Long-term potentiation enhances neurogenesis in the adult dentate gyrus

被引:223
|
作者
Bruel-Jungerman, Elodie
Davis, Sabrina
Rampon, Claire
Laroche, Serge
机构
[1] Univ Paris Sud, Lab Neurol Apprentissage Memoire Commun, CNRS, UMR 8620, F-91405 Orsay, France
[2] Univ Toulouse 3, CNRS, Ctr Rech Cognit Anim, F-31062 Toulouse, France
来源
JOURNAL OF NEUROSCIENCE | 2006年 / 26卷 / 22期
关键词
synaptic plasticity; memory; hippocampus; cell survival; Zif268; transcription factor;
D O I
10.1523/JNEUROSCI.0782-06.2006
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Activity-dependent synaptic plasticity and neurogenesis are two forms of brain plasticity that can participate in functional remodeling of neural networks during the formation of memories. We examined whether long-term potentiation (LTP) of excitatory synaptic transmission, a well characterized form of synaptic plasticity believed to play a critical role in memory formation, can regulate the rate of neurogenesis in the adult rat dentate gyrus in vivo. We first show that induction of LTP at medial perforant path-granule cell synapses stimulates the proliferation of progenitor cells in the dentate gyrus with a consequential long-term persistence of a larger population of surviving newborn cells. Using protocols to examine the effect of LTP on survival, we next show that LTP induction promotes survival of 1- to 2-week-old dentate granule cells. In no case did LTP appear to affect neuronal differentiation. Finally, we show that LTP induces expression of the plasticity-related transcription factor Zif268 in a substantial fraction of 2-week-old but not 1-week-old neurons, suggesting the prosurvival effect of LTP can be observed in the absence of LTP-mediated Zif268 induction in newborn cells. Our results indicate that electrically induced LTP in the dentate gyrus in vivo provides a cellular/molecular environment that favors both proliferation and survival of adult-generated neurons.
引用
收藏
页码:5888 / 5893
页数:6
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