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A Novel 3D Cultured Model for Studying Early Changes in Age‐Related Macular Degeneration
Author(s) -
Shokoohmand Ali,
Jeon June E.,
Theodoropoulos Christina,
Baldwin Jeremy G.,
Hutmacher Dietmar W.,
Feigl Beatrix
Publication year - 2017
Publication title -
macromolecular bioscience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.924
H-Index - 105
eISSN - 1616-5195
pISSN - 1616-5187
DOI - 10.1002/mabi.201700221
Subject(s) - macular degeneration , retinal pigment epithelium , gelatin , pathogenesis , retinal , microbiology and biotechnology , chemistry , choroidal neovascularization , in vitro , pathology , biology , medicine , ophthalmology , biochemistry
Various in vitro culture systems have been used to investigate the pathogenesis of age‐related macular degeneration (AMD). However, many still rely on oversimplified monolayer culture models. AMD is a complex disease, associated with the pathological changes to multiple structural components such as the Bruch's membrane, retinal pigment epithelium (RPE), and choroidal endothelial cells. This study aims to construct a novel 3D coculture model using the polycaprolactone (PCL)‐gelatin electrospun scaffold, with human RPE cells (hRPE) and primate choroidal cells (RF‐6A). Results from this study show that PCL‐gelatin scaffolds have a highly porous ultrastructure that supports the attachment, proliferation, differentiation, and migration of the hRPEs and choroidal endothelial cells. It is also demonstrated that the PCL‐gelatin 3D coculture model may be useful in exploring the molecular interplay between the hPRE and the choroidal endothelial cells, and their effects on growth factor modulation, which may be important in the pathogenesis of AMD.