Evidence map›Paper›PMID 32859013›Full record

ArticleAntioxidants (Basel, Switzerland)2020

Properdin Modulates Complement Component Production in Stressed Human Primary Retinal Pigment Epithelium Cells.

Nicole Schäfer, Hannah N Wolf, Anne Enzbrenner, Juliane Schikora, Maria Reichenthaler, Volker Enzmann, Diana Pauly

Open access · goldAbstract read
In one paragraph

Article in Antioxidants (Basel, Switzerland), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

11 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Complement C3 Activation in the Human Retinal Pigment Epithelium.Investigative ophthalmology & visual science · 2025
    Article
  4. Article
  5. Article
  6. 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

7 authors at 2 institutions in 2 countries.

Nicole SchäferExperimental Ophthalmology, Eye clinic, University Hospital Regensburg, 93053 Regensburg, Germany.
Hannah N WolfExperimental Ophthalmology, Eye clinic, University Hospital Regensburg, 93053 Regensburg, Germany.
Anne EnzbrennerExperimental Ophthalmology, Eye clinic, University Hospital Regensburg, 93053 Regensburg, Germany.
Juliane SchikoraExperimental Ophthalmology, Eye clinic, University Hospital Regensburg, 93053 Regensburg, Germany.
Maria ReichenthalerExperimental Ophthalmology, Eye clinic, University Hospital Regensburg, 93053 Regensburg, Germany.
Volker EnzmannDepartment of Ophthalmology, University Hospital of Bern and Department of Biomedical Research, University of Bern, 3010 Bern, Switzerland.ORCID 0000-0003-4384-4855
Diana PaulyExperimental Ophthalmology, Eye clinic, University Hospital Regensburg, 93053 Regensburg, Germany.ORCID 0000-0002-1563-1601
University Hospital Regensburg · DEUniversity of Bern · CH

Funding

Velux Stiftung 1103
6 · The paper itself

Abstract

The retinal pigment epithelium (RPE) maintains visual function and preserves structural integrity of the retina. Chronic dysfunction of the RPE is associated with retinal degeneration, including age-related macular degeneration (AMD). The AMD pathogenesis includes both increased oxidative stress and complement dysregulation. Physiological sources of oxidative stress in the retina are well known, while complement sources and regulation are still under debate. Using human primary RPE (hpRPE) cells, we have established a model to investigate complement component expression on transcript and protein level in AMD-risk and non-risk hpRPE cells. We evaluated the effect of properdin, a complement stabilizer, on the hpRPE cell-dependent complement profile exposed to oxidative stress. hpRPE cells expressed complement components, receptors and regulators. Complement proteins were also stored and secreted by hpRPE cells. We associated AMD-risk single nucleotide polymorphisms with an increased secretion of complement factors D (CFD) and I (CFI). Furthermore, we detected hpRPE cell-associated complement activation products (C3a, C5a) independent of any extracellularly added complement system. Exogenous properdin increased the mRNA expression of

Indexed as

AMD-risk genotypecell-associatedcomplement systemhumaninflammasomeintracellularoxidative stressproperdinretinal pigment epithelium

Identifiers

PMID32859013
PMCPMC7555107
OpenAlexW3080354946

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.