Expression of neuronal nitric oxide synthase during embryonic development of the rat cerebral cortex

被引:52
作者
Santacana, M [1 ]
Uttenthal, LO [1 ]
Bentura, ML [1 ]
Fernández, AP [1 ]
Serrano, J [1 ]
de Velasco, JM [1 ]
Alonso, D [1 ]
Martínez-Murillo, R [1 ]
Rodrigo, J [1 ]
机构
[1] CSIC, Inst Cajal, E-28002 Madrid, Spain
来源
DEVELOPMENTAL BRAIN RESEARCH | 1998年 / 111卷 / 02期
关键词
neuronal nitric oxide synthase; nNOS; embryo; development; rat;
D O I
10.1016/S0165-3806(98)00140-0
中图分类号
Q [生物科学];
学科分类号
07 [理学]; 0710 [生物学]; 09 [农学];
摘要
The expression of neuronal nitric oxide synthase (nNOS) during the development of the rat cerebral cortex from embryonic day (E) 13 to postnatal day (P) 0 was analyzed by immunocytochemical procedures using a specific antibody against rat brain nNOS. Expression of nNOS was first seen on E14 in cells of Cajal-Retzius morphology located in the marginal zone. Neuronal NOS immunoreactivity persisted in this layer throughout the embryonic period and only began to decrease on E20, when neuronal migration is coming to an end. From E17 onwards, migrating neurons expressing nNOS were observed in the intermediate zone with their leading processes directed towards the cortical plate. Al the same time, efferent nNOS-immunoreactive axons originating from cortical plate cells entered the intermediate zone. From E19 onwards, cells expressing nNOS and with the morphological characteristics of migrating cells were observed in and near the subventricular zone. Confocal analysis of double immunostaining for nNOS and glial fibrillary acidic protein or nestin showed no coexpression of nNOS and glial markers in these cells, suggesting that nNOS-positive cells leaving the subventricular zone were not glial cells. Commissural, callosal and fimbrial fibers were seen to express nNOS on E18 and E19. This expression decreased from E20 and was very weak on E21 and P0. The observations suggest that nitric oxide is synthesized during embryonic life in relation to maturational processes such as the organization of cerebral lamination, and is involved in controlling migrational processes and fiber ingrowth. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:205 / 222
页数:18
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