Birge S J, Miller R
J Clin Invest. 1977 Nov;60(5):980-8. doi: 10.1172/JCI108878.
The response of chick intestine to vitamin D and its metabolites was studied in an organ culture preparation of chick ileum explants. Both 25-hydroxycholecalciferol (25-OHD(3)) at a concentration of 20 ng/ml or greater and 1,25-dihydroxycholecalciferol [1,25-(OH)(2)D(3)] at a concentration of 50 pg/ml or greater stimulated the rate of accumulation of [(32)P]phosphate and (45)Ca by the explants and the incorporation of [(3)H]thymidine into DNA. The accumulation of [(32)P]phosphate by the explants was against a concentration gradient and inhibited by ouabain and dinitrophenol. Two saturable mechanisms appeared to mediate the cellular accumulation of phosphate with K(a) of 0.0047 and 0.125 mM, respectively. The V(max) of the lower affinity transport mechanism was accelerated by 1,25-(OH)(2)D(3). Actinomycin D (5.0 mug/ml) did not block the intestinal response to 1,25-(OH)(2)D(3) stimulation of both [(32)p]phosphate and (45)Ca accumulation. Significant stimulation of [(32)P]phosphate accumulation was observed 30 min after the addition of 1,25-(OH)(2)D(3), preceding the sterol-induced increase in the rate of (45)Ca uptake by 30 min and the sterol-induced increase in [(3)H]thymidine incorporation into DNA by 150 min. Increasing extracellular phosphate concentration to 3.0 mM increased [(3)H]thymidine incorporation into DNA and the rate of (45)Ca uptake by the explants. Reducing extracellular phosphate concentration to 0.05 mM attenuated the response of the explants to 1,25-(OH)(2)D(3). From these observations it is postulated that the primary action of vitamin D sterols in the intestine is to enhance the ability of the mucosal cell to accumulate phosphate. The data suggest that restoration of intracellular phosphate levels may then permit expression of the cells' response to vitamin D sterols.
在鸡回肠外植体的器官培养制剂中研究了鸡肠道对维生素D及其代谢产物的反应。浓度为20 ng/ml或更高的25-羟基胆钙化醇(25-OHD(3))以及浓度为50 pg/ml或更高的1,25-二羟基胆钙化醇[1,25-(OH)(2)D(3)]均刺激外植体对[(32)P]磷酸盐和(45)Ca的积累速率以及[(3)H]胸苷掺入DNA的过程。外植体对[(32)P]磷酸盐的积累是逆浓度梯度进行的,并受到哇巴因和二硝基苯酚的抑制。似乎有两种可饱和机制介导细胞对磷酸盐的积累,其K(a)分别为0.0047和0.125 mM。较低亲和力转运机制的V(max)被1,25-(OH)(2)D(3)加速。放线菌素D(5.0 μg/ml)并未阻断肠道对1,25-(OH)(2)D(3)刺激[(32)p]磷酸盐和(45)Ca积累的反应。在添加1,25-(OH)(2)D(3)后30分钟观察到[(32)P]磷酸盐积累有显著刺激,比固醇诱导的(45)Ca摄取速率增加提前30分钟,比固醇诱导的[(3)H]胸苷掺入DNA增加提前150分钟。将细胞外磷酸盐浓度提高到3.0 mM会增加[(3)H]胸苷掺入DNA以及外植体对(45)Ca的摄取速率。将细胞外磷酸盐浓度降低到0.05 mM会减弱外植体对1,25-(OH)(2)D(3)的反应。根据这些观察结果推测,维生素D固醇在肠道中的主要作用是增强黏膜细胞积累磷酸盐的能力。数据表明,细胞内磷酸盐水平的恢复可能随后允许细胞表达对维生素D固醇的反应。