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一种靶向跨同源 NCAM 结合位点的肽模拟物可促进海马体的空间学习和神经可塑性。

A peptide mimetic targeting trans-homophilic NCAM binding sites promotes spatial learning and neural plasticity in the hippocampus.

机构信息

Department of Life Sciences, The Open University, Milton Keynes, United Kingdom.

出版信息

PLoS One. 2011;6(8):e23433. doi: 10.1371/journal.pone.0023433. Epub 2011 Aug 24.

Abstract

The key roles played by the neural cell adhesion molecule (NCAM) in plasticity and cognition underscore this membrane protein as a relevant target to develop cognitive-enhancing drugs. However, NCAM is a structurally and functionally complex molecule with multiple domains engaged in a variety of actions, which raise the question as to which NCAM fragment should be targeted. Synthetic NCAM mimetic peptides that mimic NCAM sequences relevant to specific interactions allow identification of the most promising targets within NCAM. Recently, a decapeptide ligand of NCAM--plannexin, which mimics a homophilic trans-binding site in Ig2 and binds to Ig3--was developed as a tool for studying NCAM's trans-interactions. In this study, we investigated plannexin's ability to affect neural plasticity and memory formation. We found that plannexin facilitates neurite outgrowth in primary hippocampal neuronal cultures and improves spatial learning in rats, both under basal conditions and under conditions involving a deficit in a key plasticity-promoting posttranslational modification of NCAM, its polysialylation. We also found that plannexin enhances excitatory synaptic transmission in hippocampal area CA1, where it also increases the number of mushroom spines and the synaptic expression of the AMPAR subunits GluA1 and GluA2. Altogether, these findings provide compelling evidence that plannexin is an important facilitator of synaptic functional, structural and molecular plasticity in the hippocampal CA1 region, highlighting the fragment in NCAM's Ig3 module where plannexin binds as a novel target for the development of cognition-enhancing drugs.

摘要

神经细胞黏附分子(NCAM)在可塑性和认知中的关键作用突显了这种膜蛋白作为开发认知增强药物的相关靶点。然而,NCAM 是一种结构和功能复杂的分子,具有多个参与各种作用的结构域,这就提出了一个问题,即应该针对 NCAM 的哪个片段进行靶向。模拟与特定相互作用相关的 NCAM 序列的合成 NCAM 模拟肽允许确定 NCAM 内最有前途的靶标。最近,开发了一种 NCAM 的十肽配体——plannexin,它模拟了 Ig2 中的同种结合位点,并与 Ig3 结合——作为研究 NCAM 转相互作用的工具。在这项研究中,我们研究了 plannexin 影响神经可塑性和记忆形成的能力。我们发现 plannexin 促进原代海马神经元培养物中的神经突生长,并在基础条件和涉及 NCAM 的关键促进可塑性的翻译后修饰——其多聚唾液酸化缺失的条件下改善大鼠的空间学习。我们还发现 plannexin 增强了海马 CA1 区的兴奋性突触传递,在那里它还增加了蘑菇形棘突的数量和 AMPAR 亚基 GluA1 和 GluA2 的突触表达。总之,这些发现提供了令人信服的证据,表明 plannexin 是海马 CA1 区突触功能、结构和分子可塑性的重要促进剂,突出了 NCAM 的 Ig3 模块中 plannexin 结合的片段作为开发认知增强药物的新靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30be/3160849/7e8df8e6bcee/pone.0023433.g001.jpg

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