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ABSTRACT: Background
In inherited retinal disorders such as retinitis pigmentosa (RP), rod photoreceptor-specific mutations cause primary rod degeneration that is followed by secondary cone death and loss of high-acuity vision. Mechanistic studies of retinal degeneration are challenging because of retinal heterogeneity. Moreover, the detection of early cone responses to rod death is especially difficult due to the paucity of cones in the retina. To resolve heterogeneity in the degenerating retina and investigate events in both types of photoreceptors during primary rod degeneration, we utilized droplet-based single-cell RNA sequencing in an RP mouse model, rd10.Results
Using trajectory analysis, we defined two consecutive phases of rod degeneration at P21, characterized by the early
SUBMITTER: Karademir D
PROVIDER: S-EPMC9006580 | biostudies-literature | 2022 Apr
REPOSITORIES: biostudies-literature