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Stringent Specificity in the Construction of a GABAergic Presynaptic Inhibitory Circuit

机译:GABA能突触前抑制电路的构建中的严格特异性。

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摘要

GABAergic interneurons are key elements in neural coding, but the mechanisms that assemble inhibitory circuits remain unclear. In the spinal cord, the transfer of sensory signals to motor neurons is filtered by GABAergic interneurons that act presynaptically to inhibit sensory transmitter release and postsynaptically to inhibit motor neuron excitability. We show here that the connectivity and synaptic differentiation of GABAergic interneurons that mediate presynaptic inhibition is directed by their sensory targets. In the absence of sensory terminals these GABAergic neurons shun other available targets, fail to undergo presynaptic differentiation, and withdraw axons from the ventral spinal cord. A sensory-specific source of brain derived neurotrophic factor induces synaptic expression of the GABA synthetic enzyme GAD65 a defining biochemical feature of this set of interneurons. The organization of a GABAergic circuit that mediates presynaptic inhibition in the mammalian CNS is therefore controlled by a stringent program of sensory recognition and signaling.
机译:GABA能神经元是神经编码中的关键元素,但组装抑制回路的机制仍不清楚。在脊髓中,感觉信号向运动神经元的传递被GABA能神经元过滤,该神经元在神经突触前起到抑制感觉递质释放的作用,而在神经突触后则抑制运动神经元的兴奋性。我们在这里显示,介导突触前抑制的GABA能中间神经元的连通性和突触分化是由其感官目标指导的。在没有感觉末梢的情况下,这些GABA能神经元会避开其他可用靶标,无法进行突触前分化,并从腹侧脊髓撤出轴突。脑源性神经营养因子的感觉特异性来源诱导GABA合成酶GAD65的突触表达,这是这组中间神经元的生化特征。因此,通过严格的感觉识别和信号传递程序来控制在哺乳动物CNS中介导突触前抑制的GABA能回路的组织。

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