Preparation of embryonic retinal explants to study CNS neurite growth

被引:7
作者
Hanea, Sonia T. [1 ]
Shanmugalingam, Ushananthini [1 ]
Fournier, Alyson E. [2 ]
Smith, Patrice D. [1 ]
机构
[1] Carleton Univ, Dept Neurosci, 1125 Colonel By Dr, Ottawa, ON K1S 5B6, Canada
[2] McGill Univ, Montreal Neurol Inst, Dept Neurol & Neurosurg, BT-109,3801 Rue Univ, Montreal, PQ H3A 2B4, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Retinal explant; Retinal ganglion cell; Neurite growth; GANGLION-CELLS; AXON REGENERATION; OPTIC-NERVE; ORGANOTYPIC CULTURE; PROGENITOR CELLS; CONE COLLAPSE; ADULT-RATS; IN-VIVO; MOUSE; NEURONS;
D O I
10.1016/j.exer.2016.04.004
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
This protocol outlines the preparation of embryonic mouse retinal explants, which provides an effective technique to analyze neurite outgrowth in central nervous system (CNS) neurons. This validated ex vivo system, which displays limited neuronal death, is highly reproducible and particularly amenable to manipulation. Our previously published studies involving embryonic chick or adult mouse retinal ex plants were instrumental in the preparation of this protocol; aspects of these previous techniques were combined, adopted and optimized. This protocol thus permits more efficient analysis of neurite growth. Briefly, the retina is dissected from the embryonic mouse eye using precise techniques that take into account the small size of the embryonic eye. The approach applied ensures that the retinal ganglion cell (RGC) layer faces the adhesion substrate on coated cover slips. Neurite growth is clear, well-delineated and readily quantifiable. These retinal explants can therefore be used to examine the neurite growth effects elicited by potential therapeutic agents. (c) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:304 / 312
页数:9
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