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首页> 外文期刊>Progress in brain research >'Synaptic tagging' and 'cross-tagging' and related associative reinforcement processes of functional plasticity as the cellular basis for memory formation.
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'Synaptic tagging' and 'cross-tagging' and related associative reinforcement processes of functional plasticity as the cellular basis for memory formation.

机译:“突触标记”和“交叉标记”以及相关的功能性可塑性增强过程,是记忆形成的细胞基础。

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摘要

We focus on new properties of cellular and network processes of memory formation involving 'synaptic tagging' and 'cross-tagging' during long-term potentiation (LTP) and long-term depression (LTD) as well as associative heterosynaptic interactions, the latter of which are characterized by a time-window of about 1h. About 20 years ago we showed for the first time that the maintenance of LTP, like memory storage, depends on intact protein synthesis and thus consists of at least two temporal phases. Later, similar properties for LTD were shown by our own and other laboratories. Here we describe the requirements for the induction of the transient early-LTP/LTD and of the protein synthesis-dependent late-LTP/LTD. Late-LTP/LTD depend on the associative activation of heterosynaptic inputs, i.e. the synergistic activation of glutamatergic and modulatory reinforcing inputs within specific, effective time-windows during their induction. The induction of late-LTP/LTD is characterized by novel, late-associative properties such as 'synaptic tagging', 'cross-tagging' and 'late-associative reinforcement'. All of these phenomena require the associative setting of synaptic tags as well as the availability of plasticity-related proteins (PRPs) and they are restricted to functional dendritic compartments, in general. 'Synaptic tagging' guarantees input specificity, 'cross-tagging' determines the interaction between LTP and LTD in a neuron, and thus both are required for the specific processing of afferent signals for the establishment of late-LTP/LTD. 'Late-associative reinforcement' describes a process where early-LTP/LTD by the co-activation of modulatory inputs can be transformed into late-LTP/LTD in activated synapses where a tag is set. Recent experiments in the freely moving rat revealed a number of modulatory brain structures involved in the transformation of early-plasticity events into long-lasting ones. Further to this, we have characterized time-windows and activation patterns to be effective in the reinforcement process. Studies using a combined electrophysiological and behavioural approach revealed the physiological relevance of these reinforcement processes, which is also supported by fMRI studies in humans, which led to the hypothesis outlined here on cellular and system memory-formation by late-associative heterosynaptic interactions at the cellular level during functional plasticity events.
机译:我们专注于记忆形成的细胞和网络过程的新特性,包括长期增强(LTP)和长期抑制(LTD)期间的“突触标记”和“交叉标记”,以及相关的异突触相互作用,后者其特点是时间窗约为1小时。大约20年前,我们首次证明LTP的维持(如记忆存储)取决于完整的蛋白质合成,因此至少由两个时间阶段组成。后来,我们自己的实验室和其他实验室也显示了LTD的类似属性。在这里,我们描述了诱导早期LTP / LTD和依赖蛋白质合成的晚期LTP / LTD的要求。 Late-LTP / LTD取决于异突触输入的相关激活,即在诱导过程中在特定的有效时间窗口内对谷氨酸能和调节性增强输入的协同激活。晚期LTP / LTD的诱导具有新颖的晚期缔合特性,例如“突触标记”,“交叉标记”和“晚期缔合增强”。所有这些现象都需要突触标签的关联设置以及可塑性相关蛋白(PRP)的可用性,并且通常将它们限制在功能性树突区室中。 “突触标记”保证输入的特异性,“交叉标记”确定神经元中LTP和LTD之间的相互作用,因此,对于后期LTP / LTD的建立,传入信号的特定处理都需要两者。 “后期联想强化”描述了一个过程,其中通过调制输入的共同激活将早期LTP / LTD转换为设置了标签的激活突触中的后期LTP / LTD。在可自由运动的大鼠中进行的最新实验表明,许多可调节的大脑结构参与了早期可塑性事件向持久性事件的转化。除此之外,我们还对时间窗和激活模式进行了表征,以在加固过程中发挥作用。使用组合的电生理学和行为学方法的研究揭示了这些增强过程的生理相关性,这也得到了人类功能磁共振成像研究的支持,这导致了此处概述的关于细胞和系统记忆形成的假说,是由细胞后期的关联性突触相互作用引起的。功能可塑性事件期间的水平。

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