Li H Y, Dai L J, Krieger C, Quamme G A
Department of Medicine, University of British Columbia, University Hospital, Vancouver, Canada.
Biochim Biophys Acta. 1993 Jun 19;1181(3):307-15. doi: 10.1016/0925-4439(93)90037-2.
Intracellular magnesium is associated with intracellular ATP concentrations as Mg-ATP2- and is involved with many enzymes in energy utilization. Intracellular Mg2+ has also been postulated to be involved with various Ca2+ actions. We determined adenine nucleotide concentrations (ATP, ADP and AMP) by HPLC and the associated changes in intracellular free Mg2+ ([Mg2+]i) by fluorescent methods in an epithelial cell line (opossum kidney cells). CCCP (a mitochondrial uncoupler), iodoacetate and amobarbital resulted in marked and rapid falls in [ATP]i with disproportionate increases in [Mg2+]i. These studies indicate that we are able to distinguish Mg2+ movements from Ca2+ by fluorescent techniques and suggests that intracellular regulation of [Mg2+]i is distinctive from those of [Ca2+]i. As CCCP plus amobarbital are reversible, we removed these inhibitors and tested the effect of Mg(2+)-availability on ATP depletion and recovery. The response of magnesium-depleted cells (basal [Mg2+]i 231 +/- 10 microM) following inhibitor-induced energy depletion and ATP recovery were similar to control cells. Accordingly, intracellular [Mg2+]i does not appear to be a limiting factor in ATP regeneration following removal of the chemical hypoxic insult. Finally, exogenous application of Na2ATP2- altered intracellular energy levels in normal and energy depleted cells but was without effect on [Mg2+]i. These studies suggest that intracellular ATP levels do not directly alter intracellular [Mg2+]i control and, in turn, intracellular free Mg2+ is not a limiting factor in ATP regeneration following energy depletion with chemical hypoxia.
细胞内镁与细胞内ATP浓度相关,以Mg-ATP2-的形式存在,并参与能量利用中的多种酶促反应。细胞内Mg2+也被认为与各种Ca2+作用有关。我们通过高效液相色谱法测定腺嘌呤核苷酸浓度(ATP、ADP和AMP),并通过荧光法测定上皮细胞系(负鼠肾细胞)中细胞内游离Mg2+([Mg2+]i)的相关变化。羰基氰化物间氯苯腙(CCCP,一种线粒体解偶联剂)、碘乙酸盐和异戊巴比妥导致[ATP]i显著快速下降,而[Mg2+]i不成比例地增加。这些研究表明,我们能够通过荧光技术区分Mg2+和Ca2+的移动,并表明细胞内[Mg2+]i的调节与[Ca2+]i的调节不同。由于CCCP加异戊巴比妥是可逆的,我们去除这些抑制剂,并测试了Mg2+可用性对ATP消耗和恢复的影响。抑制剂诱导能量消耗和ATP恢复后,镁缺乏细胞(基础[Mg2+]i为231±10μM)的反应与对照细胞相似。因此,在去除化学性缺氧损伤后,细胞内[Mg2+]i似乎不是ATP再生的限制因素。最后,外源性应用Na2ATP2-改变了正常细胞和能量耗尽细胞的细胞内能量水平,但对[Mg2+]i没有影响。这些研究表明,细胞内ATP水平不会直接改变细胞内[Mg2+]i的控制,反过来,细胞内游离Mg2+也不是化学性缺氧导致能量耗尽后ATP再生的限制因素。