牛嗜铬细胞胞内游离mg的定量和定位。

Liliana P Montezinho, Carla P Fonseca, Carlos F G C Geraldes, M Margarida C A Castro
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引用次数: 7

摘要

镁是所有生命系统的基本元素。细胞内游离Mg(2+)浓度([Mg(2+)](i))的定量是至关重要的,因为其基础值的变化可能是由于Mg(2+)代谢异常引起的不同病理的指示。在这项工作中,我们使用(31)P NMR和荧光光谱法测定了牛染色质细胞(一种神经元样细胞模型)中静止[Mg(2+)](i),并使用共聚焦激光扫描显微镜研究了这些细胞中游离Mg(2+)的空间分布。(31)在这种特殊情况下,由于这种细胞类型的一些特殊形态和生理特性,P核磁共振波谱法不能有效地测定[Mg(2+)](i)。使用荧光光谱和Mg(2+)敏感探针furaptra发现这些细胞的基础[Mg(2+)](i)值为0.551 +/- 0.008 mM;该值落在文献报道的不同来源神经元的浓度范围内。该技术是测定[Mg(2+)](i)的一种准确、灵敏的方法。用对Mg(2+)敏感的探针(Magnesium Green)共聚焦显微镜显示,核内游离的Mg(2+)似乎主要集中在核内及其周围。由于缺乏足够的空间分辨率,无法得出游离Mg(2+)在染色质颗粒和/或细胞质中的定位的任何结论,也无法探测区室化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Quantification and localization of intracellular free mg in bovine chromaffin cells.

Magnesium is an essential element for all living systems. The quantification of free intracellular Mg(2+) concentration ([Mg(2+)](i)) is of utmost importance since changes in its basal value may be an indication of different pathologies due to abnormalities of Mg(2+) metabolism. In this work we used (31)P NMR and fluorescence spectroscopy to determine the resting [Mg(2+)](i) in bovine chromaffin cells, a neuron-like cellular model, as well as confocal laser scanning microscopy to study the free Mg(2+) spatial distribution in these cells. (31)P NMR spectroscopy did not prove to be effective for the determination of [Mg(2+)](i) in this particular case due to some special morphological and physiological properties of this cell type. A basal [Mg(2+)](i) value of 0.551 +/- 0.008 mM was found for these cells using fluorescence spectroscopy and the Mg(2+)-sensitive probe furaptra; this value falls in the concentration range reported in the literature for neurons from different sources. This technique proved to be an accurate and sensitive tool to determine the [Mg(2+)](i).lntraceilular free Mg(2+) seems to be essentially localized in the nucleus and around it, as shown by confocal microscopy with the Mg(2+)-sensitive probe Magnesium Green. It was not possible to derive any conclusion about free Mg(2+) localization inside the chromaffin granules and/or in the cytoplasm due to the lack of sufficient spatial resolution and to probe compartmentalization.

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