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Patterned expression of ion channel genes in mouse dorsal raphe nucleus determined with the Allen Mouse Brain Atlas

机译:艾伦小鼠脑图谱确定小鼠背缝核中离子通道基因的模式表达

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The dorsal raphe nucleus (DR) is the major source of serotonin (5-hydroxytryptamine, 5-HT) in the forebrain and dysfunction of this midbrain structure is implicated in affective disorders. The DR is composed of several types of 5-HT and non-5-HT neurons and their excitable-membrane properties are heterogeneous and overlapping. In order to understand how these properties may be generated, we examined the mRNA expression patterns of voltage- and ligand-gated ion channels in the DR using the Allen Mouse Brain Atlas. Since DR cytoarchitecture is organized with respect to the midline, we sought to identify genes that were expressed in a pattern with respect to the midline, either enriched or depleted, rather than those that were homogenously expressed throughout the DR. Less than 10% of the screened genes for voltage-gated ion channels showed patterned expression within the DR. Identified genes included voltage-gated sodium channel beta subunits, potassium channels, P/Q-, N-type calcium channels, as well as the alpha2/delta-1 calcium channel. Several voltage-gated chloride channels were also identified, although these may function within intracellular compartments. Of the ligand-gated ion channels examined, 20% showed patterned expression. These consisted primarily of glutamate and GABA-A receptor subunits. The identified genes likely contribute to unique excitable properties of different groups of neurons in the DR and may include novel pharmacologic targets for affective disorders.
机译:背沟核(DR)是前脑中5-羟色胺(5-羟色胺,5-HT)的主要来源,这种中脑结构的功能障碍与情感障碍有关。 DR由几种类型的5-HT和非5-HT神经元组成,它们的兴奋膜特性是异质的和重叠的。为了理解如何产生这些特性,我们使用艾伦小鼠脑图谱检查了DR中电压和配体门控离子通道的mRNA表达模式。由于DR细胞结构是相对于中线组织的,因此我们试图鉴定相对于中线以富集或枯竭模式表达的基因,而不是在整个DR中均质表达的基因。电压门控离子通道的筛选基因中,只有不到10%的基因在DR中显示出模式表达。鉴定出的基因包括电压门控钠通道β亚基,钾通道,P / Q-,N型钙通道以及alpha2 / delta-1钙通道。还确定了几个电压门控氯离子通道,尽管这些通道可能在细胞内区室中起作用。在检查的配体门控离子通道中,有20%显示了模式表达。这些主要由谷氨酸和GABA-A受体亚基组成。鉴定出的基因可能有助于DR中不同组神经元的独特兴奋性,并且可能包括情感障碍的新药理学靶标。

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