301. Starburst amacrine cells amplify optogenetic visual restoration through gap junctions
- Author
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Yusaku Katada, Hiromitsu Kunimi, Naho Serizawa, Deokho Lee, Kenta Kobayashi, Kazuno Negishi, Hideyuki Okano, Kenji F. Tanaka, Kazuo Tsubota, and Toshihide Kurihara
- Subjects
education.field_of_study ,Retina ,genetic structures ,Population ,Gap junction ,Channelrhodopsin ,Optogenetics ,Biology ,eye diseases ,Ganglion ,Cell biology ,Amacrine cell ,medicine.anatomical_structure ,Retinal ganglion cell ,medicine ,Genetics ,Molecular Medicine ,sense organs ,education ,Molecular Biology - Abstract
Ectopic induction of optogenetic actuators, such as channelrhodopsin, is a promising approach to restoring vision in the degenerating retina. However, the cell type-specific response of ectopic photoreception has not been well understood. It is limited to obtain efficient gene expression in a specifically targeted cell population by a transgenic approach. In the present study, we established a murine model with high efficiency of gene induction to retinal ganglion cells (RGCs)- and amacrine cells using an improved tetracycline transactivator-operator bipartite system (KENGE-tet system). To investigate the cell type-specific visual restorative effect, we expressed the channelrhodopsin gene into RGCs and amacrine cells using the KENGE-tet system. As a result, enhancement in the visual restorative effect was observed to RGCs and starburst amacrine cells. In conclusion, a photoresponse from amacrine cells may enhance the maintained response of RGCs and further increase/improve the visual restorative effect.
- Published
- 2023