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视网膜去传入对大鼠上丘表层中钙结合蛋白和小白蛋白免疫反应性神经元的年龄依赖性差异效应。

Differential age-dependent effects of retinal deafferentation upon calbindin- and parvalbumin-immunoreactive neurons in the superficial layers of the rat's superior colliculus.

作者信息

Lane R D, Allan D M, Bennett-Clarke C A, Rhoades R W

机构信息

Department of Anatomy and Neurobiology, Medical College of Ohio, Toledo 43699-0008, USA.

出版信息

Brain Res. 1996 Nov 18;740(1-2):208-14. doi: 10.1016/s0006-8993(96)00867-0.

DOI:10.1016/s0006-8993(96)00867-0
PMID:8973816
Abstract

Several recent studies have reported varied effects of different forms of visual deprivation on the expression of calcium-binding proteins in the CNS. Most of these studies have surveyed only a single protein from this family and have not systematically evaluated the influence of the age of the animal upon the effects observed. The present study combined immunocytochemistry and quantitative morphometry to determine the effects of eye removal in fetal life, at birth, or in adulthood upon the expression of calbindin and parvalbumin by neurons in the retinorecipient laminae (the stratum griseum superficiale (SGS) and stratum opticum (SO)) of the rat's superior colliculus (SC). Both fetal and neonatal enucleation significantly reduced the total number of neurons in the SGS. Eye removal at any age did not significantly affect the number of neurons in the SO or the proportion of SGS or SO cells that expressed calbindin. Adult enucleation produced a significant increase in the percentage of SGS cells expressing parvalbumin. These results suggest that calbindin expression is highly stable in visual neurons while parvalbumin expression is more plastic and appears to be suppressed by retinal input.

摘要

最近的几项研究报告了不同形式的视觉剥夺对中枢神经系统中钙结合蛋白表达的不同影响。这些研究大多只调查了该家族中的一种蛋白质,并且没有系统地评估动物年龄对所观察到的影响的作用。本研究结合免疫细胞化学和定量形态学方法,以确定在胎儿期、出生时或成年期摘除眼球对大鼠上丘(SC)视网膜接受层(浅灰质层(SGS)和视神经层(SO))中神经元表达钙结合蛋白和小白蛋白的影响。胎儿期和新生儿期摘除眼球均显著减少了SGS中的神经元总数。在任何年龄摘除眼球均未显著影响SO中的神经元数量,也未显著影响表达钙结合蛋白的SGS或SO细胞的比例。成年期摘除眼球使表达小白蛋白的SGS细胞百分比显著增加。这些结果表明,钙结合蛋白在视觉神经元中的表达高度稳定,而小白蛋白的表达更具可塑性,并且似乎受到视网膜输入的抑制。

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