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首页> 外文期刊>Neuron >Bidirectional regulation of dendritic voltage-gated potassium channels by the fragile X mental retardation protein.
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Bidirectional regulation of dendritic voltage-gated potassium channels by the fragile X mental retardation protein.

机译:脆性X智力低下蛋白对树突状电压门控钾通道的双向调节。

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How transmitter receptors modulate neuronal signaling by regulating voltage-gated ion channel expression remains an open question. Here we report dendritic localization of mRNA of Kv4.2 voltage-gated potassium channel, which regulates synaptic plasticity, and its local translational regulation by fragile X mental retardation protein (FMRP) linked to fragile X syndrome (FXS), the most common heritable mental retardation. FMRP suppression of Kv4.2 is revealed by elevation of Kv4.2 in neurons from fmr1 knockout (KO) mice and in neurons expressing Kv4.2-3'UTR that binds FMRP. Moreover, treating hippocampal slices from fmr1 KO mice with Kv4 channel blocker restores long-term potentiation induced by moderate stimuli. Surprisingly, recovery of Kv4.2 after N-methyl-D-aspartate receptor (NMDAR)-induced degradation also requires FMRP, likely due to NMDAR-induced FMRP dephosphorylation, which turns off FMRP suppression of Kv4.2. Our study of FMRP regulation of Kv4.2 deepens our knowledge of NMDAR signaling and reveals a FMRP target of potential relevance to FXS.
机译:递质受体如何通过调节电压门控离子通道表达来调节神经元信号仍然是一个悬而未决的问题。在这里,我们报告了Kv4.2电压门控钾通道的mRNA的树突状定位,它调节突触可塑性,并通过与脆性X综合征(FXS)(最常见的遗传性精神病)相关的脆性X智力低下蛋白(FMRP)对其局部翻译进行调控。迟钝。在来自fmr1基因敲除(KO)小鼠的神经元中和表达与FMRP结合的Kv4.2-3'UTR的神经元中,Kv4.2的升高揭示了FMRP对Kv4.2的抑制。此外,用Kv4通道阻滞剂处理fmr1 KO小鼠的海马切片可恢复中度刺激诱导的长期增强作用。出人意料的是,N-甲基-D-天冬氨酸受体(NMDAR)诱导的降解后恢复Kv4.2也需要FMRP,这可能是由于NMDAR诱导的FMRP脱磷酸作用,从而关闭了FMRP对Kv4.2的抑制。我们对Kv4.2的FMRP调节的研究加深了我们对NMDAR信号的了解,并揭示了与FXS潜在相关的FMRP目标。

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