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抑制性神经元AMPA受体的丧失导致了stargazer小鼠的共济失调和癫痫。

Loss of inhibitory neuron AMPA receptors contributes to ataxia and epilepsy in stargazer mice.

作者信息

Menuz Karen, Nicoll Roger A

机构信息

Departments of Cellular and Molecular Pharmacology and Physiology, University of California, San Francisco, San Francisco, California 94143. USA.

出版信息

J Neurosci. 2008 Oct 15;28(42):10599-603. doi: 10.1523/JNEUROSCI.2732-08.2008.

Abstract

Stargazer mice are characterized by ataxia and seizures, which resemble the human disorder absence epilepsy. Stargazin, the protein mutated in stargazer mice, promotes the expression and function of neuronal AMPA receptors (AMPARs). However, it is unclear how decreased expression of excitatory AMPARs generates stargazer seizures, given that seizures often result from increased neuronal excitability. Additionally, although stargazer ataxia has been attributed to loss of AMPARs from cerebellar granule cells, other cerebellar neurons have not been examined. To examine the role of AMPAR dysfunction in these behavioral phenotypes, electrophysiological recordings were used to probe AMPAR regulation in relevant brain regions. We found that both cerebellar Purkinje cells and inhibitory thalamic reticular nucleus neurons have strongly reduced synaptic AMPAR function in stargazer mice. Together, our data suggest that impaired AMPAR regulation in multiple neuron populations may contribute to the behavioral phenotypes of absence seizures and ataxia seen in stargazer mice and imply that an understanding of human genetic disorders will require knowledge of both the genes that are mutated as well as their precise cellular expression pattern.

摘要

“凝视者”小鼠的特征是共济失调和癫痫发作,这与人类失神癫痫疾病相似。“凝视者”小鼠中发生突变的蛋白质stargazin可促进神经元AMPA受体(AMPARs)的表达和功能。然而,鉴于癫痫发作通常是由神经元兴奋性增加引起的,目前尚不清楚兴奋性AMPARs表达降低是如何引发“凝视者”小鼠癫痫发作的。此外,尽管“凝视者”小鼠的共济失调被认为是由于小脑颗粒细胞中AMPARs缺失所致,但尚未对其他小脑神经元进行研究。为了研究AMPAR功能障碍在这些行为表型中的作用,我们使用电生理记录来探测相关脑区的AMPAR调节情况。我们发现,在“凝视者”小鼠中,小脑浦肯野细胞和抑制性丘脑网状核神经元的突触AMPAR功能均大幅降低。总之,我们的数据表明,多个神经元群体中AMPAR调节受损可能导致了“凝视者”小鼠出现失神癫痫发作和共济失调的行为表型,这意味着要理解人类遗传疾病,需要了解发生突变的基因及其精确的细胞表达模式。

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