Focal electrical stimulation of human retinal ganglion cells for vision restoration

Author:

Madugula Sasidhar SORCID,Gogliettino Alex RORCID,Zaidi MoosaORCID,Aggarwal GorishORCID,Kling AlexandraORCID,Shah Nishal PORCID,Brown Jeff BORCID,Vilkhu RamandeepORCID,Hays Madeline RORCID,Nguyen HuyORCID,Fan VictoriaORCID,Wu Eric GORCID,Hottowy PawelORCID,Sher AlexanderORCID,Litke Alan MORCID,Silva Ruwan A,Chichilnisky E JORCID

Abstract

Abstract Objective. Vision restoration with retinal implants is limited by indiscriminate simultaneous activation of many cells and cell types, which is incompatible with reproducing the neural code of the retina. Recent work has shown that primate retinal ganglion cells (RGCs), which transmit visual information to the brain, can be directly electrically activated with single-cell, single-spike, cell-type precision – however, this possibility has never been tested in the human retina. In this study we aim to characterize, for the first time, direct in situ extracellular electrical stimulation of individual human RGCs. Approach. Extracellular electrical stimulation of individual human RGCs was conducted in three human retinas ex vivo using a custom large-scale, multi-electrode array capable of simultaneous recording and stimulation. Measured activation properties were compared directly to extensive results from macaque. Main results. Precise activation was in many cases possible without activating overlying axon bundles, at low stimulation current levels similar to those used in macaque. The major RGC types could be identified and targeted based on their distinctive electrical signatures. The measured electrical activation properties of RGCs, combined with a dynamic stimulation algorithm, was sufficient to produce an evoked visual signal that was nearly optimal given the constraints of the interface. Significance. These results suggest the possibility of high-fidelity vision restoration in humans using bi-directional epiretinal implants.

Funder

National Eye Institute

John Chen

Polish National Science Centre

Stanford University School of Medicine

Wu Tsai Neurosciences Institute

Pew Charitable Trusts

Research to Prevent Blindness

Publisher

IOP Publishing

Subject

Cellular and Molecular Neuroscience,Biomedical Engineering

Reference45 articles.

1. Alterations of sodium and potassium channels of RGCs in RCS rat with the development of retinal degeneration;Chen;J. Mol. Neurosci.,2013

2. A simple white noise analysis of neuronal light responses;Chichilnisky;Network,2001

3. Functional asymmetries in ON and off ganglion cells of primate retina;Chichilnisky;J. Neurosci.,2002

4. Origins of perception: retinal ganglion cell diversity and the creation of praallel visual pathways;Dacey,2004

5. Mosaic arrangement of ganglion cell receptive fields in rabbit retina;Devries;J. Neurophysiol.,1997

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3