Age-related macular degeneration (AMD) is a common degenerative eye disease that eventually leads to irreversible vision loss. CircRNAs have received increasing attention for their regulatory role in AMD. In this study, whole transcriptome sequencing identified differentially expressed circRNA (circMETTL3) in AMD. Previous studies have unlocked the potential mechanism of circMETTL3 in cancer, but its role in AMD has not been studied. ARPE-19 cells treated with H2O2 were used as the AMD cell model. The senescence, oxidative stress, and DNA damage of ARPE-19 cells were determined by SA-b-gal staining, DCFH-DA staining, and IF assay. The levels of RPE-specific markers or mRNA levels were assessed using western blot assay. The potential mechanism of circMETTL3 was investigated by luciferase reporting assay and RIP assay. CircMETTL3 was revealed to decrease in AMD cell models. The addition of circMETTL3 decreased SA-b-gal staining and ROS production and facilitated cell viability in H2O2-treated ARPE-19 cells. Moreover, γH2AX level was suppressed, and TJP1, BEST1 and CTNNB1 protein levels were increased by circMETTL3 addition. In addition, circMETTL3 could bind to and negatively regulate miR-100. miR-100 silencing reduced senescence, oxidative stress, and DNA damage in H2O2-treated ARPE-19 cells. Furthermore, BMPR2 was targeted by miR-100. Inhibition of BMPR2 promoted H2O2-induced cell damage in ARPE-19 cells. In sum, these findings demonstrated that the circMETTL3/miR-100/BMPR2 axis plays a vital regulatory role in AMD development.