Restoring light sensitivity using tunable near-infrared sensors

被引:78
|
作者
Nelidova, Dasha [1 ,2 ]
Morikawa, Rei K. [1 ,2 ]
Cowan, Cameron S. [1 ,2 ]
Raics, Zoltan [1 ,2 ]
Goldblum, David [3 ]
Scholl, Hendrik P. N. [1 ,3 ,4 ]
Szikra, Tamas [1 ,2 ]
Szabo, Arnold [5 ]
Hillier, Daniel [1 ,2 ,6 ,7 ,8 ]
Roska, Botond [1 ,2 ,3 ]
机构
[1] Inst Mol & Clin Ophthalmol Basel, Basel, Switzerland
[2] Friedrich Miescher Inst Biomed Res, Basel, Switzerland
[3] Univ Basel, Dept Ophthalmol, Basel, Switzerland
[4] Johns Hopkins Univ, Wilmer Eye Inst, Baltimore, MD 21218 USA
[5] Semmelweis Univ, Dept Anat, Budapest, Hungary
[6] Leibniz Inst Primate Res, Deutsch Primatzentrum, Gottingen, Germany
[7] Res Ctr Nat Sci, Budapest, Hungary
[8] Pazmany Peter Catholic Univ, Fac Informat Technol & Bion, Budapest, Hungary
基金
欧洲研究理事会; 瑞士国家科学基金会;
关键词
GOLD NANOPARTICLES; NEOVASCULARIZATION; ANTIBODIES; RESPONSES; CELLS;
D O I
10.1126/science.aaz5887
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Enabling near-infrared light sensitivity in a blind human retina may supplement or restore visual function in patients with regional retinal degeneration. We induced near-infrared light sensitivity using gold nanorods bound to temperature-sensitive engineered transient receptor potential (TRP) channels. We expressed mammalian or snake TRP channels in light-insensitive retinal cones in a mouse model of retinal degeneration. Near-infrared stimulation increased activity in cones, ganglion cell layer neurons, and cortical neurons, and enabled mice to perform a learned light-driven behavior. We tuned responses to different wavelengths, by using nanorods of different lengths, and to different radiant powers, by using engineered channels with different temperature thresholds. We targeted TRP channels to human retinas, which allowed the postmortem activation of different cell types by near-infrared light.
引用
收藏
页码:1108 / +
页数:39
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