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dc.contributor.authorÖztürk-Öncel, M.Ö.
dc.contributor.authorErkoc-Biradli, F.Z.
dc.contributor.authorRasier, R.
dc.contributor.authorMarcali, M.
dc.contributor.authorCaglar, E.
dc.contributor.authorGaripcan, B.
dc.date.accessioned2021-06-10T19:38:18Z
dc.date.available2021-06-10T19:38:18Z
dc.date.issued2021
dc.identifier.issn0928-4931
dc.identifier.urihttps://doi.org/10.1016/j.msec.2021.112147
dc.identifier.urihttp://hdl.handle.net/11446/4283
dc.description2-s2.0-85105450948en_US
dc.description.abstractLow proliferation capacity of corneal endothelial cells (CECs) and worldwide limitations in transplantable donor tissues reveal the critical need of a robust approach for in vitro CEC growth. However, preservation of CEC-specific phenotype with increased proliferation has been a great challenge. Here we offer a biomimetic cell substrate design, by optimizing mechanical, topographical and biochemical characteristics of materials with CEC microenvironment. We showed the surprising similarity between topographical features of white rose petals and corneal endothelium due to hexagonal cell shapes and physiologically relevant cell density (? 2000 cells/mm2). Polydimethylsiloxane (PDMS) substrates with replica of white rose petal topography and cornea-friendly Young's modulus (211.85 ± 74.9 kPa) were functionalized with two of the important corneal extracellular matrix (ECM) components, collagen IV (COL 4) and hyaluronic acid (HA). White rose petal patterned and COL 4 modified PDMS with optimized stiffness provided enhanced bovine CEC response with higher density monolayers and increased phenotypic marker expression. This biomimetic approach demonstrates a successful platform to improve in vitro cell substrate properties of PDMS for corneal applications, suggesting an alternative environment for CEC-based therapies, drug toxicity investigations, microfluidics and organ-on-chip applications. © 2021 Elsevier B.V.en_US
dc.description.sponsorship11501, 6701en_US
dc.description.sponsorshipThis study was supported by Bogazici University Research Fund by Grant Numbers 11501 and 6701 .en_US
dc.language.isoengen_US
dc.publisherElsevier Ltden_US
dc.identifier.doi10.1016/j.msec.2021.112147en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBiomimetic cell substrateen_US
dc.subjectCollagen IVen_US
dc.subjectCorneal endotheliumen_US
dc.subjectHyaluronic acid.en_US
dc.subjectPolydimethylsiloxaneen_US
dc.subjectWhite rose petalen_US
dc.titleRose petal topography mimicked poly(dimethylsiloxane) substrates for enhanced corneal endothelial cell behavioren_US
dc.typearticleen_US
dc.relation.journalMaterials Science and Engineering Cen_US
dc.department[0-Belirlenecek]en_US
dc.identifier.volume126en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.institutionauthor[0-Belirlenecek]
dc.department-tempÖztürk-Öncel, M.Ö., Institute of Biomedical Engineering, Boğaziçi University, Istanbul, Turkey; Erkoc-Biradli, F.Z., Institute of Biomedical Engineering, Boğaziçi University, Istanbul, Turkey; Rasier, R., Department of Ophthalmology, Demiroglu Bilim University, Istanbul, Turkey; Marcali, M., UNAM-National Nanotechnology Research Center, Institute of Materials Science and Nanotechnology, Bilkent University, Ankara, Turkey; Caglar, E., UNAM-National Nanotechnology Research Center, Institute of Materials Science and Nanotechnology, Bilkent University, Ankara, Turkey, Faculty of Biochemistry and Molecular Medicine, Faculty of Medicine, University of Oulu, Oulu, 90014, Finland; Garipcan, B., Institute of Biomedical Engineering, Boğaziçi University, Istanbul, Turkeyen_US


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