PEDF and Derived Peptides Prevent Apoptosis and Promote Differentiation of Retinal Photoreceptors

Pigment epithelium-derived factor (PEDF) is a cytoprotective protein for the retina. We hypothesize that this protein acts on neuronal survival and differentiation of photoreceptor cells in culture. The purpose of the present study was to evaluate the neurotrophic effects of PEDF and its fragments in an in vitro model of cultured primary retinal neurons that die spontaneously in the absence of trophic factors. Results show that PEDF protected photoreceptor precursors from apoptosis, preserved mitochondrial function and promoted polarization of opsin enhancing their developmental process, as well as induced neurite outgrowth in amacrine neurons. These effects were abolished by an inhibitor of the PEDF receptor or receptor-derived peptides that block ligand/receptor interactions. While all the activities were specifically conferred by short peptide fragments (17 amino acid residues) derived from the PEDF neurotrophic domain, no effects were triggered by peptides from the PEDF antiangiogenic region. The observed effects on retinal neurons imply a specific activation of the PEDF receptor by a small neurotrophic region of PEDF. Our findings support the neurotrophic PEDF peptides as neuronal guardians for the retina, highlighting their potential as promoters of retinal differentiation, and inhibitors of retina cell death and its blinding consequences. ### Competing Interest Statement The authors have declared no competing interest. * DIV : Days In Vitro DAPI : 4′,6-diamidino-2-phenylindole DHA : Docosahexaenoic Acid FSC : Forward-Scatter PEDF : Pigmented epithelium-derived factor PEDF-R : PEDF Receptor PI : Propidium Iodide PN : Postnatal PHR : Photoreceptor Pnpla2 : Patatin-like phospholipase-2 SSC : Side-Scatter