Stromal-derived factor-1 (CXCL12) regulates laminar position of Cajal-Retzius cells in normal and dysplastic brains

被引:100
作者
Paredes, Mercedes F.
Li, Guangnan
Berger, Omri
Baraban, Scott C.
Pleasure, Samuel J. [1 ]
机构
[1] Univ Calif San Francisco, Neurosci Program, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Neurosurg, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Neurol, San Francisco, CA 94143 USA
关键词
lamination; cortex; cortical dysplasia; migration; marginal zone; teratogen;
D O I
10.1523/JNEUROSCI.2575-06.2006
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Normal brain development requires a series of highly complex and interrelated steps. This process presents many opportunities for errors to occur, which could result in developmental defects in the brain, clinically referred to as malformations of cortical development. The marginal zone and Cajal-Retzius cells are key players in cortical development and are established early, yet there is little understanding of the factors resulting in the disruption of the marginal zone in many types of cortical malformation syndromes. We showed previously that treatment with methylazoxymethanol in rats causes marginal zone dysplasia with displacement of Cajal-Retzius cells to deeper cortical layers. Here we establish that loss of activity of the chemokine stromal-derived factor-1 (SDF1) (CXCL12), which is expressed by the leptomeninges, is necessary and sufficient to cause marginal zone disorganization in this widely used teratogenic animal model. We also found that mice with mutations in the main receptor for SDF1 (CXCR4) have Cajal-Retzius cells displaced to deeper cortical layers. Furthermore, by inhibiting SDF1 signaling in utero by intraventricular injection of a receptor antagonist, we establish that SDF1 signaling is required for the maintenance of Cajal-Retzius cell position in the marginal zone during normal cortical development. Our data imply that cortical layering is not a static process, but rather requires input from locally produced molecular cues for maintenance, and that complex syndromes of cortical malformation as a result of environmental insults may still be amenable to explanation by interruption of specific molecular signaling pathways.
引用
收藏
页码:9404 / 9412
页数:9
相关论文
共 46 条
[1]   BDNF-modulated spatial organization of Cajal-Retzius and GABAergic neurons in the marginal zone plays a role in the development of cortical organization [J].
Alcántara, S ;
Pozas, E ;
Ibañez, CF ;
Soriano, E .
CEREBRAL CORTEX, 2006, 16 (04) :487-499
[2]  
Anton ES, 1997, DEVELOPMENT, V124, P3501
[3]  
Bagri A, 2002, DEVELOPMENT, V129, P4249
[4]   FAK deficiency in cells contributing to the basal lamina results in cortical abnormalities resembling congenital muscular dystrophies [J].
Beggs, HE ;
Schahin-Reed, D ;
Zang, KL ;
Goebbels, S ;
Nave, KA ;
Gorski, J ;
Jones, KR ;
Sretavan, D ;
Reichardt, LF .
NEURON, 2003, 40 (03) :501-514
[5]   The chemokine stromal cell-derived factor-1 regulates the migration of sensory neuron progenitors [J].
Belmadani, A ;
Tran, PB ;
Ren, DJ ;
Assimacopoulos, S ;
Grove, EA ;
Miller, RJ .
JOURNAL OF NEUROSCIENCE, 2005, 25 (16) :3995-4003
[6]   Multiple origins of Cajal-Retzius cells at the borders of the developing pallium [J].
Bielle, F ;
Griveau, A ;
Narboux-Nême, N ;
Vigneau, S ;
Sigrist, M ;
Arber, S ;
Wassef, M ;
Pierani, A .
NATURE NEUROSCIENCE, 2005, 8 (08) :1002-1012
[7]   Neuronal heterotopias in the developing cerebral cortex produced by neurotrophin-4 [J].
Brunstrom, JE ;
GraySwain, MR ;
Osborne, PA ;
Pearlman, AL .
NEURON, 1997, 18 (03) :505-517
[8]   AMD310, a small molecule inhibitor of HIV-1 entry via the CXCR4 co-receptor [J].
Donzella, GA ;
Schols, D ;
Lin, SW ;
Esté, JA ;
Nagashima, KA ;
Maddon, PJ ;
Allaway, GP ;
Sakmar, TP ;
Henson, G ;
De Clercq, E ;
Moore, JP .
NATURE MEDICINE, 1998, 4 (01) :72-77
[9]   Persistent reelin-expressing Cajal-Retzius cells in polymicrogyria [J].
Eriksson, SH ;
Thom, M ;
Heffernan, J ;
Lin, WR ;
Harding, BN ;
Squier, MV ;
Sisodiya, SM .
BRAIN, 2001, 124 :1350-1361
[10]   Cajal-Retzius cell density as marker of type of focal cortical dysplasia [J].
Garbelli, R ;
Frassoni, C ;
Ferrario, A ;
Tassi, L ;
Bramerio, M ;
Spreafico, R .
NEUROREPORT, 2001, 12 (12) :2767-2771