NMDA receptor-independent control of transcription factors and gene expression

被引:11
作者
Adams, J. Paige [1 ]
Robinson, Rachel A. [1 ]
Hudgins, Eric D. [1 ]
Wissink, Erin M. [1 ]
Dudek, Serena M. [1 ]
机构
[1] NIEHS, Neurobiol Lab, NIH, Res Triangle Pk, NC 27709 USA
基金
美国国家卫生研究院;
关键词
action potential; arc/Arg3.1; calcium; CREB; long-term potentiation; hippocampus; LONG-TERM POTENTIATION; REGULATED KINASE ACTIVATION; LATE-PHASE; HIPPOCAMPAL-NEURONS; MESSENGER-RNA; CONSOLIDATION; ARC/ARG3.1; INDUCTION; ARC; LTP;
D O I
10.1097/WNR.0b013e3283311db6
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Consolidation of synaptic plasticity seems to require transcription, but how the nucleus is informed in this context remains unknown. As NMDA receptor antagonists have been shown to interfere with action potential generation, the issue of whether or not a synaptically generated signal is required for nuclear signaling is currently unresolved. Here, we show that pharmacological maintenance of action potentials during NMDA receptor blockade allows for NMDA receptor-independent transcription factor binding and arc gene expression, both of which were previously thought to be NMDA receptor dependent. These data suggest that types of signaling in the nucleus previously attributed to NMDA-receptor-dependent synapse-to-nucleus signals can be initiated in the absence of NMDA receptor-dependent synaptic plasticity. NeuroReport 20:1429-1433 (C) 2009 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins.
引用
收藏
页码:1429 / 1433
页数:5
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