Activity-dependent dendritic arborization mediated by CaM-Kinase I activation and enhanced CREB-dependent transcription of Wnt-2

被引:383
作者
Wayman, Gary A.
Impey, Soren
Marks, Daniel
Saneyoshi, Takeo
Grant, Wilmon F.
Derkach, Victor
Soderling, Thomas R.
机构
[1] Oregon Hlth Sci Univ, Vollum Inst, Portland, OR 97239 USA
[2] Oregon Hlth Sci Univ, Oregon Stem Cell Ctr, Portland, OR 97239 USA
[3] Oregon Hlth Sci Univ, Ctr Study Weight Regulat, Portland, OR 97239 USA
关键词
D O I
10.1016/j.neuron.2006.05.008
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Members of the Wnt signaling family are important mediators of numerous developmental events, including activity-dependent dendrite development, but the pathways regulating expression and secretion of Wnt in response to neuronal activity are poorly defined. Here, we identify an NMDA receptor-mediated, Ca2+-dependent signaling pathway that couples neuronal activity to dendritic arborization through enhanced Wnt synthesis and secretion. Activity-dependent dendritic outgrowth and branching in cultured hippocampal neurons and slices is mediated through activation by CaM-dependent protein kinase kinase (CaMKK) of the membrane-associated gamma isoform of CaMKI. Downstream effectors of CaMKII include the MAP-kinase pathway of Ras/MEK/ERK and the transcription factor CREB. A serial analysis of chromatin occupancy screen identified Wnt-2 as an activity-dependent CREB-responsive gene. Neuronal activity enhances CREB-dependent transcription of Wnt-2, and expression of Wnt-2 stimulates dendritic arborization. This novel signaling pathway contributes to dynamic remodeling of the dendritic architecture in response to neuronal activity during development.
引用
收藏
页码:897 / 909
页数:13
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