β-catenin is critical for dendritic morphogenesis

被引:400
作者
Yu, X [1 ]
Malenka, RC [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Psychiat & Behav Sci, Nancy Friend Pritzker Lab, Palo Alto, CA 94304 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/nn1132
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Regulated growth and arborization of dendritic processes are critical to the formation of functional neuronal networks. Here we identify beta-catenin as a critical mediator of dendritic morphogenesis. We found that increasing the intracellular levels of beta-catenin and other members of the cadherin/catenin complex, namely N-cadherin and N-catenin, enhances dendritic arborization in rat hippocampal neurons, an effect that does not require Wnt/beta-catenin-dependent transcription. Conversely, proteins that sequester beta-catenin decreased dendritic branch tip number and total dendritic branch length. Enhancement of dendritic growth elicited by depolarization requires beta-catenin and increased Wnt release. These results identify Wnt/beta-catenin signaling as an important mediator of dendritic development and suggest that the intracellular level of the cadherin/catenin complex is a limiting factor during critical stages of dendritic morphogenesis.
引用
收藏
页码:1169 / 1177
页数:9
相关论文
共 50 条
[1]  
Banker G., 1998, CULTURING NERVE CELL
[2]   T cell factor-activated transcription is not sufficient to induce anchorage-independent growth of epithelial cells expressing mutant β-catenin [J].
Barth, AIM ;
Stewart, DB ;
Nelson, WJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (09) :4947-4952
[3]  
Benson DL, 1998, J NEUROSCI, V18, P6892
[4]   Linking colorectal cancer to Wnt signaling [J].
Bienz, M ;
Clevers, H .
CELL, 2000, 103 (02) :311-320
[5]  
Brault V, 2001, DEVELOPMENT, V128, P1253
[6]   Wnt signaling: a common theme in animal development [J].
Cadigan, KM ;
Nusse, R .
GENES & DEVELOPMENT, 1997, 11 (24) :3286-3305
[7]   Regulation of cerebral cortical size by control of cell cycle exit in neural precursors [J].
Chenn, A ;
Walsh, CA .
SCIENCE, 2002, 297 (5580) :365-369
[8]   Dendritic arbor development and synaptogenesis [J].
Cline, HT .
CURRENT OPINION IN NEUROBIOLOGY, 2001, 11 (01) :118-126
[9]   Translocation of calmodulin to the nucleus supports CREB phosphorylation in hippocampal neurons [J].
Deisseroth, K ;
Heist, EK ;
Tsien, RW .
NATURE, 1998, 392 (6672) :198-202
[10]   DISRUPTION OF EPITHELIAL CELL-CELL ADHESION BY EXOGENOUS EXPRESSION OF A MUTATED NONFUNCTIONAL N-CADHERIN [J].
FUJIMORI, T ;
TAKEICHI, M .
MOLECULAR BIOLOGY OF THE CELL, 1993, 4 (01) :37-47