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首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Mitochondrial permeability transition and calcium dynamics in striatal neurons upon intense NMDA receptor activation.
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Mitochondrial permeability transition and calcium dynamics in striatal neurons upon intense NMDA receptor activation.

机译:强烈的NMDA受体激活后,纹状体神经元中的线粒体通透性转变和钙动力学。

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摘要

Deregulation of the intracellular Ca2+ homeostasis by NMDA receptor activation leads to neuronal cell death. Induction of the mitochondrial permeability transition pore (MPT) by Ca2+ is a critical event in mediating cell death. In this study, we used fluorescent Ca2+ indicators to investigate the effect of high concentrations of NMDA on cytosolic and mitochondrial Ca2+ concentrations ([Ca2+]c and [Ca2+]m, respectively) in cultured striatal neurons. Exposure to NMDA resulted in an immediate, sustained increase in [Ca2+]c followed by a secondary increase in [Ca2+]c. This second increase of [Ca2+]c was prevented by pretreatment with N-methyl-valine-4-cyclosporin (NMV-Cys). Exposure of neurons to NMDA also resulted in an increase in [Ca2+]m that was followed by a precipitous decrease in the rhod-2 signal. This decrease followed the time frame of the secondary increase in [Ca2+]c. Preincubation of the neurons with NMV-Cys prevented the decrease in rhod-2 fluorescence. These dynamic changes in the rhod-2 signal and [Ca2+]m in response to NMDA were confirmed by using confocal microscopy. The presented results indicate that MPT can be detected in living neurons using fluorescent Ca2+ indicators, which would allow the study of the physiological role of MPT in cell death.
机译:NMDA受体激活使细胞内Ca2 +稳态失调导致神经元细胞死亡。 Ca2 +诱导线粒体通透性过渡孔(MPT)是介导细胞死亡的关键事件。在这项研究中,我们使用荧光Ca2 +指标来研究高浓度NMDA对培养的纹状体神经元中胞质和线粒体Ca2 +浓度(分别为[Ca2 +] c和[Ca2 +] m)的影响。暴露于NMDA会导致[Ca2 +] c立即持续增加,随后[Ca2 +] c出现二次增加。通过用N-甲基-缬氨酸-4-环孢菌素(NMV-Cys)预处理可以防止[Ca2 +] c的第二增加。神经元暴露于NMDA也会导致[Ca2 +] m的增加,然后是rhod-2信号的急剧下降。该下降遵循[Ca2 +] c二次上升的时间范围。用NMV-Cys对神经元进行预温育可防止rhod-2荧光减少。通过使用共聚焦显微镜证实了rhod-2信号和[Ca2 +] m响应NMDA的动态变化。提出的结果表明,可以使用荧光Ca2 +指示剂在活神经元中检测MPT,这将有助于研究MPT在细胞死亡中的生理作用。

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