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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Up- and down-regulation of Helix command-specific 2 (HCS2) gene expression in the nervous system of terrestrial snail Helix lucorum.
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Up- and down-regulation of Helix command-specific 2 (HCS2) gene expression in the nervous system of terrestrial snail Helix lucorum.

机译:陆地蜗牛Helico lucorum神经系统中Helix指令特异性2(HCS2)基因表达的上调和下调。

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摘要

A novel gene named Helix command-specific 2 (HCS2) was shown to be expressed predominantly in four giant parietal interneurons involved in withdrawal behavior of the terrestrial snail Helix lucorum L. and several single neurons in other ganglia. Decrease in spontaneous electrophysiological activity of neurons in the isolated CNS by 24h incubation in saline with elevated Mg(2+) concentration significantly decreased the number of HCS2-expressing neurons. Five short-term serotonin applications (each of 10microM), during a 24h incubation of the nervous system in saline induced expression of the HCS2 gene in many cells in cerebral, parietal, pleural and pedal ganglia. Dopamine applications under similar conditions were not effective. Application of anisomycin or cycloheximide, known to block protein synthesis, did not prevent the induction of HCS2 expression under serotonin influence. Skin injury elicited a significant increase in the number of HCS2-expressing cells 24h later in pleural and cerebral ganglia. Incubation of the isolated nervous system preparations for three days in culture medium elicited close to a maximum increase in number of HCS2-expressing cells. Elevation of the normal Mg(2+) concentration in the culture medium significantly decreased the number of cells demonstrating HCS2 expression. Application of the cAMP activator forskolin (10microM) increased the expression under Mg(2+), indicating that cAMP was involved in the up-regulation of HCS2. Application of thapsigargin (10microM), known to release Ca(2+) from intracellular stores, was also effective in increasing expression, suggesting participation of Ca(2+) in regulation of HCS2 expression. Cellular groups expressing the HCS2 gene under different conditions seem to be functionally related since it was demonstrated earlier that some neurons constituting these clusters are involved in the withdrawal behavior and the response of the organism to stress stimuli. From these results we suggest that the HCS2 pattern of expression can be down-regulated by a decrease in synaptic activity in the nervous system, and up-regulated by external noxious inputs, as well as the application of neurotransmitters and second messengers known to be involved in the withdrawal behavior and maintenance of isolated ganglia in culture medium. When up-regulated, the HCS2 expression appears, at least in part in neurons, to be involved in the withdrawal behavior.
机译:一个名为Helix Command-specific 2(HCS2)的新基因显示出主要在涉及地面蜗牛Helix lucorum L.和其他神经节中几个单个神经元的撤回行为的四个巨大顶顶神经元中表达。 Mg(2+)浓度升高的盐水中孵育24h,使分离的CNS中神经元的自发电生理活性降低,从而显着降低了表达HCS2的神经元的数量。在盐水中的神经系统孵育24小时期间,五次短期使用5-羟色胺(每次10μM)可诱导HCS2基因在脑,顶叶,胸膜和踏板神经节的许多细胞中表达。在类似条件下使用多巴胺无效。已知会阻断蛋白质合成的茴香霉素或环己酰亚胺的应用并不能阻止5-羟色胺影响下HCS2表达的诱导。皮肤损伤引起24小时后胸膜和脑神经节中表达HCS2的细胞数量显着增加。将分离的神经系统制剂在培养基中孵育三天,导致表达HCS2的细胞数量接近最大增加。培养基中正常Mg(2+)浓度的升高显着降低了显示HCS2表达的细胞数量。 cAMP激活剂福司高林(10microM)的应用增加了Mg(2+)下的表达,表明cAMP参与了HCS2的上调。 thapsigargin(10microM)的应用,已知会从细胞内存储中释放Ca(2+),在增加表达方面也很有效,表明Ca(2+)参与了HCS2表达的调节。在不同条件下表达HCS2基因的细胞群似乎在功能上相关,因为早先证明了构成这些簇的某些神经元参与了戒断行为和生物体对应激刺激的反应。根据这些结果,我们认为,可以通过神经系统中突触活性的降低来下调HCS2的表达模式,并通过外部有害输入以及已知涉及的神经递质和第二信使的应用来上调HCS2表达模式。在培养基中离体神经节的退缩行为和维持。当上调时,HCS2表达至少部分出现在神经元中,参与了戒断行为。

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