Trechsel U, Bonjour J P, Fleisch H
J Clin Invest. 1979 Jul;64(1):206-17. doi: 10.1172/JCI109441.
A primary chick kidney cell culture is described, capable of forming 1,25-dihydroxyvitamin D3 [1,25(OH)2D3], 24,25-dihydroxyvitamin D3 [24,25(OH)2D3], and 1,24,25-trihydroxyvitamin D3 [1,24,25(OH)3D3] over several days. The apparent Km values were 0.125 microM for the 1-hydroxylase and 2.1 microM for the 24-hydroxylase. Exogenous 1,25(OH)2D3 decreased 1-hydroxylase and increased 24-hydroxylase within 4 h. 24,25(OH)2D3 produced similar effects, but only in the absence of fetal calf serum. R and S isomers of 1,24,25(OH)3D3 were about fives times less active than 1,25(OH)2D3. Bovine parathyroid hormone stimulated the 1- and reduced the 24-hydroxylase in 6 h, but this only occurred in cultures either previously treated with 1,25(OH)2D3 and EGTA to lower Ca to 0.8 mM or in cultures grown in the presence of 25-hydroxyvitamin D3 (25(OH)D3). Under the latter condition, the sensitivity to bovine parathyroid hormone was enhanced, 0.04 U/ml producing a maximum response. Synthetic aminoterminal tetratriacontapeptide (1-34) human parathyroid hormone was equally effective. In the absence of D metabolites, estradiol for 6 h produced a dose-dependent inhibition of the 1-hydroxylase, but no change in the 24-hydroxylase. Progesterone, testosterone, and corticosterone had no significant effect. In cultures grown in the presence of 25(OH)D3 no reproducible effects were obtained with either 1 microM estradiol or 1 microM testosterone, alone or in combination, but 5 microM corticosterone decreased the 1- and increased the 24-hydroxylase. Changes in Ca and P concentrations of the medium as well as addition of ethane-l-hydroxy-1, 1-diphosphate for 48 h did not affect any of the hydroxylase activities. The modulation of the hydroxylase activities by vitamin D3 metabolites and parathyroid hormone suggests that these factors regulate the renal hydroxylase by direct actions, whereas it would appear that ethane-1-hydroxy-1,1-diphosphate, Ca, P, and steroid may exert their influence indirectly.
本文描述了一种原代鸡肾细胞培养物,该培养物能够在数天内形成1,25 - 二羟基维生素D3 [1,25(OH)2D3]、24,25 - 二羟基维生素D3 [24,25(OH)2D3]和1,24,25 - 三羟基维生素D3 [1,24,25(OH)3D3]。1 - 羟化酶的表观Km值为0.125微摩尔,24 - 羟化酶的表观Km值为2.1微摩尔。外源性1,25(OH)2D3在4小时内降低1 - 羟化酶活性并增加24 - 羟化酶活性。24,25(OH)2D3产生类似作用,但仅在无胎牛血清时出现。1,24,25(OH)3D3的R和S异构体的活性比1,25(OH)2D3低约五倍。牛甲状旁腺激素在6小时内刺激1 - 羟化酶并降低24 - 羟化酶活性,但这仅发生在先前用1,25(OH)2D3和乙二醇双四乙酸处理以使钙浓度降至0.8毫摩尔/升的培养物中,或在25 - 羟基维生素D3 [25(OH)D3]存在下生长的培养物中。在后一种情况下,对牛甲状旁腺激素的敏感性增强,0.04单位/毫升产生最大反应。合成的氨基末端三十四肽(1 - 34)人甲状旁腺激素同样有效。在无维生素D代谢产物的情况下,雌二醇作用6小时对1 - 羟化酶产生剂量依赖性抑制,但对24 - 羟化酶无影响。孕酮、睾酮和皮质酮无显著作用。在25(OH)D3存在下生长的培养物中,单独或联合使用1微摩尔雌二醇或1微摩尔睾酮均未获得可重复的效应,但5微摩尔皮质酮降低1 - 羟化酶活性并增加24 - 羟化酶活性。培养基中钙和磷浓度的变化以及添加乙烷 - 1 - 羟基 - 1,1 - 二磷酸48小时均不影响任何羟化酶活性。维生素D3代谢产物和甲状旁腺激素对羟化酶活性的调节表明,这些因素通过直接作用调节肾羟化酶,而乙烷 - 1 - 羟基 - 1,1 - 二磷酸、钙、磷和类固醇似乎可能间接发挥其影响。