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Excitotoxicity and ALS: What is unique about the AMPA receptors expressed on spinal motor neurons?

机译:兴奋性毒性和ALS:脊髓运动神经元上表达的AMPA受体有何独特之处?

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摘要

It has been repeatedly reported that spinal motor neurons are selectively vulnerable to AMPA receptor-mediated excitotoxicity. Therefore, identifying the uniqueness of AMPA receptors that are expressed on motor neurons, especially in individuals affected with sporadic amyotrophic lateral sclerosis (ALS) is essential for elucidating the etiology of this disorder. The mechanism that initiates motor neuronal death appears to be an exaggerated influx of Ca2+ through AMPA receptors. The determinants that affect this Ca2+ influx are Ca2+ permeability, which is regulated by the presence of the GluR2 subunit and by RNA editing at the Q/R site of GluR2; channel desensitization, which is regulated by alternative splicing at the flip/ flop site and by RNA editing at the R/G site of GluR subunits; and receptor density on the cell surface, which is controlled by many factors including regulatory proteins, direct phosphorylation and RNA editing at the Q/R site. This review focuses on recent progress on the molecular dynamics of AMPA receptors and discusses the pathophysiology of selective motor neuron death mediated by AMPA receptors in individuals affected with sporadic ALS.
机译:反复报道,脊髓运动神经元选择性地易受AMPA受体介导的兴奋性毒性作用。因此,鉴定在运动神经元上表达的AMPA受体的独特性,特别是在患有散发性肌萎缩性侧索硬化症(ALS)的个体中,对于阐明这种疾病的病因至关重要。启动运动神经元死亡的机制似乎是通过AMPA受体夸大的Ca2 +流入。影响Ca2 +流入的决定因素是Ca2 +通透性,其受GluR2亚基的存在和在GluR2 Q / R位点的RNA编辑调控。通道脱敏,其通过在触发器位点的选择性剪接和在GluR亚基的R / G位点处的RNA编辑来调节;细胞表面的受体密度,受许多因素控制,包括调节蛋白,直接磷酸化和Q / R位点的RNA编辑。这篇综述聚焦于AMPA受体分子动力学的最新进展,并讨论了由AMPA受体介导的散发性ALS患者个体选择性运动神经元死亡的病理生理。

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