The vitamin D receptor in the proximal renal tubule is a key regulator of serum 1α,25-dihydroxyvitamin D3

被引:23
作者
Wang, Yongji [1 ,2 ]
Zhu, Jinge [1 ]
DeLuca, Hector F. [1 ]
机构
[1] Univ Wisconsin, Dept Biochem, Madison, WI 53706 USA
[2] Shaanxi Univ Technol, Vitamin Res Inst D, Xian, Shaanxi Provinc, Peoples R China
来源
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM | 2015年 / 308卷 / 03期
关键词
1,25-dihydroxyvitamin D; proximal renal tubule; vitamin D receptor; 24-hydroxylase; 1; alpha-hydroxylase; calcium; PARATHYROID-HORMONE; BIOLOGICAL-ACTIVITY; STIMULATION; 25-HYDROXYVITAMIN-D3; METABOLISM;
D O I
10.1152/ajpendo.00422.2014
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
It is well established that the mitochondria of proximal convoluted tubule cells of the kidney are the site of production of circulating 1 alpha,25-dihydroxyvitamin D-3 [1,25(OH)(2)D-3]. The production of 1,25(OH)(2)D-3 at this site is tightly regulated. Parathyroid hormone markedly stimulates 1,25(OH)(2)D-3 production, whereas 1,25(OH)(2)D-3 itself suppresses production. The mechanism of suppression by 1,25(OH)(2)D-3 has not yet been elucidated. We have now found that in the absence of vitamin D (vitamin D deficiency), the vitamin D receptor (VDR) is found in the interior of the apical brush border of the proximal tubule cells. This is unique for the proximal tubule cells, since this has not been observed in the distal tubule cells or in other epithelial cells, such as intestinal mucosa. Administration of 1,25(OH)(2)D-3 to vitamin D-deficient rats results in the movement of VDR from the brush border to the cytoplasm and nucleus presumably bound to reabsorbed 1,25(OH)(2)D-3. The VDR bound to 1,25(OH)(2)D-3 suppresses expression of 25-hydroxyvitamin D-3 1 alpha-hydroxylase and stimulates the 25-hydroxyvitamin D-3 24-hydroxylase. Thus, VDR in the apical brush border of the proximal convoluted tubule cells serves to "sense" the level of circulating 1,25(OH)(2)D-3 and modulates the activity of the 1 alpha-hydroxylase and the 24-hydroxylase accordingly.
引用
收藏
页码:E201 / E205
页数:5
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