Distribution of mRNA for the α4 subunit of the nicotinic acetylcholine receptor in the human fetal brain

被引:35
作者
Agulhon, C
Charnay, Y
Vallet, P
Bertrand, D
Malafosse, A
机构
[1] Hop Univ Geneve, Dept Psychiat, Div Neuropsychiat, CH-1225 Geneva, Switzerland
[2] Univ Geneva, Ctr Med Univ, Dept Physiol, CH-1211 Geneva, Switzerland
来源
MOLECULAR BRAIN RESEARCH | 1998年 / 58卷 / 1-2期
关键词
nicotinic acetylcholine receptor; alpha; 4; subunit; human fetal brain; in situ hybridization; anatomical localization; fragile X syndrome;
D O I
10.1016/S0169-328X(98)00113-2
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Neuronal nicotinic acetylcholine receptors (nAChRs) present in the central nervous system (CNS), are multimeric proteins constituted of two different subunits, alpha and beta, with different subtype arrangements and different pharmacological and functional properties. By in situ hybridization, we studied the distribution of the mRNA for the alpha 4 subunit of nAChRs in brains of human 25-week old normal and fragile X fetuses. A strong hybridization signal was detected throughout the thalamus, cortex, pyramidal layer of the Ammon's hem, and the granular layer of the dentate gyrus. Several other areas including the claustrum, caudate nucleus, putamen, globus pallidus, subthalamic nucleus, subiculum, entorhinal cortex, and Purkinje cell layer displayed a low to moderate radiosignal. With few exceptions, our data in the human brain agree those previously reported in the rat. Also, our data indicate that the alpha 4 subunit mRNA is produced early in the development, in the more differentiated cells, and in a site-specific manner. Additionally, the alpha 4 mRNA is produced in the brain of fragile X fetuses with the same pattern and same intensity than in the normal fetal brain suggesting that alpha 4 subunit mRNA production is not altered in the fragile X syndrome. High levels of alpha 4 subunit mRNA in human fetal brain support the hypothesis of a morphogenic role of nAChRs during the early CNS development. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:123 / 131
页数:9
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