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组蛋白去乙酰化酶3(HDAC3)的去乙酰化酶结构域在海马体和内侧前额叶皮质的记忆形成与消退中发挥不同作用。

Distinct roles for the deacetylase domain of HDAC3 in the hippocampus and medial prefrontal cortex in the formation and extinction of memory.

作者信息

Alaghband Yasaman, Kwapis Janine L, López Alberto J, White André O, Aimiuwu Osasumwen V, Al-Kachak Amni, Bodinayake Kasuni K, Oparaugo Nicole C, Dang Richard, Astarabadi Mariam, Matheos Dina P, Wood Marcelo A

机构信息

301 Qureshey Research Lab, Department of Neurobiology and Behavior, Center for the Neurobiology of Learning and Memory, University of California, Irvine, Irvine, CA 92697, United States; Center for the Neurobiology of Learning and Memory (CNLM), Irvine, CA 92697, United States; Irvine Center for Addiction Neuroscience (ICAN), University of California, Irvine, CA 92697, United States.

301 Qureshey Research Lab, Department of Neurobiology and Behavior, Center for the Neurobiology of Learning and Memory, University of California, Irvine, Irvine, CA 92697, United States; Center for the Neurobiology of Learning and Memory (CNLM), Irvine, CA 92697, United States; Institute for Memory Impairments and Neurological Disorders, University of California, Irvine, Irvine, CA 92697, United States.

出版信息

Neurobiol Learn Mem. 2017 Nov;145:94-104. doi: 10.1016/j.nlm.2017.09.001. Epub 2017 Sep 8.

Abstract

Histone deacetylases (HDACs) are chromatin modifying enzymes that have been implicated as powerful negative regulators of memory processes. HDAC3has been shown to play a pivotal role in long-term memory for object location as well as the extinction of cocaine-associated memory, but it is unclear whether this function depends on the deacetylase domain of HDAC3. Here, we tested whether the deacetylase domain of HDAC3has a role in object location memory formation as well as the formation and extinction of cocaine-associated memories. Using a deacetylase-dead point mutant of HDAC3, we found that selectively blocking HDAC3 deacetylase activity in the dorsal hippocampus enhanced long-term memory for object location, but had no effect on the formation of cocaine-associated memory. When this same point mutant virus of HDAC3 was infused into the prelimbic cortex, it failed to affect cocaine-associated memory formation. With regards to extinction, impairing the HDAC3 deacetylase domain in the infralimbic cortex had no effect on extinction, but a facilitated extinction effect was observed when the point mutant virus was delivered to the dorsal hippocampus. These results suggest that the deacetylase domain of HDAC3 plays a selective role in specific brain regions underlying long-term memory formation of object location as well as cocaine-associated memory formation and extinction.

摘要

组蛋白脱乙酰酶(HDACs)是一类染色质修饰酶,被认为是记忆过程的强大负调控因子。HDAC3已被证明在物体位置的长期记忆以及可卡因相关记忆的消退中起关键作用,但尚不清楚该功能是否依赖于HDAC3的脱乙酰酶结构域。在这里,我们测试了HDAC3的脱乙酰酶结构域在物体位置记忆形成以及可卡因相关记忆的形成和消退中是否发挥作用。使用HDAC3的脱乙酰酶失活点突变体,我们发现选择性阻断背侧海马体中的HDAC3脱乙酰酶活性可增强物体位置的长期记忆,但对可卡因相关记忆的形成没有影响。当将相同的HDAC3点突变病毒注入前边缘皮层时,它未能影响可卡因相关记忆的形成。关于消退,损害边缘下皮层中的HDAC3脱乙酰酶结构域对消退没有影响,但当将点突变病毒传递到背侧海马体时,观察到促进消退的效果。这些结果表明,HDAC3的脱乙酰酶结构域在物体位置长期记忆形成以及可卡因相关记忆形成和消退的特定脑区中发挥选择性作用。

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