Mitochondrial Protection by Exogenous Otx2 in Mouse Retinal Neurons

OTX2 (orthodenticle homeobox 2) haplodeficiency causes diverse defects in mammalian visual systems ranging from retinal dysfunction to anophthalmia. We find that the retinal dystrophy of Otx2+/GFP heterozygous knockin mice is mainly due to the loss of bipolar cells and consequent deficits in retinal activity. Among bipolar cell types, OFF-cone bipolar subsets, which lack autonomous Otx2 gene expression but receive Otx2 proteins from photoreceptors, degenerate most rapidly in Otx2+/GFP mouse retinas, suggesting a neuroprotective effect of the imported Otx2 protein. In support of this hypothesis, retinal dystrophy in Otx2+/GFP mice is prevented by intraocular injection of Otx2 protein, which localizes to the mitochondria of bipolar cells and facilitates ATP synthesis as a part of mitochondrial ATP synthase complex. Taken together, our findings demonstrate a mitochondrial function for Otx2 and suggest a potential therapeutic application of OTX2 protein delivery in human retinal dystrophy. [Display omitted] •Otx2 haplodeficiency results in retinal dystrophy in mice•Otx2 proteins from photoreceptors are protective of retinal bipolar cells•Exogenous Otx2 in bipolar cells is found into mitochondria and affects ATP synthesis•Intraocular Otx2 injection restores retinal activity in Otx2−/+ mice Kim et al. propose a neuroprotective activity for exogenous OTX2 in mitochondria of retinal bipolar cells. The authors suggest that retinal dystrophy in OTX2-haplodeficient humans and mice is related to a decrease in the amount of OTX2 protein transferred to retinal bipolar cells.