Lubin Farah D, Sweatt J David
The Evelyn F. McKnight Brain Institute, Department of Neurobiology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Neuron. 2007 Sep 20;55(6):942-57. doi: 10.1016/j.neuron.2007.07.039.
Previously formed memories are susceptible to disruption immediately after recall due to a necessity to be reconsolidated after retrieval. Protein translation mechanisms have been widely implicated as being necessary for memory reconsolidation, but gene transcription mechanisms have been much less extensively studied in this context. We found that retrieval of contextual conditioned fear memories activates the NF-kappaB pathway to regulate histone H3 phosphorylation and acetylation at specific gene promoters in hippocampus, specifically via IKKalpha and not the NF-kappaB DNA-binding complex. Behaviorally, we found that inhibition of IKKalpha regulation of either chromatin structure or NF-kappaB DNA-binding complex activity leads to impairments in fear memory reconsolidation, and that elevating histone acetylation rescues this memory deficit in the face of IKK blockade. These data provide insights into IKK-regulated transcriptional mechanisms in hippocampus that are necessary for memory reconsolidation.
先前形成的记忆在回忆后会立即受到干扰,因为在检索后需要重新巩固。蛋白质翻译机制已被广泛认为是记忆重新巩固所必需的,但在这种情况下,基因转录机制的研究却少得多。我们发现,情境性条件恐惧记忆的检索会激活NF-κB通路,以调节海马体中特定基因启动子处组蛋白H3的磷酸化和乙酰化,具体是通过IKKα而非NF-κB DNA结合复合物。在行为上,我们发现抑制IKKα对染色质结构或NF-κB DNA结合复合物活性的调节会导致恐惧记忆重新巩固受损,并且在IKK被阻断的情况下,提高组蛋白乙酰化水平可挽救这种记忆缺陷。这些数据为海马体中IKK调节的转录机制提供了见解,这些机制是记忆重新巩固所必需的。