Kawahara Koichi, Sato Rie, Iwabuchi Sadahiro, Matsuyama Daisuke
Laboratory of Cellular Cybernetics, Graduate School of Information Science and Technology, Hokkaido University, Sapporo, Japan.
Chronobiol Int. 2008 Nov;25(6):868-81. doi: 10.1080/07420520802536387.
Magnesium ions (Mg(2+)) play a fundamental role in cellular function, but the cellular dynamic changes of intracellular Mg(2+) remain poorly delineated. The present study aims to clarify whether the concentration of intracellular Mg(2+) possibly changes cyclically in association with rhythmic contraction and intracellular Ca(2+) oscillation in cultured cardiac myocytes from neonatal rats. To do this, we performed a noise analysis of fluctuations in the concentration of intracellular Mg(2+) in cardiac myocytes. The concentration was estimated by loading cells with either Mg-fluo4/AM or KMG-20/AM. Results revealed that the intensity of Mg-fluo-4 or KMG-20 fluorescence fluctuated cyclically in association with the rhythmic contraction of cardiac myocytes. In addition, the simultaneous measurement of Fura2 and Mg-fluo-4 fluorescence revealed phase differences between the dynamics of the two signals, suggesting that the cyclic changes in the Mg-fluo-4 or KMG-20 fluorescent intensity actually reflected the changes in intracellular Mg(2+). The complete termination of spontaneous rhythmic contractions did not abolish Mg(2+) oscillations, suggesting that the rhythmic fluctuations in intracellular Mg(2+) did not result from mechanical movements. We suggest that the concentration of intracellular Mg(2+) changes cyclically in association with spontaneous, cyclic changes in the concentration of intracellular Ca(2+) of cardiac myocytes. A noise analysis of the fluctuation of subtle changes in fluorescence intensity could contribute to the elucidation of novel functional roles of Mg(2+) in cells.
镁离子(Mg(2+))在细胞功能中发挥着重要作用,但细胞内Mg(2+)的动态变化仍不清楚。本研究旨在阐明新生大鼠培养心肌细胞中细胞内Mg(2+)浓度是否可能与节律性收缩和细胞内Ca(2+)振荡相关联地周期性变化。为此,我们对心肌细胞内Mg(2+)浓度的波动进行了噪声分析。通过用Mg-fluo4/AM或KMG-20/AM加载细胞来估计浓度。结果显示,Mg-fluo-4或KMG-20荧光强度与心肌细胞的节律性收缩相关联地周期性波动。此外,同时测量Fura2和Mg-fluo-4荧光揭示了两个信号动态之间的相位差异,表明Mg-fluo-4或KMG-20荧光强度的周期性变化实际上反映了细胞内Mg(2+)的变化。自发节律性收缩的完全终止并未消除Mg(2+)振荡,表明细胞内Mg(2+)的节律性波动并非由机械运动引起。我们认为,细胞内Mg(2+)浓度与心肌细胞内细胞内Ca(2+)浓度的自发周期性变化相关联地周期性变化。对荧光强度细微变化波动的噪声分析可能有助于阐明Mg(2+)在细胞中的新功能作用。