Bikle D D, Murphy E W, Rasmussen H
J Clin Invest. 1975 Feb;55(2):299-304. doi: 10.1172/JCI107933.
Isolated kidney mitochondria prepared from Vitamin D-deficient chicks catalyze the conversion of 25-hydroxyvitamin D3 to 1,25 dihydroxyvitamin D3. It wasfound that changes in the concentrations of Ca-2plus, HPO4-2minus, and Hplus altered synthesis in an interrelated fashion. Increasing the Ca-2plus concentration from 10-6 to 10-5 M caused a four- to fivefold increase in 1 alpha-hydroxylase activity when the medium pH was between 6.5 and 7.0. increasing the [Ca2+] to 10-4 M caused to furhter stimulation. At higher pH values, Ca-2plus had little effect upon 1 alpha-hydroxylase activity. In the absence of calcium [Ca2+] less than or equal to 10-7 M), a change in pH from 6.5 to 7.1 had no effect upon 1 alpha-hydroxylase activity in the presence of 10-5 M calcium, increasing the medium pH had a biphasic effect. An increase in pH from 6.5 to 6.9 caused a 1.5-fold increase in 1 alpha-hydroxylase activity, but a further increase of the pH to 7.1 caused a profound decrease in rate of hydroxylation to approximately 20% of the peak value. Neither 10-5 M LaC13 nor 10 mug/ml of oligomycin altered the effects of Ca2+ upon hydroxylate activity. However, the effect of calcium was blocked by 2.5 times 10-5 M ruthenium red, 0.83 mug/ml of antimycin A, and 500 muM dinitrophenol. The clcium ionophore, A23187, decreased but did not prevent the stimulatory effect of calcium. These data are consistent with the concept that the [Ca2+ in the mitochondrial matrix space is of importance in regulating the 1 alpha-hydroxylase. Phosphate exerted a biphasic effect on 1,25(OH)2D3 production with maximal stimulation (approximately twofold) at 1-3 mM. Calcium enhanced the stimulation by phosphate at all concentrations studied. The presence of potassium modified the interrelated effects of calcium and phosphate in two ways: 10-3 M calcium blocked the stimulation by phosphate; and in the presence of phosphate, 10-3 M calcium resulted in less 1,25(OH)2D3 production by production by isolated mitochondria are qualitatively similar to the effects of these ions on 1,25(OH)2D3 production yb isolated renal tubules.
从维生素D缺乏的雏鸡中分离出的肾线粒体可催化25-羟基维生素D3转化为1,25-二羟基维生素D3。研究发现,Ca2+、HPO42-和H+浓度的变化以相互关联的方式改变了合成过程。当培养基pH值在6.5至7.0之间时,将Ca2+浓度从10-6 M提高到10-5 M会使1α-羟化酶活性增加4至5倍。将[Ca2+]提高到10-4 M会导致进一步的刺激。在较高的pH值下,Ca2+对1α-羟化酶活性影响很小。在无钙([Ca2+]≤10-7 M)的情况下,在存在10-5 M钙的情况下,pH从6.5变为7.1对1α-羟化酶活性没有影响,提高培养基pH值有双相效应。pH从6.5增加到6.9会使1α-羟化酶活性增加1.5倍,但pH进一步增加到7.1会导致羟化速率大幅下降至峰值的约20%。10-5 M的LaC13和10 μg/ml的寡霉素均未改变Ca2+对羟化活性的影响。然而,2.5×10-5 M的钌红、0.83 μg/ml的抗霉素A和500 μM的二硝基苯酚可阻断钙的作用。钙离子载体A23187可降低但不能阻止钙的刺激作用。这些数据与线粒体基质空间中的[Ca2+]在调节1α-羟化酶方面很重要这一概念一致。磷酸盐对1,25(OH)2D3的产生有双相效应,在1-3 mM时刺激作用最大(约两倍)。在所有研究浓度下,钙均可增强磷酸盐的刺激作用。钾的存在以两种方式改变了钙和磷酸盐的相互关联效应:10-3 M的钙可阻断磷酸盐的刺激作用;在存在磷酸盐的情况下,10-3 M的钙导致分离的线粒体产生的1,25(OH)2D3减少。这些离子对分离的肾小管产生1,25(OH)2D3的影响在质量上与它们对分离的线粒体产生1,25(OH)2D3的影响相似。