Evidence map›Paper›PMID 30308581›Full record

ArticleCornea2019

Descemet's Membrane Biomimetic Microtopography Differentiates Human Mesenchymal Stem Cells Into Corneal Endothelial-Like Cells.

Angela Gutermuth, Jessika Maassen, Emely Harnisch, Daniel Kuhlen, Alexis Sauer-Budge, Claudia Skazik-Voogt, Katrin Engelmann

Open access · hybridAbstract read
In one paragraph

Article in Cornea, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

25 citing papers in PubMed, 45 citations in OpenAlex.

  1. Review
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  3. Advances in corneal transplantation.Eye (London, England) · 2025
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  18. Unraveling the mechanobiology of cornea: From bench side to the clinic.Frontiers in bioengineering and biotechnology · 2022
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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 3 institutions in 2 countries.

Angela GutermuthDepartment for Applied Cell Biology, Fraunhofer Institute for Production Technology, Aachen, Germany.
Jessika MaassenDepartment for Applied Cell Biology, Fraunhofer Institute for Production Technology, Aachen, Germany.
Emely HarnischDepartment for Applied Cell Biology, Fraunhofer Institute for Production Technology, Aachen, Germany.
Daniel KuhlenDepartment for Applied Cell Biology, Fraunhofer Institute for Production Technology, Aachen, Germany.
Alexis Sauer-BudgeExponent, Department for Polymer Science & Materials Chemistry, Natick, MA.
Claudia Skazik-VoogtDepartment for Applied Cell Biology, Fraunhofer Institute for Production Technology, Aachen, Germany.
Katrin EngelmannMedical Center for Ophthalmology, Chemnitz, Germany.
Fraunhofer Institute for Production Technology IPT · DEExponent (United States) · USKlinikum Chemnitz · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeLoss of corneal endothelial cells (CECs) bears disastrous consequences for the patient, including corneal clouding and blindness. Corneal transplantation is currently the only therapy for severe corneal disorders. However, the worldwide shortages of corneal donor material generate a strong demand for personalized stem cell-based alternative therapies. Because human mesenchymal stem cells are known to be sensitive to their mechanical environments, we investigated the mechanotransductive potential of Descemet membrane-like microtopography (DLT) to differentiate human mesenchymal stem cells into CEC-like cells.

methodsMaster molds with inverted DLT were produced by 2-photon lithography (2-PL). To measure the mechanotransductive potential of DLT, mesenchymal stem cells were cultivated on silicone or collagen imprints with DLT. Changes in morphology were imaged, and changes in gene expression of CEC typical genes such as zonula occludens (ZO-1), sodium/potassium (Na/K)-ATPase, paired-like homeodomain 2 (PITX2), and collagen 8 (COL-8) were measured with real-time polymerase chain reaction. At least immunofluorescence analysis has been conducted to confirm gene data on the protein level.

resultsAdhesion of MSCs to DLT molded in silicone and particularly in collagen initiates polygonal morphology and monolayer formation and enhances not only transcription of CEC typical genes such as ZO-1, Na/K-ATPase, PITX2, and COL-8 but also expression of the corresponding proteins.

conclusionsArtificial reproduction of Descemet membrane with respect to topography and similar stiffness offers a potential innovative way to bioengineer a functional CEC monolayer from autologous stem cells.

Indexed as

Corneal TransplantationAnimalsBiomimeticsCell CountCells, CulturedCorneal DiseasesDescemet MembraneEndothelium, CornealFlow CytometryHumansMaleMesenchymal Stem CellsMicroscopy, Electron, ScanningPhotomicrographyRabbits

Identifiers

PMID30308581
PMCPMC6282677
OpenAlexW2897463261

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.