Iida K, Shinki T, Yamaguchi A, DeLuca H F, Kurokawa K, Suda T
Department of Biochemistry, School of Dentistry, Showa University, Tokyo, Japan.
Proc Natl Acad Sci U S A. 1995 Jun 20;92(13):6112-6. doi: 10.1073/pnas.92.13.6112.
The vitamin D endocrine system is regulated reciprocally by renal 25-hydroxyvitamin D3 1 alpha- and 24-hydroxylases. Previously, we reported that renal proximal convoluted tubules, the major site of 1 alpha, 25-dihydroxyvitamin D3 production, have vitamin D receptors. In the presence of vitamin D receptors, renal proximal convoluted tubules cannot maintain the state of enhanced production of 1 alpha, 25-dihydroxyvitamin D3. To clarify this discrepancy, we proposed a working hypothesis for the reciprocal control of renal 25-hydroxyvitamin D3 1 alpha- and 24-hydroxylase activities. In rat models of enhanced renal production of 1 alpha, 25-dihydroxyvitamin D3, expression of vitamin D receptors and 25-hydroxyvitamin D3 24-hydroxylase mRNAs was strikingly suppressed in renal proximal convoluted tubules but not in the cortical collecting ducts. In vitamin D-deficient rats with up-regulated renal 25-hydroxyvitamin D3 1 alpha-hydroxylase activity, expression of vitamin D receptor mRNA in renal proximal convoluted tubules was also down-regulated, indicating that the down-regulation of vitamin D receptor mRNA is not the result of the enhanced production of 1 alpha, 25-dihydroxyvitamin D3. In Japanese quail models with up-regulated renal 25-hydroxyvitamin D3 1 alpha-hydroxylase activity by sex steroids, expression of vitamin D receptor mRNA was also down-regulated in the kidney but not in the duodenum. These results suggest that the down-regulation of vitamin D receptors plays a critical role in production of 1 alpha, 25-dihydroxyvitamin D3 in renal proximal convoluted tubules.
维生素D内分泌系统受肾脏25-羟基维生素D3 1α-羟化酶和24-羟化酶的相互调节。此前,我们报道过肾脏近端曲小管作为1α,25-二羟基维生素D3产生的主要部位,具有维生素D受体。在存在维生素D受体的情况下,肾脏近端曲小管无法维持1α,25-二羟基维生素D3增强产生的状态。为了阐明这一差异,我们提出了一个关于肾脏25-羟基维生素D3 1α-羟化酶和24-羟化酶活性相互控制的工作假说。在肾脏1α,25-二羟基维生素D3产生增强的大鼠模型中,肾脏近端曲小管中维生素D受体和25-羟基维生素D3 24-羟化酶mRNA的表达显著受到抑制,但在皮质集合管中未受抑制。在肾脏25-羟基维生素D3 1α-羟化酶活性上调的维生素D缺乏大鼠中,肾脏近端曲小管中维生素D受体mRNA的表达也下调,这表明维生素D受体mRNA的下调不是1α,25-二羟基维生素D3产生增强的结果。在性类固醇使肾脏25-羟基维生素D3 1α-羟化酶活性上调的日本鹌鹑模型中,肾脏中维生素D受体mRNA的表达也下调,但十二指肠中未下调。这些结果表明,维生素D受体的下调在肾脏近端曲小管中1α,25-二羟基维生素D3的产生中起关键作用。