitochondrial inhibitors that target different steps in OxPhos: Rotenone for complex I (the largest protein complex in the electron transport chain (ETC)); oligomycin for ATP synthase; and carbonyl cyanide-p-trifluoromethoxyphenyl hydrazone (FCCP) for uncoupling ATP synthesis from the accompanying ETC. Furthermore, data were modeled using the ECIS-Zθ software to investigate in depth the effects of these inhibitors on three separate barrier parameters: cell-cell interactions (R

Indexed as

Blood-Retinal BarrierCarbonyl Cyanide p-TrifluoromethoxyphenylhydrazoneCell LineCell SurvivalDiabetic RetinopathyElectric ImpedanceElectron TransportEnzyme InhibitorsEpithelial CellsHumansMacular DegenerationMitochondriaMitochondrial Proton-Translocating ATPasesOligomycinsOxidative PhosphorylationRetinal Pigment EpitheliumCarbonyl Cyanide p-TrifluoromethoxyphenylhydrazoneEnzyme InhibitorsMitochondrial Proton-Translocating ATPasesOligomycinsRotenoneAMDARPE-19DRECISmitochondriaoxidative phosphorylationRPEuncouplers

Identifiers

PMID34360894
PMCPMC8348500
OpenAlexW3192277343

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.