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This protocol outlines the procedure for obtaining and culturing primary retinal pigment epithelial (RPE) cells from locally sourced porcine eyes. These cells serve as a high-quality alternative to stem cells and are suitable for in vitro retinal research.
The retinal pigment epithelium (RPE) is a crucial monolayer in the outer retina responsible for supporting photoreceptors. RPE degeneration commonly occurs in diseases marked by progressive vision loss, such as age-related macular degeneration (AMD). Research on AMD often relies on human donor eyes or induced pluripotent stem cells (iPSCs) to represent the RPE. However, these RPE sources require extended differentiation periods and substantial expertise for culturing. Additionally, some research institutions, particularly those in rural areas, lack easy access to donor eyes. While a commercially available immortalized RPE cell line (ARPE-19) exists, it lacks essential in vivo RPE features and is not widely accepted in many ophthalmology research publications. There is a pressing need to obtain representative primary RPE cells from a more readily available and cost-effective source. This protocol elucidates the isolation and subculture of primary RPE cells obtained post-mortem from porcine eyes, which can be sourced locally from commercial or academic suppliers. This protocol necessitates common materials typically found in tissue culture labs. The result is a primary, differentiated, and cost-effective alternative to iPSCs, human donor eyes, and ARPE-19 cells.
The retinal pigment epithelium (RPE) is a monolayer located in the outer retina between Bruch's membrane and the photoreceptors1. RPE cells form tight junctions with proteins such as zonula occludens-1 (ZO-1) and possess a distinctive phenotype characterized by pigmentation and hexagonal morphology2,3. These cells contribute to the blood-retinal barrier, thereby supporting photoreceptor health and maintaining retinal homeostasis4,5. Additionally, RPE cells play a critical role in vision by absorbing light and recycling ....
The eyes used in this procedure are obtained post-mortem from a local, USDA-inspected butcher shop, and no work is performed using live animals. After the animals have been sacrificed, approximately 2 h pass before the eyes are enucleated. As tissue decay may begin to occur, it is important to keep the eyes cool during transport to prevent further decay. In this procedure, the eyes are immediately placed into a refrigerator after enucleation. Subsequently, the bag of eyes is positioned inside a 1000 mL polypropylene beaker and surrounded by ice within an 8 L cooler. It is important not to place the eyes directly on the ice. Once the eyes arrive at the laboratory, the ....
Using this procedure, primary RPE cells were successfully isolated from porcine eyes. Figure 1A shows RPE cells 3 days post isolation with characteristic pigmentation. After 1 week of growth, cells were fully confluent and formed a healthy monolayer (Figure 1B). Cells were then transferred to cell culture inserts where they maintained their pigmentation and morphology (Figure 1C), further supporting the efficacy of the isolation pro.......
This protocol describes how to isolate RPE cells from porcine eyes. Pigmentation and cobblestone morphology are seen within 7 days of isolation (Figure 1B). Furthermore, TEER data indicate tight junction formation22 and a healthy monolayer (Figure 5). These results show that RPE cells isolated with this method are similar to human RPE and can be beneficial in retinal cell culture models.
The eyes used in this m.......
None.
The authors would like to thank Farhad Farjood for help with porcine RPE cell culture and isolation and Thomas Harris for help with SEM. The authors acknowledge the support from the Microscopy Core Facility at Utah State University for the SEM analysis. The facility maintains a scanning electron microscope acquired through a National Science Foundation Major Research Instrumentation Grant (CMMI-1337932). Funding for this study was provided by a National Institutes of Health through Grant 1R15EY028732 (Vargis) and a BrightFocus Foundation Grant M2019109 (Vargis). Additional funding was provided by an Undergraduate Research and Creative Opportunities Grant (Weatherston)....
Name | Company | Catalog Number | Comments |
6 Micro-well glass bottom plate with 14 mm micro-well #1 cover glass | Cellvis | P06-14-1-N | |
Antibiotic-Antimycotic (100x) | Gibco | 15240062 | |
Biosafety Cabinet | |||
Calcium Chloride, Dried, Powder, 97% | Alfa Aesar | L13191.30 | |
Cell Strainer | Fisher Scientific | 22-363-548 | one per eye |
Centrifuge | |||
Centrifuge Tubes, 15 mL | Fisher Scientific | 05-539-12 | |
Cooler, 8 L | Igloo | 32529 | |
Corning Transwell Multiple Well Plate with Permeable Polyester Membrane Inserts | Fisher Scientific | 07-200-154 | Culture inserts |
Cut Resistant Glove | Dowellife | 712971375857 | |
Cytiva HyClone Dulbecco's Phosphate Buffered Saline, Solution | Fisher Scientific | SH3026401 | for ICC dilutions only |
Deionized Water | |||
DMEM, 1x with 4.5 g/L glucose, L-glutamine & sodium pyruvate | Corning | 10-013-CV | |
DNase I from Bovine Pancreas | Sigma Aldrich | DN25 | |
DPBS/Modified - calcium - magnesium | Cytiva | SH3002B.02 | stored at 4 °C |
ELISA kit, Q-Plex Human Angiogenesis (9-Plex) | Quansys Biosciences, Logan, UT | ||
ENDOHM 6 TEER device | World Precision Instruments | ||
Fetal Bovine Serum (FBS) | Avantor | 232B20 | |
Fisher BioReagents Bovine Serum Albumin (BSA) DNase- and Protease-free Powder | Fisher Scientific | BP9706100 | |
Flashlight | |||
Formaldehyde, ACS Grade, 36.5% (w/w) to 38.0% (w/w), LabChem | Fisher Scientific | LC146501 | |
Gauze Sponges | Fisher Scientific | 22-415-504 | One per eye |
Goat anti-Mouse IgG (H+L) Highly Cross-Adsorbed Secondary Antibody, Alexa Fluor Plus 647, Invitrogen | Thermo Scientific | A32728 | RPE65 secondary antibody |
Ice | Crushed prefered | ||
Inverted Phase Contrast Microscope | |||
Invitrogen NucBlue Live ReadyProbes Reagent (Hoechst 33342) | Fisher Scientific | R37605 | |
Iris Fine Tip Scissors, Standard Grade, Curved, 4.5" | Cole-Palmer | EW-10818-05 | |
Iris Scissors, 11 cm, Straight, Tungsten Carbide | Fisher Scientific | 50-822-379 | |
LSM-710 Confocal Microscope | Zeiss | ||
Petri Dish, 100 mm x 20 mm | Corning | 430167 | one per 2-3 eyes and one for dissection surface/waste |
Povidone-Iondine Solution, 10% | Equate | 49035-050-34 | |
RPE65 Monoclonal Antibody (401.8B11.3D9), Invitrogen | Thermo Scientific | MA116578 | RPE65 primary antibody |
Scalpel Blades Size 10 | Fisher Scientific | 22-079-683 | |
Scalpel Handles Style 3 | Fisher Scientific | 50-118-4164 | |
Surgical Drape, 18 x 26" | Fisher Scientific | 50-209-1792 | |
Tissue Culture Incubator | 37 °C, 5% CO2, 95% Humidity | ||
Tissue Culture Plates, 6 Wells | VWR | 10062-892 | One for eye wash and one for seeding |
Tri-Cornered Polypropylene Beaker, 1000 mL | Fisher Scientific | 14-955-111F | |
Triton X-100 | Sigma Aldrich | T8787 | |
Trypsin 0.25%, 2.21 mM EDTA in HBSS; w/o Ca, Mg, Sodium Bicarbonate | Corning | 25053Cl | |
Tweezers Style 20A | Fisher Scientific | 17-467-231 | |
Tweezers Style 2A | Fisher Scientific | 50-238-47 | for removing neural retina |
Tweezers Style 5-SA-PI | Fisher Scientific | 17-467-168 | |
Vacuum Aspiration System | |||
Water Bath, 37 °C | |||
ZO-1 Monoclonal Antibody (ZO1-1A12), FITC, Invitrogen | Fisher Scientific | 33-911-1 | ZO-1 conjugated primary antibody |
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