Ontology highlight
ABSTRACT: Purpose
One of the leading causes of irreversible blindness worldwide, age-related macular degeneration (AMD) is a progressive disorder leading to retinal degeneration. While several treatment options exist for the exudative form of AMD, there are currently no FDA-approved treatments for the more common nonexudative (atrophic) form. Mounting evidence suggests that mitochondrial damage and retinal pigment epithelium (RPE) cell death are linked to the pathogenesis of AMD. Human retinal progenitor cells (hRPCs) have been studied as a potential restorative therapy for degenerative conditions of the retina; however, the effects of hRPC treatment on retinal cell survival in AMD have not been elucidated.Methods
In this study, we used a cell coculture system consisting of hRPCs and
SUBMITTER: Yu JJ
PROVIDER: S-EPMC7886532 | biostudies-literature | 2021
REPOSITORIES: biostudies-literature