1,25-(OH)_2D_3对HL-60细胞具有促分化作用。本文报道了1,25-(OH)_2D_3在促进HL-60细胞分化前后胞液Ca~(2+)浓度、磷酸化酶a和微粒体Ca~(2+)-ATP酶活性的改变。结果表明,1,25-(OH)_2D_3加入HL-60细胞培养液后72小时,细胞NBT染色阳性率高于70%,形态向正常分化的细胞转化。同对,胞液Ca~(2+)浓度和微粒体Ca~(2+)-ATP酶活性明显降低,而磷酸化酶a活性显著升高。结果提示,在1,25-(OH)2_D_3作用下,HL-60细胞不仅杀菌功能增强,细胞内胞液Ca~(2+)浓度趋向正常,与钙恒稳有关的酶活性也同样发生改变。即1,25-(OH)_2D_3对HL-60细胞的诱导作用伴有钙恒稳的改变。这些变化与DMSO的作用相同。
Abstract
1,25-(OH)2D3 was reported to show the effects of inducing differentiation of HL-60 cells. In this work, the changes in concentration of cytosolic Ca2+,activity of cytosolic phosphorylase a and microsomal Ca2+-ATPase were determined, and the following results were obtained. After 72 h culture of HL-60 cells in the presence of 1,25-(OH)2D3, more than 70% of HL-60 cells showed positive reaction to NBT test indicating that differentiation of HL-60 cell was induced, The concentr- ation of cytosolic Ca2+ and the activity of microsomal Ca2+-ATPase was decreased obviously while the activity of phosphorylase a was increased remarkably.These results indicated that under the inducing effect of 1,25-(OH) 2D3 the bactericidal effect of HL-60 cells was strenthened, the concentration of cytosolic Ca 2+ tended to normal level and the activity of enzymes concerning with Ca2+ homeostasis were changed simultaneously. In other words, the inducing effect of 1,25-(OH)2D3 on HL-60 cells was accompanied by the changes of Ca2+ homeostasis. The same results were also found in cells under the inducing effect of DMSO.
关键词
HL-60细胞系 /
25-(OH)_2D_3 /
钙恒稳 /
Ca~(2+)-ATP酶 /
磷酸化酶a
{{custom_keyword}} /
{{custom_sec.title}}
{{custom_sec.title}}
{{custom_sec.content}}
参考文献
[1] Haussler M R, et al. New England J Med, 1977, 297:974-983
[2] Freake H C et al. Cancer Res, 1984, 44:3627-3631
[3] McCarthy D M et al. Leukemia Res, 1983, 7:51-55
[4] Tsuruo T et al. Cancer Chemother Pharmacol, 1985, 14:30-33
[5] Hait W N et al. Cancer Chemother Pharmacol, 1985, 14:202-205
[6] 王永才,等.血液骨髓细胞检查,北京:科学技术文献出版社,1989,335
[7] Tsien R Y et al. J Cell Biol, 1982, 94:325-334
[8] Chan K M et al. Anal Biochem, 1986, 157:375-380
[9] Lowry O H et al. J Biol Chem, 1951, 193:265-275
[10] Fiske C H et al. J Biol Chem, 1925, 66:375-400
[11] Criss W E. Fed Proc, 1982, 41:2289-2291
[12] Becker G L et al. J Biol Chem, 1980, 225:9009-9012
[13] Burgess G M et al. J Biol Chem, 1983, 258:15336-15345
[14] Bellomo G et al. FEBS Letters, 1984, 168:38-42
[15] DiMonte D et al. Arch Biochem Biophys, 1984, 235:343-350
[16] Laporte D C et al. Biochem Biophys Res Commun, 1979, 86:1169-1177
{{custom_fnGroup.title_cn}}
脚注
{{custom_fn.content}}