Evidence map›Paper›PMID 39812800›Full record

ArticleGraefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie2025

Long-term cultivation of retinal pigment epithelium cells on nanofiber scaffolds.

Julian A Zimmermann, Lucy Irlenbusch, Uwe Hansen, Marcus Himmler, Chun Zeng, Nicole Eter, Thomas Fuchsluger, Peter Heiduschka

Abstract read
In one paragraph

Article in Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Review
  2. Article
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

8 authors.

Julian A ZimmermannDepartment of Ophthalmology, University Hospital Munster, Munster, Germany.ORCID http://orcid.org/0000-0002-0007-147X
Lucy IrlenbuschDepartment of Ophthalmology, University Hospital Munster, Munster, Germany.
Uwe HansenInstitute of Musculoskeletal Medicine, University Hospital Munster, Munster, Germany.
Marcus HimmlerInstitute of Polymer Materials, Friedrich-Alexander University Erlangen-Nuremberg, Erlangen, Germany.
Chun ZengDepartment of Ophthalmology, University Hospital Munster, Munster, Germany.
Nicole EterDepartment of Ophthalmology, University Hospital Munster, Munster, Germany.
Thomas FuchslugerDepartment of Ophthalmology, University Medical Center Rostock, Rostock, Germany.
Peter HeiduschkaDepartment of Ophthalmology, University Hospital Munster, Munster, Germany. peter.heiduschka@ukmuenster.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe retinal pigment epithelium (RPE) plays an important role in the pathogenesis of age-related macular degeneration (AMD) and other retinal degenerative diseases. The introduction of healthy RPE cell cultures into the subretinal space offers a potential treatment strategy. The aim of this study was the long-term culture and characterisation of RPE cells on nanofiber scaffolds.

methodsNanofiber scaffolds consisting of polycaprolactone (PCL) and collagen were prepared by electrospinning. Porcine RPE cell cultures were maintained on PCL scaffolds, PCL-collagen scaffolds, and controls at the bottom of 24-well plates. Cell culture analysis was performed by immunohistochemistry, while the release of inflammatory cytokines IL-6, IL-8, TNF-α, and PDGF-β was measured by ELISA and multiplex assays. Ultrastructural features were examined by transmission electron microscopy.

resultsThe observation period averaged 42.7 weeks for controls, 38.7 weeks for PCL scaffold cultures, and 36.1 weeks for PCL-collagen scaffold cultures, with cell number and morphology remaining stable. TNF-α levels in the supernatants were minimal, IL-6 levels were consistently low, and IL-8 levels decreased from initially high to lower levels over time.

conclusionRPE cells were stably cultured on nanofiber scaffolds for extended periods of time. The long-term physiological properties of RPE cells, including phagocytic ability and visual cycle enzyme activity, need to be further investigated before clinical application. In addition, controlling the expression of inflammatory mediators is a major challenge. Despite these hurdles, overcoming them is critical given the increasing prevalence of retinal degenerative diseases.

Indexed as

Cell Culture TechniquesNanofibersRetinal Pigment EpitheliumTissue EngineeringTissue ScaffoldsAnimalsCells, CulturedCytokinesEnzyme-Linked Immunosorbent AssayImmunohistochemistryMicroscopy, Electron, TransmissionPolyestersSwineTime FactorsCytokinespolycaprolactonePolyestersCell cultureCell replacementMacular degenerationNanofiber scaffoldsPorcine retinal pigment epithelium

Identifiers

PMID39812800
PMCPMC12149269

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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.