Activity-Induced Nr4a1 Regulates Spine Density and Distribution Pattern of Excitatory Synapses in Pyramidal Neurons

被引:78
作者
Chen, Yelin [1 ]
Wang, Yuanyuan [1 ]
Ertuerk, Ali [1 ]
Kallop, Dara [2 ]
Jiang, Zhiyu [1 ]
Weimer, Robby M. [1 ,2 ]
Kaminker, Joshua [3 ]
Sheng, Morgan [1 ]
机构
[1] Genentech Inc, Dept Neurosci, San Francisco, CA 94080 USA
[2] Genentech Inc, Dept Biomed Imaging, San Francisco, CA 94080 USA
[3] Genentech Inc, Dept Bioinformat & Computat Biol, San Francisco, CA 94080 USA
关键词
LONG-TERM POTENTIATION; NUCLEAR ORPHAN RECEPTORS; DENDRITIC SPINES; SYNAPTIC PLASTICITY; NMDA RECEPTOR; EPILEPTIFORM ACTIVITY; TRANSCRIPTION FACTORS; HIPPOCAMPAL-NEURONS; ACTIN CYTOSKELETON; BINDING PROTEIN;
D O I
10.1016/j.neuron.2014.05.027
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Excitatory synapses occur mainly on dendritic spines, and spine density is usually correlated with the strength of excitatory synaptic transmission. We report that Nr4a1, an activity-inducible gene encoding a nuclear receptor, regulates the density and distribution of dendritic spines in CA1 pyramidal neurons. Nr4a1 overexpression resulted in elimination of the majority of spines; however, postsynaptic densities were preserved on dendritic shafts, and the strength of excitatory synaptic transmission was unaffected, showing that excitatory synapses can be dissociated from spines. mRNA expression profiling studies suggest that Nr4a1-mediated transcriptional regulation of the actin cytoskeleton contributes to this effect. Under conditions of chronically elevated activity, when Nr4a1 was induced, Nr4a1 knockdown increased the density of spines and PSDs specifically at the distal ends of dendrites. Thus, Nr4a1 is a key component of an activityinduced transcriptional program that regulates the density and distribution of spines and synapses.
引用
收藏
页码:431 / 443
页数:13
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