Di Francesco A, Desnoyer R W, Covacci V, Wolf F I, Romani A, Cittadini A, Bond M
Department of Anesthesia, Brigham and Womens' Hospital, Boston, Massachusetts, USA.
Arch Biochem Biophys. 1998 Dec 15;360(2):149-57. doi: 10.1006/abbi.1998.0937.
Magnesium (Mg) is required for cellular proliferation; however, the differences in subcellular regulation of Mg between proliferating and differentiated cells has not been determined. We used electron probe microanalysis (EPMA) to investigate the subcellular distribution of Mg in HL60 cells (a promyelocytic leukemia cell line) before and after retinoic acid (RA)-induced differentiation. Most intracellular Mg is bound to ATP and the Mg-ATP complex regulates several metabolic enzymes. We also compared alterations in Mg content following differentiation with the changes in ATP and ADP levels. Using atomic absorption spectrophotometry, we observed a significant decrease (-20%) in cellular Mg content in RA-differentiated HL60 cells. To investigate which intracellular compartments were involved in these changes, we analyzed subcellular elemental composition in freeze-dried cryosections of rapidly frozen undifferentiated and differentiated HL60 cells by EPMA. Following differentiation of HL60 cells, we observed an 18% decrease in Mg content in both the cytoplasm (regions of the cell excluding mitochondria and nuclei) and mitochondria. There was also a significant (40%) decrease in cytoplasmic Ca content after RA-induced differentiation. Nuclear Mg concentration was not significantly different between differentiated and undifferentiated HL60 cells, although differentiation was accompanied by a 30% decrease in the nuclear K/Na ratio. After differentiation, cellular ATP and ADP content decreased by 31 and 40%, respectively. We conclude that during exit from the cell cycle, Mg redistributes within cells and that the decrease in cytoplasmic and mitochondrial Mg is accompanied by a decrease in ATP and ADP content.
细胞增殖需要镁(Mg);然而,增殖细胞和分化细胞之间镁的亚细胞调节差异尚未确定。我们使用电子探针微分析(EPMA)来研究维甲酸(RA)诱导分化前后HL60细胞(一种早幼粒细胞白血病细胞系)中镁的亚细胞分布。大多数细胞内的镁与ATP结合,并且Mg-ATP复合物调节几种代谢酶。我们还将分化后镁含量的变化与ATP和ADP水平的变化进行了比较。使用原子吸收分光光度法,我们观察到RA分化的HL60细胞中细胞镁含量显著降低(-20%)。为了研究哪些细胞内区室参与了这些变化,我们通过EPMA分析了快速冷冻的未分化和分化的HL60细胞冻干冰冻切片中的亚细胞元素组成。HL60细胞分化后,我们观察到细胞质(细胞中不包括线粒体和细胞核的区域)和线粒体中的镁含量均下降了18%。RA诱导分化后细胞质钙含量也显著下降(40%)。分化和未分化的HL60细胞之间核镁浓度没有显著差异,尽管分化伴随着核K/Na比值下降30%。分化后,细胞ATP和ADP含量分别下降了31%和40%。我们得出结论,在细胞周期退出过程中,镁在细胞内重新分布,细胞质和线粒体中镁的减少伴随着ATP和ADP含量的减少。