Chiba P, Wallner C, Kaiser E
Department of Medical Chemistry, University of Vienna, Austria.
Biochim Biophys Acta. 1988 Aug 19;971(1):38-45. doi: 10.1016/0167-4889(88)90159-0.
The effect of the cell cycle and differentiation on S-adenosylmethionine (SAM) metabolism in HL-60 cells has been investigated. Synthesis and pool sizes of SAM and S-adenosylhomocysteine (SAH) were cell-cycle-independent (SAM, 315 microM; SAH, 4.6 microM). The SAM-synthase (ATP: L-methionine S-adenosyltransferase) of HL-60 cells has a Km for methionine of 12.8 +/- 2.0 microM and thus appears to be of the intermediate Km type found in other malignant tissues. The enzyme does not show cell-cycle regulation. Treatment of cells with DMSO resulted in a rapid and marked decrease of SAM and SAH levels without affecting pool turnover or the SAM/SAH ratio. A decrease in SAM concentration could also be observed in a variant cell line resistant to differentiation with DMSO. DMSO inhibited SAM-synthase in cell-free extracts. This inhibition was noncompetitive with respect to L-methionine. Inhibition of SAM-synthase by cycloleucine lowered SAM levels in intact cells, but resulted in differentiation of only a minor percentage of cells. These data indicate that changes in SAM and SAH levels in HL-60 cells seem to be a consequence rather than a cause of differentiation.
研究了细胞周期和分化对HL-60细胞中S-腺苷甲硫氨酸(SAM)代谢的影响。SAM和S-腺苷同型半胱氨酸(SAH)的合成及池大小与细胞周期无关(SAM为315μM;SAH为4.6μM)。HL-60细胞的SAM合成酶(ATP:L-甲硫氨酸S-腺苷转移酶)对甲硫氨酸的Km值为12.8±2.0μM,因此似乎属于在其他恶性组织中发现的中间Km类型。该酶不显示细胞周期调控。用二甲基亚砜(DMSO)处理细胞导致SAM和SAH水平迅速且显著降低,而不影响池周转率或SAM/SAH比值。在对DMSO诱导分化有抗性的变异细胞系中也可观察到SAM浓度降低。DMSO抑制无细胞提取物中的SAM合成酶。这种抑制作用对L-甲硫氨酸而言是非竞争性的。环亮氨酸对SAM合成酶的抑制降低了完整细胞中的SAM水平,但仅导致一小部分细胞分化。这些数据表明,HL-60细胞中SAM和SAH水平的变化似乎是分化的结果而非原因。