Sign In

A subscription to JoVE is required to view this content. Sign in or start your free trial.

In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Disclosures
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

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.

Abstract

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.

Introduction

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 ....

Protocol

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 ....

Representative Results

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.......

Discussion

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.......

Disclosures

None.

Acknowledgements

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)....

Materials

NameCompanyCatalog NumberComments
6 Micro-well glass bottom plate with 14 mm micro-well #1 cover glassCellvisP06-14-1-N
Antibiotic-Antimycotic (100x)Gibco15240062
Biosafety Cabinet
Calcium Chloride, Dried, Powder, 97%Alfa AesarL13191.30
Cell StrainerFisher Scientific 22-363-548one per eye
Centrifuge
Centrifuge Tubes, 15 mLFisher Scientific 05-539-12
Cooler, 8 LIgloo32529
Corning Transwell Multiple Well Plate with Permeable Polyester Membrane InsertsFisher Scientific 07-200-154Culture inserts
Cut Resistant GloveDowellife712971375857
Cytiva HyClone Dulbecco's Phosphate Buffered Saline, SolutionFisher Scientific SH3026401for ICC dilutions only 
Deionized Water
DMEM, 1x with 4.5 g/L glucose, L-glutamine & sodium pyruvateCorning10-013-CV
DNase I from Bovine PancreasSigma AldrichDN25
DPBS/Modified - calcium - magnesiumCytivaSH3002B.02stored at 4 °C
ELISA kit, Q-Plex Human Angiogenesis (9-Plex) Quansys Biosciences, Logan, UT
ENDOHM 6 TEER deviceWorld Precision Instruments
Fetal Bovine Serum (FBS)Avantor232B20
Fisher BioReagents Bovine Serum Albumin (BSA) DNase- and Protease-free PowderFisher Scientific BP9706100
Flashlight
Formaldehyde, ACS Grade, 36.5% (w/w) to 38.0% (w/w), LabChemFisher Scientific LC146501
Gauze SpongesFisher Scientific 22-415-504One per eye
Goat anti-Mouse IgG (H+L) Highly Cross-Adsorbed Secondary Antibody, Alexa Fluor Plus 647, InvitrogenThermo ScientificA32728RPE65 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-PalmerEW-10818-05
Iris Scissors, 11 cm, Straight, Tungsten CarbideFisher Scientific 50-822-379
LSM-710 Confocal MicroscopeZeiss
Petri Dish, 100 mm x 20 mm Corning430167one per 2-3 eyes and one for dissection surface/waste 
Povidone-Iondine Solution, 10%Equate49035-050-34
RPE65 Monoclonal Antibody (401.8B11.3D9), InvitrogenThermo ScientificMA116578RPE65 primary antibody
Scalpel Blades Size 10Fisher Scientific 22-079-683
Scalpel Handles Style 3Fisher Scientific 50-118-4164
Surgical Drape, 18 x 26"Fisher Scientific 50-209-1792
Tissue Culture Incubator37 °C, 5% CO2, 95% Humidity
Tissue Culture Plates, 6 WellsVWR10062-892One for eye wash and one for seeding 
Tri-Cornered Polypropylene Beaker, 1000 mLFisher Scientific 14-955-111F
Triton X-100Sigma AldrichT8787
Trypsin 0.25%, 2.21 mM EDTA in HBSS; w/o Ca, Mg, Sodium BicarbonateCorning25053Cl
Tweezers Style 20AFisher Scientific 17-467-231
Tweezers Style 2AFisher Scientific 50-238-47for removing neural retina
Tweezers Style 5-SA-PIFisher Scientific 17-467-168
Vacuum Aspiration System
Water Bath, 37 °C
ZO-1 Monoclonal Antibody (ZO1-1A12), FITC, InvitrogenFisher Scientific 33-911-1ZO-1 conjugated primary antibody

References

  1. Booij, J. C., Baas, D. C., Beisekeeva, J., Gorgels, T. G. M. F., Bergen, A. A. B. The dynamic nature of Bruch's membrane. Progress in Retinal and Eye Research. 29 (1), 1-18 (2010).
  2. Caceres, P. S., Rodriguez-Boulan, E. Retinal pigment epithelium p....

Reprints and Permissions

Request permission to reuse the text or figures of this JoVE article

Request Permission

Explore More Articles

Primary Porcine Retinal Pigment Epithelial CellsIn Vitro ModelingRetinal PathologiesRPE DegenerationAge related Macular Degeneration AMDInduced Pluripotent Stem Cells iPSCsARPE 19 Cell LineTissue CultureCost effective RPE Source

This article has been published

Video Coming Soon

JoVE Logo

Privacy

Terms of Use

Policies

Research

Education

ABOUT JoVE

Copyright © 2025 MyJoVE Corporation. All rights reserved