Isolation, culture, and cryosectioning of primary porcine retinal pigment epithelium on transwell cell culture inserts.

Erika M S Hood, Christine A Curcio, Daniel Lipinski
Author Information
  1. Erika M S Hood: Cell Biology, Neurobiology, and Anatomy, Medical College of Wisconsin, Milwaukee, WI, USA; Ophthalmology and Visual Sciences, Medical College of Wisconsin, Milwaukee, WI, USA. Electronic address: eshaw@mcw.edu.
  2. Christine A Curcio: Department of Ophthalmology and Visual Sciences, Heersink School of Medicine, University of Alabama at Birmingham, Birmingham, AL, USA.
  3. Daniel Lipinski: Cell Biology, Neurobiology, and Anatomy, Medical College of Wisconsin, Milwaukee, WI, USA; Ophthalmology and Visual Sciences, Medical College of Wisconsin, Milwaukee, WI, USA. Electronic address: dlipinski@mcw.edu.

Abstract

Primary culture and long-term maintenance of primary retinal pigment epithelium (RPE) is a useful model system for the study of ocular pathologies such as age-related macular degeneration. Here, we detail the steps for the isolation and long-term culture of primary porcine RPE. We also describe steps for cryoprotecting, cryosectioning, and interrogating with immunofluorescence and histochemistry RPE cells grown on transwell membranes. These techniques can be used in histological studies to detect sub-RPE deposits. For complete details on the use and execution of this protocol, please refer to Pilgrim et al., (2017).

Keywords

Grants

  1. R01 EY027767/NEI NIH HHS
  2. C06 RR016511/NCRR NIH HHS
  3. T32 GM080202/NIGMS NIH HHS
  4. T32 EY014537/NEI NIH HHS
  5. R01 EY032478/NEI NIH HHS

MeSH Term

Swine
Animals
Retinal Pigment Epithelium
Macular Degeneration
Cell Culture Techniques
Models, Biological
Cryoultramicrotomy

Word Cloud

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