转译控制和自闭症样行为。

Cellular logistics Pub Date : 2013-01-01 Epub Date: 2013-04-04 DOI:10.4161/cl.24551
Christos G Gkogkas, Nahum Sonenberg
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引用次数: 21

摘要

自闭症谱系障碍(ASD)由一系列神经发育疾病组成,具有三个显著特征:社交互动减少、沟通障碍和重复/刻板行为。在最近的一项研究中,我们发现,由于Eif4ebp2 (eIF4E结合蛋白2)在小鼠体内的基因缺失,eIF4E(真核起始因子4E)依赖蛋白的合成增加,刺激神经素(Nlgns,突触细胞粘附分子,对突触调节很重要)的产生,并导致CA1锥体神经元兴奋性到抑制性突触传递(E/I)的不平衡。在Eif4ebp2-/-小鼠中,这种不平衡伴随着社会互动、沟通和重复/刻板行为的缺陷。我们使用一种化合物阻断帽依赖翻译,或者通过敲除Nlgn1,恢复了E/I平衡,逆转了自闭症样的社会缺陷。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Translational control and autism-like behaviors.

Translational control and autism-like behaviors.

AUTISM SPECTRUM DISORDERS (ASD) CONSIST OF A SPECTRUM OF NEURODEVELOPMENTAL DISEASES WITH THREE SALIENT FEATURES: reduced social interactions, impaired communication and repetitive/stereotyped behaviors. In a recent study we found that increased eIF4E (eukaryotic initiation factor 4E)-dependent protein synthesis as a result of genetic deletion of Eif4ebp2 (eIF4E-binding protein 2) in mice, stimulates the production of neuroligins (Nlgns, synaptic cell-adhesion molecules important for synapse regulation) and engenders an imbalance of excitatory to inhibitory synaptic transmission (E/I) in CA1 pyramidal neurons. This imbalance is accompanied with deficits in social interaction, communication and repetitive/stereotyped behaviors in Eif4ebp2-/- mice. Using a compound that blocks cap-dependent translation or by knocking down Nlgn1, we restored the E/I balance and reversed the autism-like social deficits.

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