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θ刺激使海马体树突棘中的肌动蛋白聚合。

Theta stimulation polymerizes actin in dendritic spines of hippocampus.

作者信息

Lin Bin, Kramár Enikö A, Bi Xiaoning, Brucher Fernando A, Gall Christine M, Lynch Gary

机构信息

Department of Psychiatry and Human Behavior, University of California, Irvine, California 92617-1695, USA.

出版信息

J Neurosci. 2005 Feb 23;25(8):2062-9. doi: 10.1523/JNEUROSCI.4283-04.2005.

Abstract

It has been proposed that the endurance of long-term potentiation (LTP) depends on structural changes entailing reorganization of the spine actin cytoskeleton. The present study used a new technique involving intracellular and extracellular application of rhodamine-phalloidin to conventional hippocampal slices to test whether induction of LTP by naturalistic patterns of afferent activity selectively increases actin polymerization in juvenile to young adult spines. Rhodamine-phalloidin, which selectively binds to polymerized actin, was detected in perikarya and proximal dendrites of CA1 pyramidal cells that received low-frequency afferent activity but was essentially absent in spines and fine dendritic processes. Theta pattern stimulation induced LTP and caused a large (threefold), reliable increase in labeled spines and spine-like puncta in the proximal dendritic zone containing potentiated synapses. The spines frequently occurred in the absence of labeling to other structures but were also found in association with fluorescent dendritic processes. These effects were replicated (>10-fold increase in labeled spines) using extracellular applications of rhodamine-phalloidin. Increases in labeling appeared within 2 min, were completely blocked by treatments that prevent LTP induction, and occurred in slices prepared from young adult rats. These results indicate that near-threshold conditions for inducing stable potentiation cause the rapid polymerization of actin in mature spines and suggest that the effect is both sufficiently discrete to satisfy the synapse-specificity rule of LTP as well as rapid enough to participate in the initial stages of LTP consolidation.

摘要

有人提出,长期增强作用(LTP)的持续性取决于结构变化,这种变化需要对脊柱肌动蛋白细胞骨架进行重组。本研究使用了一种新技术,即将罗丹明 - 鬼笔环肽细胞内和细胞外应用于传统海马切片,以测试传入活动的自然模式诱导的LTP是否选择性地增加幼年到年轻成年脊柱中的肌动蛋白聚合。罗丹明 - 鬼笔环肽选择性地结合聚合的肌动蛋白,在接受低频传入活动的CA1锥体细胞的胞体和近端树突中被检测到,但在脊柱和细树突过程中基本不存在。θ模式刺激诱导了LTP,并导致在含有增强突触的近端树突区域中标记的脊柱和脊柱样小点大量(三倍)、可靠地增加。这些脊柱经常在没有标记到其他结构的情况下出现,但也与荧光树突过程相关联。使用罗丹明 - 鬼笔环肽的细胞外应用重复了这些效应(标记的脊柱增加了10倍以上)。标记增加在2分钟内出现,被阻止LTP诱导的处理完全阻断,并且发生在从年轻成年大鼠制备的切片中。这些结果表明,诱导稳定增强作用的近阈值条件会导致成熟脊柱中肌动蛋白的快速聚合,并表明这种效应既足够离散以满足LTP的突触特异性规则,又足够迅速以参与LTP巩固的初始阶段。

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