| Literature DB >> 34201658 |
Kitako Tabata1, Eriko Sugano1, Akito Hatakeyama1, Yoshito Watanabe1, Tomoya Suzuki1, Taku Ozaki1, Tomokazu Fukuda1, Hiroshi Tomita1,2.
Abstract
The death of photoreceptor cells is induced by continuous light exposure. However, it is unclear whether light damage was induced in retinal ganglion cells with photosensitivity by transduction of optogenetic genes. In this study, we evaluated the phototoxicities of continuous light exposure on retinal ganglion cells after transduction of the optogenetic gene mVChR1 using an adeno-associated virus vector. Rats were exposed to continuous light for a week, and visually evoked potentials (VEPs) were recorded. The intensities of continuous light (500, 1000, 3000, and 5000 lx) increased substantially after VEP recordings. After the final recording of VEPs, retinal ganglion cells (RGCs) were retrogradely labeled with a fluorescein tracer, FluoroGold, and the number of retinal ganglion cells was counted under a fluorescent microscope. There was no significant reduction in the amplitudes of VEPs and the number of RGCs after exposure to any light intensity. These results indicated that RGCs were photosensitive after the transduction of optogenetic genes and did not induce any phototoxicity by continuous light exposure.Entities:
Keywords: channelrhodopsin; gene therapy; light damage; retinal ganglion cells; retinitis pigmentosa
Year: 2021 PMID: 34201658 DOI: 10.3390/ijms22136732
Source DB: PubMed Journal: Int J Mol Sci ISSN: 1422-0067 Impact factor: 5.923