Evidence map›Paper›PMID 30893912›Full record

ArticleInternational journal of molecular sciences2019

Deletion of TSPO Resulted in Change of Metabolomic Profile in Retinal Pigment Epithelial Cells.

Abdulwahab Alamri, Lincoln Biswas, David G Watson, Xinhua Shu

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 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.4field-weighted citation impact, top 13% 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

9 citing papers in PubMed, 18 citations in OpenAlex.

  1. The roles of glycerophospholipids in the aging retina and age-related macular degeneration.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2026
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  9. Commentary:Frontiers in endocrinology · 2020
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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.

Abdulwahab AlamriDepartment of Pharmacology, College of Pharmacy Sciences, University of Hail, Hail 55476, Saudi Arabia. ph.whab@gmail.com.
Lincoln BiswasDepartment of Biological and Biomedical Sciences, Glasgow Caledonian University, Glasgow G4 0BA, UK. Lincoln.Biswas@gcu.ac.uk.ORCID 0000-0002-2288-341X
David G WatsonStrathclyde Institute of Pharmacy and Biomedical Science, University of Strathclyde, Glasgow G4 0RE, UK. d.g.watson@strath.ac.uk.ORCID 0000-0003-1094-7604
Xinhua ShuDepartment of Biological and Biomedical Sciences, Glasgow Caledonian University, Glasgow G4 0BA, UK. Xinhua.Shu@gcu.ac.uk.ORCID 0000-0003-3760-3019
Glasgow Caledonian University · GBUniversity of Strathclyde · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Age-related macular degeneration is the main cause of vision loss in the aged population worldwide. Drusen, extracellular lesions formed underneath the retinal pigment epithelial (RPE) cells, are a clinical feature of AMD and associated with AMD progression. RPE cells support photoreceptor function by providing nutrition, phagocytosing outer segments and removing metabolic waste. Dysfunction and death of RPE cells are early features of AMD. The translocator protein, TSPO, plays an important role in RPE cholesterol efflux and loss of TSPO results in increased intracellular lipid accumulation and reactive oxygen species (ROS) production. This study aimed to investigate the impact of TSPO knockout on RPE cellular metabolism by identifying the metabolic differences between wildtype and knockout RPE cells, with or without treatment with oxidized low density lipoprotein (oxLDL). Using liquid chromatography mass spectrometry (LC/MS), we differentiated several metabolic pathways among wildtype and knockout cells. Lipids amongst other intracellular metabolites were the most influenced by loss of TSPO and/or oxLDL treatment. Glucose, amino acid and nucleotide metabolism was also affected. TSPO deletion led to up-regulation of fatty acids and glycerophospholipids, which in turn possibly affected the cell membrane fluidity and stability. Higher levels of glutathione disulphide (GSSG) were found in

Indexed as

Gene DeletionMetabolomicsCell LineDiscriminant AnalysisEpithelial CellsGlucoseGlutathione DisulfideHumansLipid MetabolismLipoproteins, LDLMetabolomeNucleotidesOxidative StressPrincipal Component AnalysisReceptors, GABARetinal Pigment EpitheliumGlucoseGlutathione DisulfideLipoproteins, LDLNucleotidesoxidized low density lipoproteinReceptors, GABATSPO protein, humanage related macular degenerationmetabolitesretinal pigment epithelial cellsTSPO

Identifiers

PMID30893912
PMCPMC6470938
OpenAlexW2924793698

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.