White R E, Hartzell H C
Department of Anatomy and Cell Biology, Emory University School of Medicine, Atlanta, GA 30322.
Science. 1988 Feb 12;239(4841 Pt 1):778-80. doi: 10.1126/science.2448878.
Magnesium ions play a fundamental role in cellular function, but the effects of changes in the concentration of intracellular ionized magnesium ([Mg2+]i) on cell physiology have only recently received experimental attention. Increasing [Mg2+]i from 0.3 to 3.0 mM in cardiac cells by internal perfusion has only small effects on the basal voltage-gated calcium current (ICa) or on ICa elevated by dihydropyridine calcium channel agonists. In contrast, ICa elevated by cyclic adenosine monophosphate (cAMP)-dependent phosphorylation decreases by more than 50 percent. The effect of [Mg2+]i is not due to changes in the concentration of cAMP or in the velocity of phosphorylation but rather appears to be a direct effect on the phosphorylated channel or on channel dephosphorylation.
镁离子在细胞功能中发挥着重要作用,但细胞内游离镁离子浓度([Mg2+]i)变化对细胞生理学的影响直到最近才受到实验关注。通过内部灌注将心肌细胞中的[Mg2+]i从0.3 mM增加到3.0 mM,对基础电压门控钙电流(ICa)或二氢吡啶钙通道激动剂升高的ICa只有微小影响。相比之下,由环磷酸腺苷(cAMP)依赖性磷酸化升高的ICa降低超过50%。[Mg2+]i的作用不是由于cAMP浓度或磷酸化速度的变化,而是似乎对磷酸化通道或通道去磷酸化有直接影响。