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Different transporter systems regulate extracellular GABA from vesicular and non-vesicular sources

机译:不同的转运系统调节水泡和非水泡来源的细胞外GABA

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摘要

Tonic GABA type A (GABAA) conductance is a key factor regulating neuronal excitability and computation in neuronal networks. The magnitude of the tonic GABAA conductance depends on the concentration of ambient GABA originating from vesicular and non-vesicular sources and is tightly regulated by GABA uptake. Here we show that the transport system regulating ambient GABA responsible for tonic GABAA conductances in hippocampal CA1 interneurons depends on its source. In mice, GABA from vesicular sources is regulated by mouse GABA transporter 1 (mGAT1), while that from non-vesicular sources by mouse GABA transporters 3/4 (mGAT3/4). This finding suggests that the two transporter systems do not just provide backup for each other, but regulate distinct signaling pathways. This allows individual tuning of the two signaling systems and indicates that drugs designed to act at specific transporters will have distinct therapeutic actions.
机译:进补GABA A型(GABAA)电导是调节神经元网络中神经元兴奋性和计算能力的关键因素。滋补GABAA电导的大小取决于源自囊泡和非囊泡来源的周围GABA的浓度,并受GABA吸收的严格调节。在这里,我们显示调节海马CA1 interneurons的滋补GABAA电导的环境GABA的运输系统取决于其来源。在小鼠中,水泡来源的GABA受小鼠GABA转运蛋白1(mGAT1)的调节,而非水泡来源的GABA受小鼠GABA转运蛋白3/4(mGAT3 / 4)的调节。这一发现表明,这两个转运系统不仅为彼此提供了后备,而且还调节了不同的信号通路。这允许分别调节两个信号系统,并表明设计用于特定转运蛋白的药物将具有独特的治疗作用。

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