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本文引用的文献

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A Novel Retinal Oscillation Mechanism in an Autosomal Dominant Photoreceptor Degeneration Mouse Model.常染色体显性光感受器变性小鼠模型中的一种新型视网膜振荡机制。
Front Cell Neurosci. 2016 Jan 12;9:513. doi: 10.3389/fncel.2015.00513. eCollection 2015.
2
Increased phosphorylation of Cx36 gap junctions in the AII amacrine cells of RD retina.视网膜脱离(RD)视网膜的无长突细胞AII中Cx36缝隙连接的磷酸化增加。
Front Cell Neurosci. 2015 Oct 1;9:390. doi: 10.3389/fncel.2015.00390. eCollection 2015.
3
Morphology and function of three VIP-expressing amacrine cell types in the mouse retina.小鼠视网膜中三种表达血管活性肠肽的无长突细胞类型的形态与功能
J Neurophysiol. 2015 Oct;114(4):2431-8. doi: 10.1152/jn.00526.2015. Epub 2015 Aug 26.
4
Origins of spontaneous activity in the degenerating retina.退化视网膜中自发活动的起源。
Front Cell Neurosci. 2015 Jul 29;9:277. doi: 10.3389/fncel.2015.00277. eCollection 2015.
5
Specific wiring of distinct amacrine cells in the directionally selective retinal circuit permits independent coding of direction and size.方向选择性视网膜回路中不同无长突细胞的特定连接允许对方向和大小进行独立编码。
Neuron. 2015 Apr 8;86(1):276-91. doi: 10.1016/j.neuron.2015.02.035. Epub 2015 Mar 19.
6
Recording light-evoked postsynaptic responses in neurons in dark-adapted, mouse retinal slice preparations using patch clamp techniques.使用膜片钳技术在暗适应的小鼠视网膜切片标本中的神经元中记录光诱发的突触后反应。
J Vis Exp. 2015 Feb 11(96):52422. doi: 10.3791/52422.
7
An unconventional glutamatergic circuit in the retina formed by vGluT3 amacrine cells.由 vGluT3 无长突细胞形成的视网膜中一种非常规的谷氨酸能回路。
Neuron. 2014 Nov 19;84(4):708-15. doi: 10.1016/j.neuron.2014.10.021. Epub 2014 Nov 6.
8
Intrinsic bursting of AII amacrine cells underlies oscillations in the rd1 mouse retina.AII无长突细胞的内在爆发是rd1小鼠视网膜振荡的基础。
J Neurophysiol. 2014 Sep 15;112(6):1491-504. doi: 10.1152/jn.00437.2014. Epub 2014 Jul 9.
9
Network oscillations drive correlated spiking of ON and OFF ganglion cells in the rd1 mouse model of retinal degeneration.在视网膜变性的rd1小鼠模型中,网络振荡驱动ON和OFF神经节细胞的相关放电。
PLoS One. 2014 Jan 28;9(1):e86253. doi: 10.1371/journal.pone.0086253. eCollection 2014.
10
A method of horizontally sliced preparation of the retina.一种视网膜水平切片制备方法。
Methods Mol Biol. 2013;935:201-5. doi: 10.1007/978-1-62703-080-9_13.

去传入小鼠视网膜平铺标本中星爆无长突细胞的膜片钳记录

Patch Clamp Recording of Starburst Amacrine Cells in a Flat-mount Preparation of Deafferentated Mouse Retina.

作者信息

Tu Hung-Ya, Hsu Chih-Chun, Chen Yu-Jiun, Chen Ching-Kang

机构信息

Department of Ophthalmology, Baylor College of Medicine.

Department of Ophthalmology, Baylor College of Medicine; Department of Neuroscience, Baylor College of Medicine.

出版信息

J Vis Exp. 2016 Oct 13(116):54608. doi: 10.3791/54608.

DOI:10.3791/54608
PMID:27768050
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5092195/
Abstract

The mammalian retina is a layered tissue composed of multiple neuronal types. To understand how visual signals are processed within its intricate synaptic network, electrophysiological recordings are frequently used to study connections among individual neurons. We have optimized a flat-mount preparation for patch clamp recording of genetically marked neurons in both GCL (ganglion cell layer) and INL (inner nuclear layer) of mouse retinas. Recording INL neurons in flat-mounts is favored over slices because both vertical and lateral connections are preserved in the former configuration, allowing retinal circuits with large lateral components to be studied. We have used this procedure to compare responses of mirror-partnered neurons in retinas such as the cholinergic starburst amacrine cells (SACs).

摘要

哺乳动物的视网膜是一种由多种神经元类型组成的分层组织。为了了解视觉信号如何在其复杂的突触网络中进行处理,电生理记录经常被用于研究单个神经元之间的连接。我们优化了一种平铺标本制备方法,用于对小鼠视网膜神经节细胞层(GCL)和内核层(INL)中基因标记的神经元进行膜片钳记录。与切片相比,平铺标本记录INL神经元更具优势,因为在前者的配置中,垂直和横向连接都得以保留,从而能够研究具有大的横向成分的视网膜回路。我们已经使用这个程序来比较视网膜中镜像配对神经元的反应,比如胆碱能无长突星形细胞(SACs)。