Memory Research Laboratory, Brain Institute, Federal University of Rio Grande do Norte, RN 59056-450 Natal, Brazil.
Memory Research Laboratory, Brain Institute, Federal University of Rio Grande do Norte, RN 59056-450 Natal, Brazil
J Neurosci. 2019 Mar 6;39(10):1828-1841. doi: 10.1523/JNEUROSCI.2270-18.2018. Epub 2019 Jan 8.
Object recognition memory (ORM) confers the ability to discriminate the familiarity of previously encountered items. Reconsolidation is the process by which reactivated memories become labile and susceptible to modifications. The hippocampus is specifically engaged in reconsolidation to integrate new information into the original ORM through a mechanism involving activation of brain-derived neurotrophic factor (BDNF) signaling and induction of LTP. It is known that BDNF can control LTP maintenance through protein kinase Mζ (PKMζ), an atypical protein kinase C isoform that is thought to sustain memory storage by modulating glutamatergic neurotransmission. However, the potential involvement of PKMζ in ORM reconsolidation has never been studied. Using a novel ORM task combined with pharmacological, biochemical, and electrophysiological tools, we found that hippocampal PKMζ is essential to update ORM through reconsolidation, but not to maintain the inactive recognition memory trace stored over time, in adult male Wistar rats. Our results also indicate that hippocampal PKMζ acts downstream of BDNF and controls AMPAR synaptic insertion to elicit reconsolidation and suggest that blocking PKMζ activity during this process deletes active ORM. Object recognition memory (ORM) is essential to remember facts and events. Reconsolidation integrates new information into ORM through changes in hippocampal plasticity and brain-derived neurotrophic factor (BDNF) signaling. In turn, BDNF enhances synaptic efficacy through protein kinase Mζ (PKMζ), which might preserve memory. Here, we present evidence that hippocampal PKMζ acts downstream of BDNF to regulate AMPAR recycling during ORM reconsolidation and show that this kinase is essential to update the reactivated recognition memory trace, but not to consolidate or maintain an inactive ORM. We also demonstrate that the amnesia provoked by disrupting ORM reconsolidation through PKMζ inhibition is due to memory erasure and not to retrieval failure.
对象识别记忆 (ORM) 使个体能够辨别先前遇到过的物品的熟悉程度。再巩固是指重新激活的记忆变得不稳定且易受影响的过程。海马体专门参与再巩固,通过涉及脑源性神经营养因子 (BDNF) 信号的激活和长时程增强 (LTP) 的诱导,将新信息整合到原始 ORM 中。已知 BDNF 可以通过蛋白激酶 Mζ (PKMζ) 控制 LTP 的维持,PKMζ 是一种非典型蛋白激酶 C 同工型,被认为通过调节谷氨酸能神经传递来维持记忆存储。然而,PKMζ 参与 ORM 再巩固的潜在作用从未被研究过。使用一种新的 ORM 任务,结合药理学、生物化学和电生理学工具,我们发现海马体中的 PKMζ 对于通过再巩固更新 ORM 是必不可少的,但对于维持随时间推移而存储的非活动识别记忆痕迹则不是必需的,在成年雄性 Wistar 大鼠中。我们的结果还表明,海马体中的 PKMζ 作用于 BDNF 的下游,控制 AMPAR 突触插入以引发再巩固,并表明在此过程中阻断 PKMζ 活性会删除活跃的 ORM。对象识别记忆 (ORM) 对于记住事实和事件至关重要。再巩固通过海马体可塑性和脑源性神经营养因子 (BDNF) 信号的变化将新信息整合到 ORM 中。反过来,BDNF 通过蛋白激酶 Mζ (PKMζ) 增强突触效能,这可能有助于记忆的保存。在这里,我们提供的证据表明,海马体中的 PKMζ 作用于 BDNF 的下游,以调节 ORM 再巩固过程中的 AMPAR 循环,表明这种激酶对于更新重新激活的识别记忆痕迹是必不可少的,但对于巩固或维持非活动的 ORM 则不是必需的。我们还证明,通过 PKMζ 抑制破坏 ORM 再巩固引起的健忘症是由于记忆擦除而不是检索失败。