Early serotonergic projections to Cajal-Retzius cells: Relevance for cortical development

被引:110
作者
Janusonis, S [1 ]
Gluncic, V [1 ]
Rakic, P [1 ]
机构
[1] Yale Univ, Sch Med, Dept Neurobiol, New Haven, CT 06520 USA
关键词
serotonin (5-HT); Cajal-Retzius cells; reelin; autism; microcolumns; marginal zone;
D O I
10.1523/JNEUROSCI.4651-03.2004
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Although the serotonergic system plays an important role in various neurological disorders, the role of early serotonergic projections to the developing cerebral cortex is not well understood. Because serotonergic fibers enter the marginal zone (MZ) before birth, it has been suggested that they may influence cortical development through synaptic contacts with Cajal-Retzius (CR) cells. We used immunohistochemistry combined with confocal and electron microscopy to show that the earliest serotonergic projections to the MZ form synaptic contacts with the somata and proximal dendrites of CR cells as early as embryonic day 17. To elucidate the functional significance of these early serotonergic contacts with CR cells, we perturbed their normal development by injecting pregnant mice with 5-methoxytryptamine. Lower reelin levels were detected in the brains of newborn pups from the exposed animals. Because reelin plays an important role in the cortical laminar and columnar organization during development, we killed some pups from the same litters on postnatal day 7 and analyzed their presubicular cortex. We found that the supragranular layers of the presubicular cortex (which normally display a visible columnar deployment of neurons) were altered in the treated animals. Our results suggest a mechanism of how serotonergic abnormalities during cortical development may disturb the normal cortical organization; and, therefore, may be relevant for understanding neurological disorders in which abnormalities of the serotonergic system are accompanied by cortical pathology ( such as autism).
引用
收藏
页码:1652 / 1659
页数:8
相关论文
共 76 条
[1]  
Alcántara S, 1998, J NEUROSCI, V18, P7779
[2]  
Anderson GM, 1990, ANN N Y ACAD SCI, V600, p[331, 341]
[3]  
Ang ESBC, 2003, J NEUROSCI, V23, P5805
[4]   Modern views on an ancient chemical: Serotonin effects on cell proliferation, maturation, and apoptosis [J].
Azmitia, EC .
BRAIN RESEARCH BULLETIN, 2001, 56 (05) :413-424
[5]   FETAL HUMAN BRAIN EXHIBITS A PRENATAL PEAK IN THE DENSITY OF SEROTONIN 5-HT1A RECEPTORS [J].
BARPELED, O ;
GROSSISSEROFF, R ;
BENHUR, H ;
HOSKINS, I ;
GRONER, Y ;
BIEGON, A .
NEUROSCIENCE LETTERS, 1991, 127 (02) :173-176
[6]   Prenatal development of the serotonin transporter in mouse brain [J].
Bruning, G ;
Liangos, O ;
Baumgarten, HG .
CELL AND TISSUE RESEARCH, 1997, 289 (02) :211-221
[7]   Reduced interneuronal space in schizophrenia [J].
Buxhoeveden, D ;
Roy, E ;
Switala, A ;
Casanova, MF .
BIOLOGICAL PSYCHIATRY, 2000, 47 (07) :681-682
[8]   Quantitative analysis of cell columns in the cerebral cortex [J].
Buxhoeveden, DP ;
Switala, AE ;
Roy, E ;
Casanova, MF .
JOURNAL OF NEUROSCIENCE METHODS, 2000, 97 (01) :7-17
[9]   The minicolumn hypothesis in neuroscience [J].
Buxhoeveden, DP ;
Casanova, MF .
BRAIN, 2002, 125 :935-951
[10]   Modular concepts of brain organization and the neuropathology of psychiatric conditions [J].
Casanova, MF .
PSYCHIATRY RESEARCH, 2003, 118 (01) :101-102