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利用多特征视蛋白恢复患有视网膜变性的小鼠的视力。

Restoring vision in mice with retinal degeneration using multicharacteristic opsin.

作者信息

Wright Weldon, Gajjeraman Sivakumar, Batabyal Subrata, Pradhan Sanjay, Bhattacharya Sulagna, Mahapatra Vasu, Tripathy Ashutosh, Mohanty Samarendra

机构信息

NanoScope Technologies LLC, Bedford, Texas, United States.

出版信息

Neurophotonics. 2017 Oct;4(4):041412. doi: 10.1117/1.NPh.4.4.041412. Epub 2017 Aug 18.

Abstract

Retinal degenerative diseases, such as retinitis pigmentosa (RP) and dry age-related macular degeneration, have led to loss of vision in millions of individuals. Currently, no surgical or medical treatment is available, although optogenetic therapies are in clinical development. We demonstrate vision restoration using multicharacteristics opsin (MCO1) in animal models with degenerated retina. MCO1 is reliably delivered to specific retinal cells via intravitreal injection of adeno-associated virus (vMCO1), leading to significant improvement in visually guided behavior conducted using a radial arm water maze. The time to reach the platform and the number of error arms decreased significantly after delivery of MCO1. Notably, the improvement in visually guided behavior was observed even at light intensity levels orders of magnitude lower than that required for channelrhodopsin-2 opsin. Viability of vMCO1-treated retina is not compromised by chronic light exposure. Safe virus-mediated MCO1 delivery has potential for effective gene therapy of diverse retinal degenerations in patients.

摘要

视网膜退行性疾病,如色素性视网膜炎(RP)和干性年龄相关性黄斑变性,已导致数百万人视力丧失。目前,尚无手术或药物治疗方法,尽管光遗传学疗法正在临床开发中。我们在视网膜退化的动物模型中使用多特征视蛋白(MCO1)证明了视力恢复。通过玻璃体内注射腺相关病毒(vMCO1),MCO1可靠地递送至特定视网膜细胞,从而使使用放射状臂水迷宫进行的视觉引导行为有显著改善。在递送MCO1后,到达平台的时间和错误臂的数量显著减少。值得注意的是,即使在比通道视紫红质-2视蛋白所需光强度低几个数量级的光强度水平下,也观察到视觉引导行为的改善。vMCO1处理的视网膜的活力不会因长期光照而受损。安全的病毒介导的MCO1递送对患者各种视网膜退化进行有效基因治疗具有潜力。

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