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基于记忆印迹受体镶嵌假说的分子基础。

On the molecular basis of the receptor mosaic hypothesis of the engram.

作者信息

Agnati Luigi F, Ferré Sergi, Leo Giuseppina, Lluis Carme, Canela Enric I, Franco Rafael, Fuxe Kjell

机构信息

Department of Biomedical Sciences, University of Modena, Modena, Italy.

出版信息

Cell Mol Neurobiol. 2004 Aug;24(4):501-16. doi: 10.1023/b:cemn.0000023626.35717.5d.

Abstract
  1. This paper revisits the so-called "receptor mosaic hypothesis" for memory trace formation in the light of recent findings in "functional (or interaction) proteomics." The receptor mosaic hypothesis maintains that receptors may form molecular aggregates at the plasma membrane level representing part of the computational molecular networks. 2. Specific interactions between receptors occur as a consequence of the pattern of transmitter release from the source neurons, which release the chemical code impinging on the receptor mosaics of the target neuron. Thus, the decoding of the chemical message depends on the receptors forming the receptor mosaics and on the type of interactions among receptors and other proteins in the molecular network with novel long-term mosaics formed by their stabilization via adapter proteins formed in target neurons through the incoming neurotransmitter code. The internalized receptor heteromeric complexes or parts of them may act as transcription factors for the formation of such adapter proteins. 3. Receptor mosaics are formed both at the pre- and postsynaptic level of the plasma membranes and this phenomenon can play a role in the Hebbian behavior of some synaptic contacts. The appropriate "matching" of the pre- with the postsynaptic receptor mosaic can be thought of as the "clamping of the synapse to the external teaching signal." According to our hypothesis the behavior of the molecular networks at plasma membrane level to which the receptor mosaics belong can be set in a "frozen" conformation (i.e. in a frozen functional state) and this may represent a mechanism to maintain constant the input to a neuron. 4. Thus, we are suggesting that molecular networks at plasma membrane level may display multiple "attractors" each of which stores the memory of a specific neurotransmitter code due to a unique firing pattern. Hence, this mechanism may play a role in learning processes where the input to a neuron is likely to remain constant for a while.
摘要
  1. 本文根据“功能(或相互作用)蛋白质组学”的最新研究成果,重新审视了关于记忆痕迹形成的所谓“受体镶嵌假说”。受体镶嵌假说认为,受体可能在质膜水平形成分子聚集体,这些聚集体代表了计算分子网络的一部分。2. 受体之间的特异性相互作用是源神经元释放递质模式的结果,源神经元释放化学编码,作用于靶神经元的受体镶嵌体。因此,化学信息的解码取决于形成受体镶嵌体的受体,以及受体与分子网络中其他蛋白质之间相互作用的类型,通过传入神经递质编码在靶神经元中形成衔接蛋白,使这些相互作用稳定下来,从而形成新的长期镶嵌体。内化的受体异聚体复合物或其部分可能作为形成此类衔接蛋白的转录因子。3. 受体镶嵌体在质膜的突触前和突触后水平均有形成,这种现象可能在某些突触联系的赫布行为中发挥作用。突触前与突触后受体镶嵌体的适当“匹配”可被视为“将突触钳制到外部教学信号”。根据我们的假说,受体镶嵌体所属的质膜水平分子网络的行为可以设置为“冻结”构象(即处于冻结的功能状态),这可能代表了一种使神经元输入保持恒定的机制。4. 因此,我们认为质膜水平的分子网络可能显示多个“吸引子”,每个吸引子由于独特的放电模式而存储特定神经递质编码的记忆。因此,这种机制可能在学习过程中发挥作用,在学习过程中,神经元的输入可能会在一段时间内保持恒定。

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