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本文引用的文献

1
In Vivo Two-Photon Fluorescence Kinetics of Primate Rods and Cones.灵长类视杆细胞和视锥细胞的体内双光子荧光动力学
Invest Ophthalmol Vis Sci. 2016 Feb;57(2):647-57. doi: 10.1167/iovs.15-17946.
2
Two-Photon Autofluorescence Imaging Reveals Cellular Structures Throughout the Retina of the Living Primate Eye.双光子自发荧光成像揭示了活体灵长类动物眼睛整个视网膜中的细胞结构。
Invest Ophthalmol Vis Sci. 2016 Feb;57(2):632-46. doi: 10.1167/iovs.15-17961.
3
Advances in retinal ganglion cell imaging.视网膜神经节细胞成像的进展。
Eye (Lond). 2015 Oct;29(10):1260-9. doi: 10.1038/eye.2015.154. Epub 2015 Aug 21.
4
Cone and rod loss in Stargardt disease revealed by adaptive optics scanning light ophthalmoscopy.自适应光学扫描激光检眼镜揭示的斯塔加特病中的视锥和视杆细胞丢失
JAMA Ophthalmol. 2015 Oct;133(10):1198-203. doi: 10.1001/jamaophthalmol.2015.2443.
5
Distinctive receptive field and physiological properties of a wide-field amacrine cell in the macaque monkey retina.猕猴视网膜中一种广域无长突细胞的独特感受野和生理特性。
J Neurophysiol. 2015 Sep;114(3):1606-16. doi: 10.1152/jn.00484.2015. Epub 2015 Jul 1.
6
An adaptive optics imaging system designed for clinical use.一种专为临床应用设计的自适应光学成像系统。
Biomed Opt Express. 2015 May 18;6(6):2120-37. doi: 10.1364/BOE.6.002120. eCollection 2015 Jun 1.
7
Calibration-free sinusoidal rectification and uniform retinal irradiance in scanning light ophthalmoscopy.扫描激光检眼镜中无校准正弦整流与均匀视网膜辐照度
Opt Lett. 2015 Jan 1;40(1):85-8. doi: 10.1364/OL.40.000085.
8
Closed-loop optical stabilization and digital image registration in adaptive optics scanning light ophthalmoscopy.自适应光学扫描激光检眼镜中的闭环光学稳定与数字图像配准
Biomed Opt Express. 2014 Aug 26;5(9):3174-91. doi: 10.1364/BOE.5.003174. eCollection 2014 Sep 1.
9
Endogenous fluorophores enable two-photon imaging of the primate eye.内源性荧光团可实现灵长类动物眼睛的双光子成像。
Invest Ophthalmol Vis Sci. 2014 Jun 26;55(7):4438-47. doi: 10.1167/iovs.14-14395.
10
Photoreceptor perturbation around subretinal drusenoid deposits as revealed by adaptive optics scanning laser ophthalmoscopy.自适应光学扫描激光检眼镜揭示的视网膜下类玻璃膜疣沉积物周围的光感受器扰动
Am J Ophthalmol. 2014 Sep;158(3):584-96.e1. doi: 10.1016/j.ajo.2014.05.038. Epub 2014 Jun 5.

对活体眼睛视网膜神经节细胞层中的单个神经元进行成像。

Imaging individual neurons in the retinal ganglion cell layer of the living eye.

作者信息

Rossi Ethan A, Granger Charles E, Sharma Robin, Yang Qiang, Saito Kenichi, Schwarz Christina, Walters Sarah, Nozato Koji, Zhang Jie, Kawakami Tomoaki, Fischer William, Latchney Lisa R, Hunter Jennifer J, Chung Mina M, Williams David R

机构信息

Center for Visual Science, University of Rochester, Rochester, NY 14642;

Center for Visual Science, University of Rochester, Rochester, NY 14642.

出版信息

Proc Natl Acad Sci U S A. 2017 Jan 17;114(3):586-591. doi: 10.1073/pnas.1613445114. Epub 2017 Jan 3.

DOI:10.1073/pnas.1613445114
PMID:28049835
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5255596/
Abstract

Although imaging of the living retina with adaptive optics scanning light ophthalmoscopy (AOSLO) provides microscopic access to individual cells, such as photoreceptors, retinal pigment epithelial cells, and blood cells in the retinal vasculature, other important cell classes, such as retinal ganglion cells, have proven much more challenging to image. The near transparency of inner retinal cells is advantageous for vision, as light must pass through them to reach the photoreceptors, but it has prevented them from being directly imaged in vivo. Here we show that the individual somas of neurons within the retinal ganglion cell (RGC) layer can be imaged with a modification of confocal AOSLO, in both monkeys and humans. Human images of RGC layer neurons did not match the quality of monkey images for several reasons, including safety concerns that limited the light levels permissible for human imaging. We also show that the same technique applied to the photoreceptor layer can resolve ambiguity about cone survival in age-related macular degeneration. The capability to noninvasively image RGC layer neurons in the living eye may one day allow for a better understanding of diseases, such as glaucoma, and accelerate the development of therapeutic strategies that aim to protect these cells. This method may also prove useful for imaging other structures, such as neurons in the brain.

摘要

尽管采用自适应光学扫描光检眼镜(AOSLO)对活体视网膜进行成像可实现对单个细胞的微观观察,比如光感受器、视网膜色素上皮细胞以及视网膜血管系统中的血细胞,但事实证明,对其他重要细胞类别(如视网膜神经节细胞)进行成像则困难得多。视网膜内层细胞近乎透明,这对视觉有益,因为光线必须穿过它们才能抵达光感受器,但这也使得它们无法在活体中直接成像。在此,我们表明,通过对共焦AOSLO进行改进,可对猴子和人类视网膜神经节细胞(RGC)层内的神经元个体胞体进行成像。由于包括安全顾虑限制了人体成像允许的光强度等多种原因,人类RGC层神经元的图像质量不及猴子图像。我们还表明,将同样的技术应用于光感受器层,能够解决年龄相关性黄斑变性中视锥细胞存活情况的模糊问题。在活体眼中对RGC层神经元进行无创成像的能力,或许有朝一日能让人更好地了解青光眼等疾病,并加速旨在保护这些细胞的治疗策略的研发。该方法可能对成像其他结构(如大脑中的神经元)也有用处。