研究进展, 更新时间: 2005年8月17日
  由美国生科集团 (BVTech, Inc.) 主办
  
脂蛋白受体Apoer2的特异结合介入Reelin对突触可塑性和记忆的调节
2005-8-17
  

学习与记忆由多种机制调节。本文表明, Apoer2 与NMDA受体形成功能性复合体, 它的配体Reelin通过Apoer2显著性提高长时程增强效应 (LTP)。小鼠缺失Apoer2, 学习与记忆能力下降。本研究为学习与记忆的解释提供一个新机制。


Modulation of synaptic plasticity and memory by reelin involves differential splicing of the lipoprotein receptor apoer2.

Beffert U, Weeber EJ, Durudas A, Qiu S, Masiulis I, Sweatt JD, Li WP, Adelmann G, Frotscher M, Hammer RE, Herz J.

Apolipoprotein E receptor 2 (Apoer2), a member of the LDL receptor gene family, and its ligand Reelin control neuronal migration during brain development. Apoer2 is also essential for induction of long-term potentiation (LTP) in the adult brain. Here we show that Apoer2 is present in the postsynaptic densities of excitatory synapses where it forms a functional complex with NMDA receptors. Reelin signaling through Apoer2 markedly enhances LTP through a mechanism that requires the presence of amino acids encoded by an exon in the intracellular domain of Apoer2. This exon is alternatively spliced in an activity-dependent manner and is required for Reelin-induced tyrosine phosphorylation of NMDA receptor subunits. Mice constitutively lacking the exon perform poorly in learning and memory tasks. Thus, alternative splicing of Apoer2, a novel component of the NMDA receptor complex, controls the modulation of NMDA receptor activity, synaptic neurotransmission, and memory by Reelin.

Source: Neuron. 2005 Aug 18; 47(4):567-79
 

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