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组胺从培养的星形胶质细胞中引发谷氨酸释放。

Histamine elicits glutamate release from cultured astrocytes.

机构信息

Department of Pharmacology, Tohoku University Graduate School of Medicine, 2-1 Seiryo-machi, Aoba-ku, Sendai, 980-8575, Japan.

Department of Pharmacology, Tohoku University Graduate School of Medicine, 2-1 Seiryo-machi, Aoba-ku, Sendai, 980-8575, Japan.

出版信息

J Pharmacol Sci. 2018 Jun;137(2):122-128. doi: 10.1016/j.jphs.2018.05.002. Epub 2018 May 16.

DOI:10.1016/j.jphs.2018.05.002
PMID:29858014
Abstract

Astrocytes play key roles in regulating brain homeostasis and neuronal activity. This is, in part, accomplished by the ability of neurotransmitters in the synaptic cleft to bind astrocyte membrane receptors, activating signalling cascades that regulate concentration of intracellular Ca ([Ca]) and gliotransmitter release, including ATP and glutamate. Gliotransmitters contribute to dendrite formation and synaptic plasticity, and in some cases, exacerbate neurodegeneration. The neurotransmitter histamine participates in several physiological processes, such as the sleep-wake cycle and learning and memory. Previous studies have demonstrated the expression of histamine receptors on astrocytes, but until now, only a few studies have examined the effects of histamine on astrocyte intracellular signalling and gliotransmitter release. Here, we used the human astrocytoma cell line 1321N1 to study the role of histamine in astrocyte intracellular signalling and gliotransmitter release. We found that histamine activated astrocyte signalling through histamine H and H receptors, leading to distinct cellular responses. Activation of histamine H receptors caused concentration-dependent release of [Ca] from internal stores and concentration-dependent increase in glutamate release. Histamine H receptor activation increased cyclic adenosine monophosphate (cAMP) levels and phosphorylation of transcription factor cAMP response-element binding protein. Taken together, these data emphasize a role for histamine in neuron-glia communication.

摘要

星形胶质细胞在调节脑内稳态和神经元活动方面发挥着关键作用。这在一定程度上是通过神经递质在突触间隙中结合星形胶质细胞膜受体的能力来实现的,这种能力激活了信号级联反应,调节细胞内 Ca([Ca])浓度和神经递质的释放,包括 ATP 和谷氨酸。神经递质在树突形成和突触可塑性中发挥作用,在某些情况下会加剧神经退行性变。神经递质组胺参与了许多生理过程,如睡眠-觉醒周期、学习和记忆。以前的研究已经证明了组胺受体在星形胶质细胞上的表达,但到目前为止,只有少数研究检查了组胺对星形胶质细胞细胞内信号和神经递质释放的影响。在这里,我们使用人星形细胞瘤细胞系 1321N1 来研究组胺在星形胶质细胞细胞内信号和神经递质释放中的作用。我们发现,组胺通过组胺 H 和 H 受体激活星形胶质细胞信号,导致不同的细胞反应。组胺 H 受体的激活导致细胞内储存的 Ca([Ca])浓度依赖性释放和谷氨酸释放浓度依赖性增加。组胺 H 受体的激活增加了环磷酸腺苷(cAMP)水平和转录因子 cAMP 反应元件结合蛋白的磷酸化。总的来说,这些数据强调了组胺在神经元-胶质细胞通讯中的作用。

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