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在已鉴定的5-羟色胺能神经元突触前终末处自抑制机制的特异性定位

Specific Localization of an Auto-inhibition Mechanism at Presynaptic Terminals of Identified Serotonergic Neurons.

作者信息

García-Ávila Miriam, Torres Ximena, Cercós Montserrat G, Trueta Citlali

机构信息

Departamento de Neurofisiología, Instituto Nacional de Psiquiatría Ramón de la Fuente Muñiz, Calzada México-Xochimilco 101, San Lorenzo Huipulco, Tlalpan 14370, Ciudad de México, Mexico.

出版信息

Neuroscience. 2021 Mar 15;458:120-132. doi: 10.1016/j.neuroscience.2020.12.015. Epub 2020 Dec 25.

Abstract

Auto-regulation mechanisms in serotonergic neurons regulate their electrical activity and secretion. Since these neurons release serotonin from different structural compartments - including presynaptic terminals, soma, axons and dendrites - through different mechanisms, autoregulation mechanisms are also likely to be different at each compartment. Here we show that a chloride-mediated auto-inhibitory mechanism is exclusively localized at presynaptic terminals, but not at extrasynaptic release sites, in serotonergic Retzius neurons of the leech. An auto-inhibition response was observed immediately after intracellular stimulation with an electrode placed in the soma, in neurons that were isolated and cultured retaining an axonal stump, where presynaptic terminals are formed near the soma, but not in somata isolated without axon, where no synaptic terminals are formed, nor in neurons in the nerve ganglion, where terminals are electrotonically distant from the soma. Furthermore, no auto-inhibition response was detected in either condition during the longer time course of somatic secretion. This shows that the auto-inhibition effects are unique to nerve terminals. We further determined that serotonin released from peri-synaptic dense-core vesicles contributes to auto-inhibition in the terminals, since blockade of L-type calcium channels, which are required to stimulate extrasynaptic but not synaptic release, decreased the amplitude of the auto-inhibition response. Our results show that the auto-regulation mechanism at presynaptic terminals is unique and different from that described in the soma of these neurons, further highlighting the differences in the mechanisms regulating serotonin release from different neuronal compartments, which expand the possibilities of a single neuron to perform multiple functions in the nervous system.

摘要

血清素能神经元中的自动调节机制调控着它们的电活动和分泌。由于这些神经元通过不同机制从不同结构区室——包括突触前终末、胞体、轴突和树突——释放血清素,自动调节机制在每个区室可能也有所不同。在这里,我们表明,氯化物介导的自动抑制机制仅局限于水蛭血清素能Retzius神经元的突触前终末,而非突触外释放位点。在用置于胞体的电极进行细胞内刺激后,立即在分离并培养的保留轴突残端的神经元中观察到自动抑制反应,在这些神经元中,突触前终末在胞体附近形成,但在没有轴突的分离胞体中未观察到自动抑制反应,因为在这些胞体中没有形成突触终末,在神经节中的神经元也未观察到自动抑制反应,因为在神经节中终末与胞体在电紧张上距离较远。此外,在胞体分泌的较长时间过程中,在两种情况下均未检测到自动抑制反应。这表明自动抑制作用是神经终末所特有的。我们进一步确定,从突触周围致密核心囊泡释放的血清素有助于终末中的自动抑制,因为阻断L型钙通道(刺激突触外而非突触释放所必需的通道)会降低自动抑制反应的幅度。我们的结果表明,突触前终末的自动调节机制是独特的,与这些神经元胞体中所描述的机制不同,这进一步突出了调节血清素从不同神经元区室释放的机制差异,这些差异扩展了单个神经元在神经系统中执行多种功能的可能性。

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