Utilizing Recombinant Spider Silk Proteins To Develop a Synthetic Bruch’s Membrane for Modeling the Retinal Pigment Epithelium
Document Type
Article
Journal/Book Title
ACS Biomaterials Science & Engineering
Publication Date
7-2-2019
Award Number
NIH 1R15EY028732-01A1
Funder
NIH
Publisher
American Chemical Society
Volume
5
Issue
8
Abstract
Spider silks are intriguing biomaterials that have a high potential as innovative biomedical processes and devices. The intent of this study was to evaluate the capacity of recombinant spider silk proteins (rSSps) as a synthetic Bruch’s membrane. Nonporous silk membranes were prepared with comparable thicknesses (<10 >μm) to that of native Bruch’s membrane. Biomechanical characterization was performed prior to seeding cells. The ability of RPE cells (ARPE-19) to attach and grow on the membranes was then evaluated with bright-field and electron microscopy, intracellular DNA quantification, and immunocytochemical staining (ZO-1 and F-actin). Controls were cultured on permeable Transwell support membranes and characterized with the same methods. A size-dependent permeability assay, using FITC–dextran, was used to determine cell-membrane barrier function. Compared to Transwell controls, RPE cells cultured on rSSps membranes developed more native-like “cobblestone” morphologies, exhibited higher intracellular DNA content, and expressed key organizational proteins more consistently. Comparisons of the membranes to native structures revealed that the silk membranes exhibited equivalent thicknesses, biomechanical properties, and barrier functions. These findings support the use of recombinant spider silk proteins to model Bruch’s membrane and develop more biomimetic retinal models.
First Page
4023
Last Page
4036
Recommended Citation
Harris, Thomas I., et al. “Utilizing Recombinant Spider Silk Proteins To Develop a Synthetic Bruch’s Membrane for Modeling the Retinal Pigment Epithelium.” ACS Biomaterials Science & Engineering, vol. 5, no. 8, American Chemical Society, Aug. 2019, pp. 4023–36, doi:10.1021/acsbiomaterials.9b00183.