Abstract
Retinal ganglion cells (RGCs) transmit visual information from the eye to the brain, but do not regenerate after damage. Understanding RGC development aids regeneration. In this study, we investigated the regulatory network of two transforming growth factor β (TGFβ) superfamily proteins, growth and differentiation factors (GDF) 11 and 15, which exhibit opposing effects on RGC differentiation. To explore their roles in retinal development, we studied GDF11, GDF15, and Tgfβr2 using cre-driven conditional knockout mice. Gdf11 deletion promoted RGC differentiation, an effect lost when Gdf15 was also knocked out, suggesting that GDF15 counteracts the differentiation-promoting effects of GDF11. Tgfβr2 knockout increased RGCs but reduced photoreceptors, indicating a broader influence on retinal cell fate. Transcriptomic analysis revealed altered RGC subtype markers and genes involved in axon formation and guidance. These findings highlight a GDF-TGFβ regulatory network in RGC specification and provide insights into potential therapeutic targets for retinal regeneration.
Keywords:
Cell biology; Developmental biology; Transcriptomics.