Program in Neurosciences and Mental Health, Hospital for Sick Children, Toronto, ON, Canada M5G 1X8.
Proc Natl Acad Sci U S A. 2011 May 17;108(20):8456-60. doi: 10.1073/pnas.1016275108. Epub 2011 Apr 29.
Remodeling of cortical connectivity is thought to allow initially hippocampus-dependent memories to be expressed independently of the hippocampus at remote time points. Consistent with this, consolidation of a contextual fear memory is associated with dendritic spine growth in neurons of the anterior cingulate cortex (aCC). To directly test whether such cortical structural remodeling is necessary for memory consolidation, we disrupted spine growth in the aCC at different times following contextual fear conditioning in mice. We took advantage of previous studies showing that the transcription factor myocyte enhancer factor 2 (MEF2) negatively regulates spinogenesis both in vitro and in vivo. We found that increasing MEF2-dependent transcription in the aCC during a critical posttraining window (but not at later time points) blocked both the consolidation-associated dendritic spine growth and subsequent memory expression. Together, these data strengthen the causal link between cortical structural remodeling and memory consolidation and, further, identify MEF2 as a key regulator of these processes.
皮质连接的重塑被认为可以使最初依赖海马体的记忆在远程时间点独立于海马体表达。与此一致的是,情境性恐惧记忆的巩固与扣带前皮质(aCC)神经元中的树突棘生长有关。为了直接测试这种皮质结构重塑是否对记忆巩固是必要的,我们在小鼠进行情境性恐惧条件反射后的不同时间破坏 aCC 中的棘突生长。我们利用先前的研究结果表明,转录因子肌细胞增强因子 2(MEF2)在体外和体内都能负调控棘突生成。我们发现,在关键的训练后窗口(而不是在稍后的时间点)增加 aCC 中 MEF2 依赖性转录会阻止与巩固相关的树突棘生长和随后的记忆表达。这些数据共同加强了皮质结构重塑与记忆巩固之间的因果关系,并进一步确定 MEF2 是这些过程的关键调节因子。