Performing subretinal injections in rodents to deliver retinal pigment epithelium cells in suspension

• Published in: Journal of visualized experiments no. 95; p. 52247
• Main Authors: Westenskow, Peter D, Kurihara, Toshihide, Bravo, Stephen, Feitelberg, Daniel, Sedillo, Zack A, Aguilar, Edith, Friedlander, Martin
• Format: Journal Article
• Language: English
• Published: United States MyJove Corporation 23.01.2015
• Subjects: Animals; Disease Models, Animal; Injections - methods; Macular Degeneration - therapy; Medicine; Mice; Photoreceptor Cells; Pluripotent Stem Cells; Rats; Retinal Pigment Epithelium - cytology; Retinal Pigment Epithelium - transplantation; Tomography, Optical Coherence - methods
• ISSN: 1940-087X; 1940-087X
• DOI: 10.3791/52247

The conversion of light into electrical impulses occurs in the outer retina and is accomplished largely by rod and cone photoreceptors and retinal pigment epithelium (RPE) cells. RPE provide critical support for photoreceptors and death or dysfunction of RPE cells is characteristic of age-related macular degeneration (AMD), the leading cause of permanent vision loss in people age 55 and older. While no cure for AMD has been identified, implantation of healthy RPE in diseased eyes may prove to be an effective treatment, and large numbers of RPE cells can be readily generated from pluripotent stem cells. Several interesting questions regarding the safety and efficacy of RPE cell delivery can still be examined in animal models, and well-accepted protocols used to inject RPE have been developed. The technique described here has been used by multiple groups in various studies and involves first creating a hole in the eye with a sharp needle. Then a syringe with a blunt needle loaded with cells is inserted through the hole and passed through the vitreous until it gently touches the RPE. Using this injection method, which is relatively simple and requires minimal equipment, we achieve consistent and efficient integration of stem cell-derived RPE cells in between the host RPE that prevents significant amount of photoreceptor degeneration in animal models. While not part of the actual protocol, we also describe how to determine the extent of the trauma induced by the injection, and how to verify that the cells were injected into the subretinal space using in vivo imaging modalities. Finally, the use of this protocol is not limited to RPE cells; it may be used to inject any compound or cell into the subretinal space.