Evidence map›Paper›PMID 42774045›Full record

ArticleMolecular vision2026

Toll-like receptor 9 in retinal pigment epithelial cells: Expression, function and the role of TGF-β1.

Elisabeth Esser, Heidrun Kuhrt, Focke Ziemssen, Margrit Hollborn

Abstract read
In one paragraph

Article in Molecular vision, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Elisabeth EsserDepartment of Ophthalmology and Eye Hospital, University of Leipzig, Leipzig, Germany.
Heidrun KuhrtInstitute of Anatomy, University of Leipzig, Germany.
Focke ZiemssenDepartment of Ophthalmology and Eye Hospital, University of Leipzig, Leipzig, Germany.
Margrit HollbornDepartment of Ophthalmology and Eye Hospital, University of Leipzig, Leipzig, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Inflammatory processes in the aged retina may be exacerbated by systemic infection with viruses and bacteria, potentially aggravating age-related macular degeneration (AMD). Toll-like receptors (TLR) are key mediators in detecting pathogen-associated molecular patterns (PAMPs) and host-derived damage-associated molecular patterns (DAMPs). This study aimed to investigate Methods: TLR gene expression was assessed using semiquantitative qPCR, while protein expression was evaluated through western blotting, immunocytochemistry, and ELISA. Hypoxic conditions were simulated using CoCl Results: Among the Conclusions: TLR9 activation under hypoxic conditions initiates pro-inflammatory pathways in RPE cells. In the aging retina, viral and bacterial infections and/or DAMPs may further amplify these responses, worsening retinal degeneration. TGF-β1 may exert protective, anti-inflammatory effects by downregulating TLR9 expression.

Indexed as

Epithelial CellsRetinal Pigment EpitheliumToll-Like Receptor 9Transforming Growth Factor beta1ApoptosisCell HypoxiaCell LineCell ProliferationCell SurvivalCellular SenescenceCobaltGene Expression RegulationHumansRNA, MessengerSignal TransductionToll-Like Receptor AgonistsCobaltcobaltous chlorideRNA, MessengerTLR9 protein, humanToll-Like Receptor 9Toll-Like Receptor AgonistsTransforming Growth Factor beta1

Identifiers

PMID42774045
PMCPMC13585427

What OpenQuestion holds

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Registered trials

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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.