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海马体突触可塑性和空间记忆对整合素的需求。

Integrin requirement for hippocampal synaptic plasticity and spatial memory.

作者信息

Chan Chi-Shing, Weeber Edwin J, Kurup Sindhu, Sweatt J David, Davis Ronald L

机构信息

Department of Molecular and Cellular Biology, Division of Neuroscience, Baylor College of Medicine, Houston, Texas 77030, USA.

出版信息

J Neurosci. 2003 Aug 6;23(18):7107-16. doi: 10.1523/JNEUROSCI.23-18-07107.2003.

Abstract

The establishment of memory requires coordinated signaling between presynaptic and postsynaptic terminals in the CNS. The integrins make up a large family of cell adhesion receptors that are known to mediate bidirectional signaling between cells or between cells and their external environment. We show here that many different integrins, including alpha3 and alpha5, are expressed broadly in the adult mouse brain and are associated with synapses. Mice with genetically reduced expression of alpha3 integrin fail to maintain long-term potentiation (LTP) generated in hippocampal CA1 neurons. Mice with reduced expression of the alpha3 and alpha5 integrins exhibit a defect in paired-pulse facilitation. Mice with reduced expression of alpha3, alpha5, and alpha8 are defective in hippocampal LTP and spatial memory in the water maze but have normal fear conditioning. These results demonstrate that several different integrins are involved in physiological plasticity and provide the first evidence of their requirement for behavioral plasticity in vertebrates.

摘要

记忆的形成需要中枢神经系统中突触前和突触后终末之间的协同信号传递。整合素构成了一大类细胞黏附受体,已知其介导细胞之间或细胞与其外部环境之间的双向信号传递。我们在此表明,许多不同的整合素,包括α3和α5,在成年小鼠大脑中广泛表达并与突触相关。α3整合素基因表达降低的小鼠无法维持海马CA1神经元中产生的长时程增强(LTP)。α3和α5整合素表达降低的小鼠在双脉冲易化方面表现出缺陷。α3、α5和α8表达降低的小鼠在海马LTP和水迷宫空间记忆方面存在缺陷,但恐惧条件反射正常。这些结果表明,几种不同的整合素参与了生理可塑性,并为它们在脊椎动物行为可塑性中的需求提供了首个证据。

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