Exosomes derived from RPE cells under oxidative stress mediate inflammation and apoptosis of normal RPE cells through Apaf1/caspase‐9 axis

AbstractThis study aims to explore the effects of exosomes, secreted by retinal pigment epithelial (RPE) cells under oxidative stress (OS), on apoptosis and inflammation of normal RPE cells. Exosomes secreted by normal RPE cells (named as exo) and rotenone (2.5 µmol/L) stimulated RPE cells (named as rot‐exo) were isolated and extracted by multi‐step differential centrifugation for morphology observation under a transmission electron microscopy. pcDNA3.1a, pcDNA3.1a‐Apaf1, and p3xFlag‐CMV‐caspase‐9 plasmids were constructed and transfected into ARPE‐19 cells. Exosomes secreted by ARPE‐19 cells were injected into the vitreous body of rats to verify the effect of Apaf1 and caspase‐9 on cell apoptosis and inflammation. Co‐immunoprecipitation was applied to clarify the interaction of Apaf1 with caspase‐9. Exosomes secreted by rotenone stimulated ARPE‐19 cells could induce cell apoptosis, oxidative injury, and inflammation in ARPE‐19 cells. Exosomes secreted under OS can damage retinal functions of rats and have upregulated expression of Apaf1. Overexpression of Apaf1 in exosomes secreted under OS can cause the inhibition of cell proliferation, the increase of cell apoptosis and elicitation of inflammatory response in ARPE‐19 cells. Exosomes derived from ARPE‐19 cells under OS regulate Apaf1 expression to increase cell apoptosis and to induce oxidative injury and inflammatory response through a caspase‐9 apoptotic pathway.