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首页> 外文期刊>The Journal of Comparative Neurology >Localization of the mouse alpha1A-adrenergic receptor (AR) in the brain: alpha1AAR is expressed in neurons, GABAergic interneurons, and NG2 oligodendrocyte progenitors.
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Localization of the mouse alpha1A-adrenergic receptor (AR) in the brain: alpha1AAR is expressed in neurons, GABAergic interneurons, and NG2 oligodendrocyte progenitors.

机译:小鼠alpha1A-肾上腺素能受体(AR)在大脑中的定位:alpha1AAR在神经元,GABA能中间神经元和NG2少突胶质祖细胞中表达。

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alpha(1)-Adrenergic receptors (ARs) are not well defined in the central nervous system. The particular cell types and areas that express these receptors are uncertain because of the lack of high avidity antibodies and selective ligands. We have developed transgenic mice that either systemically overexpress the human alpha(1A)-AR subtype fused with the enhanced green fluorescent protein (EGFP) or express the EGFP protein alone under the control of the mouse alpha(1A)-AR promoter. We confirm our transgenic model against the alpha(1A)-AR knockout mouse, which expresses the LacZ gene in place of the coding region for the alpha(1A)-AR. By using these models, we have now determined cellular localization of the alpha(1A)-AR in the brain, at the protein level. The alpha(1A)-AR or the EGFP protein is expressed prominently in neuronal cells in the cerebral cortex, hippocampus, hypothalamus, midbrain, pontine olivary nuclei, trigeminal nuclei, cerebellum, and spinal cord. The types of neurons were diverse, and the alpha(1A)-AR colocalized with markers for glutamic acid decarboxylase (GAD), gamma-aminobutyric acid (GABA), and N-methyl-D-aspartate (NMDA) receptors. Recordings from alpha(1A)-AR EGFP-expressing cells in the stratum oriens of the hippocampal CA1 region confirmed that these cells were interneurons. We could not detect expression of the alpha(1A)-AR in mature astrocytes, oligodendrocytes, or cerebral blood vessels, but we could detect the alpha(1A)-AR in oligodendrocyte progenitors. We conclude that the alpha(1A)-AR is abundant in the brain, expressed in various types of neurons, and may regulate the function of oligodendrocyte progenitors, interneurons, GABA, and NMDA receptor containing neurons.
机译:α(1)-肾上腺素能受体(ARs)在中枢神经系统中的定义不明确。由于缺乏高亲和力抗体和选择性配体,表达这些受体的特定细胞类型和区域尚不确定。我们已经开发了转基因小鼠,可以全身性地过量表达与增强型绿色荧光蛋白(EGFP)融合的人alpha(1A)-AR亚型,或在小鼠alpha(1A)-AR启动子的控制下单独表达EGFP蛋白。我们确认了针对alpha(1A)-AR基因敲除小鼠的转基因模型,该小鼠表达LacZ基因代替了alpha(1A)-AR的编码区。通过使用这些模型,我们现在确定了在蛋白质水平上大脑中α(1A)-AR的细胞定位。 alpha(1A)-AR或EGFP蛋白在大脑皮层,海马,下丘脑,中脑,桥脑橄榄核,三叉神经核,小脑和脊髓的神经元细胞中显着表达。神经元的类型是多种多样的,并且alpha(1A)-AR与谷氨酸脱羧酶(GAD),γ-氨基丁酸(GABA)和N-甲基-D-天冬氨酸(NMDA)受体的标记共定位。海马CA1区原始层中表达alpha(1A)-AR EGFP的细胞的记录证实这些细胞是中间神经元。我们无法在成熟的星形胶质细胞,少突胶质细胞或脑血管中检测到alpha(1A)-AR的表达,但是我们可以检测到少突胶质细胞祖细胞中的alpha(1A)-AR。我们得出的结论是,alpha(1A)-AR在大脑中丰富,在各种类型的神经元中表达,并且可能调节少突胶质细胞祖细胞,中间神经元,GABA和包含NMDA受体的神经元的功能。

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