Frankel T L, Mason R S, Hersey P, Murray E, Posen S
J Clin Endocrinol Metab. 1983 Sep;57(3):627-31. doi: 10.1210/jcem-57-3-627.
Two melanin-producing human melanoma cell lines originally established from fresh surgical specimens were incubated with 25 hydroxyvitamin D3 (25 OHD3). Both cell lines produced material comigrating with 1,25 dihydroxy-vitamin D3 (1,25(OH)2D3) and 24,25 dihydroxyvitamin D3 (24,25(OH)2D3) in straight and reverse phase high performance liquid chromatography systems and displacing the relevant labeled ligands in competitive binding assays. The material designated 1,25(OH)2D3 was found almost entirely within the cells, whereas 24,25(OH)2D3 was evenly distributed between cells and medium. The synthesis of dihydroxylated materials was time dependent and was not observed if the cells were boiled before incubation with 25 OHD3. Preincubation with 1,25(OH)2D3 caused an increase in the synthesis of 24,25(OH)2D3 and a decrease in the synthesis of 1,25(OH)2D3. Michaelis-Menten constant (Km) values were 1.4 X 10(-9) mol/liter 25 OHD3 for the 1-alpha-hydroxylase enzyme and 72 X 10(-9) mol/liter for 24-hydroxylase. These studies constitute further evidence for the extrarenal synthesis of 1,25(OH)2D3. The suppressibility of 1 alpha-hydroxylase by preincubation with 1,25(OH)2D3 suggests a regulatory function for this system in the skin.
最初从新鲜手术标本中建立的两个人黑色素瘤细胞系与25-羟基维生素D3(25-OHD3)一起孵育。在正相和反相高效液相色谱系统中,这两个细胞系均产生了与1,25-二羟基维生素D3(1,25(OH)2D3)和24,25-二羟基维生素D3(24,25(OH)2D3)共迁移的物质,并在竞争性结合试验中取代了相关的标记配体。被指定为1,25(OH)2D3的物质几乎完全存在于细胞内,而24,25(OH)2D3则均匀分布于细胞和培养基之间。二羟基化物质的合成是时间依赖性的,如果细胞在与25-OHD3孵育前煮沸则未观察到合成。用1,25(OH)2D3预孵育会导致24,25(OH)2D3的合成增加,而1,25(OH)2D3的合成减少。1-α-羟化酶的米氏常数(Km)值对于25-OHD3为1.4×10(-9)mol/升,对于24-羟化酶为72×10(-9)mol/升。这些研究为1,25(OH)2D3的肾外合成提供了进一步的证据。用1,25(OH)2D3预孵育对1-α-羟化酶的抑制作用表明该系统在皮肤中具有调节功能。