Safadi F F, Thornton P, Magiera H, Hollis B W, Gentile M, Haddad J G, Liebhaber S A, Cooke N E
Department of Medicine, University of Pennsylvania School of Medicine, Philadelphia 19104-6144, USA.
J Clin Invest. 1999 Jan;103(2):239-51. doi: 10.1172/JCI5244.
A line of mice deficient in vitamin D binding protein (DBP) was generated by targeted mutagenesis to establish a model for analysis of DBP's biological functions in vitamin D metabolism and action. On vitamin D-replete diets, DBP-/- mice had low levels of total serum vitamin D metabolites but were otherwise normal. When maintained on vitamin D-deficient diets for a brief period, the DBP-/-, but not DBP+/+, mice developed secondary hyperparathyroidism and the accompanying bone changes associated with vitamin D deficiency. DBP markedly prolonged the serum half-life of 25(OH)D and less dramatically prolonged the half-life of vitamin D by slowing its hepatic uptake and increasing the efficiency of its conversion to 25(OH)D in the liver. After an overload of vitamin D, DBP-/- mice were unexpectedly less susceptible to hypercalcemia and its toxic effects. Peak steady-state mRNA levels of the vitamin D-dependent calbindin-D9K gene were induced by 1,25(OH)2D more rapidly in the DBP-/- mice. Thus, the role of DBP is to maintain stable serum stores of vitamin D metabolites and modulate the rates of its bioavailability, activation, and end-organ responsiveness. These properties may have evolved to stabilize and maintain serum levels of vitamin D in environments with variable vitamin D availability.
通过靶向诱变产生了一组维生素D结合蛋白(DBP)缺陷的小鼠,以建立一个模型来分析DBP在维生素D代谢和作用中的生物学功能。在富含维生素D的饮食条件下,DBP基因敲除小鼠的血清维生素D代谢产物总量较低,但其他方面正常。当短期维持在维生素D缺乏的饮食条件下时,DBP基因敲除小鼠(而非野生型小鼠)出现了继发性甲状旁腺功能亢进以及与维生素D缺乏相关的伴随骨骼变化。DBP通过减缓肝脏对维生素D的摄取并提高其在肝脏中转化为25(OH)D的效率,显著延长了25(OH)D的血清半衰期,并略微延长了维生素D的半衰期。在维生素D过载后,DBP基因敲除小鼠出人意料地对高钙血症及其毒性作用更不敏感。在DBP基因敲除小鼠中,维生素D依赖性钙结合蛋白-D9K基因的峰值稳态mRNA水平被1,25(OH)2D诱导得更快。因此,DBP的作用是维持维生素D代谢产物的稳定血清储存,并调节其生物利用度、活化和终末器官反应性的速率。这些特性可能已经进化,以便在维生素D可利用性可变的环境中稳定和维持血清维生素D水平。