Suppr超能文献

树突突触部位蛋白质的局部合成:在突触可塑性和记忆巩固中的作用?

Local synthesis of proteins at synaptic sites on dendrites: role in synaptic plasticity and memory consolidation?

作者信息

Steward Oswald, Worley Paul

机构信息

Reeve-Irvine Research Center, Department of Anatomy/Neurobiology, College of Medicine, University of California at Irvine, 92697, USA.

出版信息

Neurobiol Learn Mem. 2002 Nov;78(3):508-27. doi: 10.1006/nlme.2002.4102.

Abstract

Long-lasting forms of memory are thought to be mediated by modifications in synapses that are induced by particular patterns of activity, take time to be established (consolidated), and involve new gene expression. The molecular mechanisms underlying such long-lasting synaptic modifications remain to be defined. Here, we focus on new findings regarding synapse-specific gene expression and especially the intracellular transport and synaptic targeting of the mRNA for a recently identified immediate early gene called activity-regulated cytoskeleton-associated protein (Arc). Arc mRNA is transported into dendrites after episodes of neuronal activation. The newly synthesized Arc mRNA localizes selectively at synapses that have experienced particular patterns of activity, and this targeting depends on NMDA receptor activation. Arc protein is assembled into the postsynaptic junction, and Arc expression is strongly induced by brief behavioral experiences in select populations of neurons. These features of Arc induction and trafficking reveal novel cellular mechanisms that are well suited to mediate long-term synapse-specific modifications. We will review findings from other laboratories that both LTP and memory are disrupted when Arc induction is blocked, and we will discuss the possibility that Arc protein may play a key role in activity-dependent synaptic modification.

摘要

持久形式的记忆被认为是由特定活动模式诱导的突触修饰介导的,这些修饰需要时间来建立(巩固),并涉及新的基因表达。这种持久突触修饰的分子机制仍有待确定。在这里,我们关注关于突触特异性基因表达的新发现,特别是一种最近鉴定出的立即早期基因——活性调节细胞骨架相关蛋白(Arc)的mRNA的细胞内运输和突触靶向。神经元激活后,Arc mRNA被转运到树突中。新合成的Arc mRNA选择性地定位于经历过特定活动模式的突触处,这种靶向依赖于NMDA受体激活。Arc蛋白组装到突触后连接中,并且在特定神经元群体中,短暂的行为经历会强烈诱导Arc表达。Arc诱导和运输的这些特征揭示了适合介导长期突触特异性修饰的新细胞机制。我们将回顾其他实验室的研究结果,即当Arc诱导被阻断时,长时程增强(LTP)和记忆都会受到破坏,并且我们将讨论Arc蛋白可能在活动依赖的突触修饰中起关键作用的可能性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验