Mice deficient for the close homologue of the neural adhesion cell L1 (CHL1) display alterations in emotional reactivity and motor coordination

被引:40
作者
Pratte, M
Rougon, G
Schachner, M
Jamon, A
机构
[1] CNRS, Inst Neurosci Physiolog & Cognit, F-13402 Marseille 20, France
[2] NMDA, Inst Dev Biol, F-13288 Marseille, France
[3] Univ Hamburg, Zentrum Mol Neurobiol, D-20251 Hamburg, Germany
关键词
cell adhesion molecule; knock-out mice; exploratory behaviour; locomotor activity; cognitive deficit; 3p-syndrome;
D O I
10.1016/S0166-4328(03)00114-1
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Motor and cognitive phenotypes were assessed in mice deficient for the close homologue of the L1 adhesion molecule (CHL1). The CHL1-deficient mice displayed signs of decreased stress and a modification of exploratory behaviour. The mice also showed motor impairments on the Rotarod, but they were able to move as fast as controls in the alleys of a T-maze. The observed changes were assumed to be related to a deficit in attention. In addition, gender differences in CHL1 deficits were found and are discussed in view of a possible interaction with other cell adhesion molecules (CAMs) during development. The results are discussed in relation with motor and cognitive deficits in the human, caused by mutations of the distal part of the chromosome 3 which contains the CHL1 orthologue. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:31 / 39
页数:9
相关论文
共 40 条
[1]  
Angeloni D, 1999, AM J MED GENET, V86, P482, DOI 10.1002/(SICI)1096-8628(19991029)86:5<482::AID-AJMG15>3.0.CO
[2]  
2-L
[3]   RODENT SEX-DIFFERENCES IN EMOTIONAL AND RELATED BEHAVIOR [J].
ARCHER, J .
BEHAVIORAL BIOLOGY, 1975, 14 (04) :451-479
[4]   COMPARISON OF DIFFERENT BEHAVIORAL-TEST SITUATIONS USED IN PSYCHOPHARMACOLOGY FOR MEASUREMENT OF ANXIETY [J].
BELZUNG, C ;
LEPAPE, G .
PHYSIOLOGY & BEHAVIOR, 1994, 56 (03) :623-628
[5]   Ankyrins and cellular targeting of diverse membrane proteins to physiological sites [J].
Bennett, V ;
Chen, LS .
CURRENT OPINION IN CELL BIOLOGY, 2001, 13 (01) :61-67
[6]   Open-field behavior of house mice selectively bred for high voluntary wheel-running [J].
Bronikowski, AM ;
Carter, PA ;
Swallow, JG ;
Girard, IA ;
Rhodes, JS ;
Garland, T .
BEHAVIOR GENETICS, 2001, 31 (03) :309-316
[7]   Differences in measures of exploration and fear in MHC-congenic C57BL/6J and B6-H-2K mice [J].
Brown, RE ;
Corey, SC ;
Moore, AK .
BEHAVIOR GENETICS, 1999, 29 (04) :263-271
[8]   Neural cell recognition molecule L1:: from cell biology to human hereditary brain malformations [J].
Brümmendorf, T ;
Kenwrick, S ;
Rathjen, FG .
CURRENT OPINION IN NEUROBIOLOGY, 1998, 8 (01) :87-97
[9]   Analysis of the L1-deficient mouse phenotype reveals cross-talk between Sema3A and L1 signaling pathways in axonal guidance [J].
Castellani, V ;
Chédotal, A ;
Schachner, M ;
Faivre-Sarrailh, C ;
Rougon, G .
NEURON, 2000, 27 (02) :237-249
[10]   Cis and trans interactions of L1 with neuropilin-1 control axonal responses to semaphorin 3A [J].
Castellani, V ;
De Angelis, E ;
Kenwrick, S ;
Rougon, G .
EMBO JOURNAL, 2002, 21 (23) :6348-6357