Excitation-neurogenesis coupling in adult neural stem/progenitor cells

被引:549
作者
Deisseroth, K [1 ]
Singla, S
Toda, H
Monje, M
Palmer, TD
Malenka, RC
机构
[1] Stanford Univ, Sch Med, Nancy Pritzker Lab, Dept Psychiat & Behav Sci, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Neurosurg, Stanford, CA 94305 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/S0896-6273(04)00266-1
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
A wide variety of in vivo manipulations influence neurogenesis in the adult hippocampus. It is not known, however, if adult neural stem/progenitor cells (NPCs) can intrinsically sense excitatory neural activity and thereby implement a direct coupling between excitation and neurogenesis. Moreover, the theoretical significance of activity-dependent neurogenesis in hippocampal-type memory processing networks has not been explored. Here we demonstrate that excitatory stimuli act directly on adult hippocampal NPCs to favor neuron production. The excitation is sensed via Ca(v)1.2/ 1.3 (L-type) Call channels and NMDA receptors on the proliferating precursors. Excitation through this pathway acts to inhibit expression of the glial fate genes Hes1 and Id2 and increase expression of NeuroD, a positive regulator of neuronal differentiation. These activity-sensing properties of the adult NPCs, when applied as an "excitation-neurogenesis coupling rule" within a Hebbian neural network, predict significant advantages for both the temporary storage and the clearance of memories.
引用
收藏
页码:535 / 552
页数:18
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