An Essential Role for Histone Deacetylase 4 in Synaptic Plasticity and Memory Formation

被引:179
|
作者
Kim, Mi-Sung [2 ]
Akhtar, M. Waseem [1 ]
Adachi, Megumi [1 ]
Mahgoub, Melissa [1 ]
Bassel-Duby, Rhonda [2 ]
Kavalali, Ege T. [3 ]
Olson, Eric N. [2 ]
Monteggia, Lisa M. [1 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Dept Psychiat, Dallas, TX 75390 USA
[2] Univ Texas SW Med Ctr Dallas, Dept Mol Biol, Dallas, TX 75390 USA
[3] Univ Texas SW Med Ctr Dallas, Dept Neurosci, Dallas, TX 75390 USA
来源
JOURNAL OF NEUROSCIENCE | 2012年 / 32卷 / 32期
基金
美国国家卫生研究院;
关键词
CONTROLS CHONDROCYTE HYPERTROPHY; TRANSCRIPTION FACTOR; MOUSE MODEL; ANXIETY; RESPONSIVENESS; ACETYLATION; EXPRESSION; REPRESSION; INHIBITORS; AMYGDALA;
D O I
10.1523/JNEUROSCI.2089-12.2012
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Histone deacetylases (HDACs), a family of enzymes involved in epigenetic regulation, have been implicated in the control of synaptic plasticity, as well as learning and memory. Previous work has demonstrated administration of pharmacological HDAC inhibitors, primarily those targeted to class I HDACs, enhance learning and memory as well as long-term potentiation. However, a detailed understanding of the role of class II HDACs in these processes remains elusive. Here, we show that selective loss of Hdac4 in brain results in impairments in hippocampal-dependent learning and memory and long-term synaptic plasticity. In contrast, loss of Hdac5 does not impact learning and memory demonstrating unique roles in brain for individual class II HDACs. These findings suggest that HDAC4 is a crucial positive regulator of learning and memory, both behaviorally and at the cellular level, and that inhibition of Hdac4 activity may have unexpected detrimental effects to these processes.
引用
收藏
页码:10879 / 10886
页数:8
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