Evidence map›Paper›PMID 24599476›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2014

Macroglia-microglia interactions via TSPO signaling regulates microglial activation in the mouse retina.

Minhua Wang, Xu Wang, Lian Zhao, Wenxin Ma, Ignacio R Rodriguez, Robert N Fariss, Wai T Wong

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 116 papers.

0numbers the graph read from it
0cells of the map it votes in
116citing papers in PubMed
11.1field-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

116 citing papers in PubMed, 200 citations in OpenAlex.

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  7. Characteristics of TSPO expression in marmoset EAE.Journal of neuroinflammation · 2025
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56 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

7 authors at 2 institutions in 1 country.

Minhua WangUnit on Neuron-Glia Interactions in Retinal Disease, Mechanism of Retinal Diseases Section, Laboratory of Retinal Cell and Molecular Biology, and Biological Imaging Core, National Eye institute, National Institutes of Health, Bethesda, Maryland 20892.
Xu Wang
Lian Zhao
Wenxin Ma
Ignacio R Rodriguez
Robert N Fariss
Wai T Wong
National Eye Institute · USNational Institutes of Health · US

Funding

Imaging Core UnitZICEY000459 · NEI · NATIONAL EYE INSTITUTE · PI FARISS, ROBERT · 2009 to 2025
$13.1M
Dynamic Imaging of Retinal MicrogliaZIAEY000463 · NEI · NATIONAL EYE INSTITUTE · PI WONG, WAI · 2009 to 2020
$7.3M
Lipid transport, oxidation and toxicity in the retinaZIAEY000307 · NEI · NATIONAL EYE INSTITUTE · PI RODRIGUEZ, IGNACIO R · 2009 to 2014
$7.1M
Role of Microglia in the Retina in Retinal DiseasesZIAEY000541 · NEI · NATIONAL EYE INSTITUTE · PI WONG, WAI · 2014 to 2020
$5.2M
Microglial Inhibition as a Therapeutic Strategy for Subretinal HemorrhageZIAEY000505 · NEI · NATIONAL EYE INSTITUTE · PI WONG, WAI · 2011 to 2019
$1.9M
Intramural NIH HHS
6 · The paper itself

Abstract

Chronic retinal inflammation in the form of activated microglia and macrophages are implicated in the etiology of neurodegenerative diseases of the retina, including age-related macular degeneration, diabetic retinopathy, and glaucoma. However, molecular biomarkers and targeted therapies for immune cell activation in these disorders are currently lacking. To address this, we investigated the involvement and role of translocator protein (TSPO), a biomarker of microglial and astrocyte gliosis in brain degeneration, in the context of retinal inflammation. Here, we find that TSPO is acutely and specifically upregulated in retinal microglia in separate mouse models of retinal inflammation and injury. Concomitantly, its endogenous ligand, diazepam-binding inhibitor (DBI), is upregulated in the macroglia of the mouse retina such as astrocytes and Müller cells. In addition, we discover that TSPO-mediated signaling in microglia via DBI-derived ligands negatively regulates features of microglial activation, including reactive oxygen species production, TNF-α expression and secretion, and microglial proliferation. The inducibility and effects of DBI-TSPO signaling in the retina reveal a mechanism of coordinated macroglia-microglia interactions, the function of which is to limit the magnitude of inflammatory responses after their initiation, facilitating a return to baseline quiescence. Our results indicate that TSPO is a promising molecular marker for imaging inflammatory cell activation in the retina and highlight DBI-TSPO signaling as a potential target for immodulatory therapies.

Indexed as

Amino Acid SequenceAnimalsAstrocytesCell CommunicationCells, CulturedFemaleInflammationMaleMiceMice, Inbred C57BLMice, TransgenicMicrogliaMolecular Sequence DataReceptors, GABARetinaSignal TransductionBzrp protein, mouseReceptors, GABADBIgliosismicrogliaMüller cellsretinaTSPO

Identifiers

PMID24599476
PMCPMC3942591
OpenAlexW2012812017

What Socratic holds

Textmetadata
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 Socratic graph.