Increased sensitivity to myopia and altered retinal ON/OFF balance in a mouse model lacking Dusp4

Abstract Myopia, influenced by environmental and genetic factors, occurs when the emmetropization process fails to stop, causing excessive eyeball growth. Highly myopic animal models lacking a functional ON-pathway identified Dusp4 as a potential gene implicated in myopia. Here, we use a mouse model lacking DUSP4 to gain a better understanding of its retinal role and the mechanisms implicated in myopia development. Dusp4−/− mice have a reduced basal level of retinal dopamine and a higher susceptibility to lens-induced myopia. Dusp4 is expressed in ON-bipolar cells and a subset of OFF-bipolar cells in a light dependent manner. The absence of DUSP4 causes a hyperactivation of the MAPK/ERK pathway. Dusp4−/− mice show a reduced optomotor response, increased ON-bipolar cell responses, reduced oscillatory potentials together with altered OFF and ON-OFF RGC response to light flashes. These data provide new insights into retina-driven mechanisms of myopization, nuancing the impact of ON and OFF pathways upon emmetropization. Competing Interest Statement The authors have declared no competing interest. Footnotes Competing Interest Statement: The authors have no competing interest to declare. Some funding informations and authorship informations were added