Generation and behavioral characterization of β-catenin forebrain-specific conditional knock-out mice

被引:66
作者
Gould, Todd D. [1 ]
O'Donnell, Kelley C. [1 ]
Picchini, Alyssa M. [1 ]
Dow, Eliot R. [1 ]
Chen, Guang [1 ]
Manji, Husseini K. [1 ]
机构
[1] NIMH, Lab Mol Pathophysiol & Expt Therapeut, Natl Inst Hlth, Bethesda, MD USA
关键词
depression; bipolar disorder; mood; Wnt pathway; glycogen synthase kinase; behavior; mice;
D O I
10.1016/j.bbr.2007.12.028
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
The canonical Wnt pathway and beta-catenin have been implicated in the pathophysiology of mood disorders. We generated forebrain-specific CRE-mediated conditional P-catenin knock-out mice to begin exploring the behavioral implications of decreased Wnt pathway signaling in the central nervous system. In situ hybridization revealed a progressive knock-out of P-catenin that began between 2 and 4 weeks of age, and by 12 weeks resulted in considerably decreased P-catenin expression in regions of the forebrain, including the frontal cortex, hippocampus, and striatum. A significant decrease in protein levels of P-catenin in these brain regions was observed by Western blot. Behavioral characterization of these mice in several tests (including the forced swim test, tail suspension test (TST), learned helplessness, response and sensitization to stimulants, and light/dark box among other tests) revealed relatively circumscribed alterations. In the TST, knock-out mice spent significantly less time struggling (a depression-like phenotype). However, knock-out mice did not differ from their wild-type littermates in the other behavioral tests of mood-related or anxiety-related behaviors. These results suggest that a 60-70% beta-catenin reduction in circumscribed brain regions is only capable of inducing subtle behavioral changes. Alternatively, regulating P-catenin may modulate drug effects rather than being a model of mood disorder pathophysiology per se. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:117 / 125
页数:9
相关论文
共 41 条
[1]   beta-catenin is a target for the ubiquitin-proteasome pathway [J].
Aberle, H ;
Bauer, A ;
Stappert, J ;
Kispert, A ;
Kemler, R .
EMBO JOURNAL, 1997, 16 (13) :3797-3804
[2]   Antipsychotics alter the protein expression levels of β-catenin and GSK-3 in the rat medial prefrontal cortex and striatum [J].
Alimohamad, H ;
Rajakumar, N ;
Seah, YH ;
Rushlow, W .
BIOLOGICAL PSYCHIATRY, 2005, 57 (05) :533-542
[3]   Lithium antagonizes dopamine-dependent behaviors mediated by an AKT/glycogen synthase kinase 3 signaling cascade [J].
Beaulieu, JM ;
Sotnikova, TD ;
Yao, WD ;
Kockeritz, L ;
Woodgett, JR ;
Gainetdinov, RR ;
Caron, MG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (14) :5099-5104
[4]   Functional interaction of an axin homolog, conductin, with β-catenin, APC, and GSK3β [J].
Behrens, J ;
Jerchow, BA ;
Würtele, M ;
Grimm, J ;
Asbrand, C ;
Wirtz, R ;
Kühl, M ;
Wedlich, D ;
Birchmeier, W .
SCIENCE, 1998, 280 (5363) :596-599
[5]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[6]  
Brault V, 2001, DEVELOPMENT, V128, P1253
[7]   The mood-stabilizing agent valproate inhibits the activity of glycogen synthase kinase-3 [J].
Chen, G ;
Huang, LD ;
Jiang, YM ;
Manji, HK .
JOURNAL OF NEUROCHEMISTRY, 1999, 72 (03) :1327-1330
[8]  
CRAWLEY JN, 2000, WHATS WRONG MY MOUSE, V13, P329
[9]   The tail suspension test as a model for assessing antidepressant activity: Review of pharmacological and genetic studies in mice [J].
Cryan, JF ;
Mombereau, C ;
Vassout, A .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 2005, 29 (4-5) :571-625
[10]   Antidepressant-like effects in various mice strains in the forced swimming test [J].
David, DJP ;
Renard, CE ;
Jolliet, P ;
Hascoët, M ;
Bourin, M .
PSYCHOPHARMACOLOGY, 2003, 166 (04) :373-382