Kawashima H, Torikai S, Kurokawa K
Proc Natl Acad Sci U S A. 1981 Feb;78(2):1199-203. doi: 10.1073/pnas.78.2.1199.
Defined nephron segments were microdissected from the kidney of vitamin D-deficient rats, normal rats, and normal rats treated with 1 alpha, 25-dihydroxyvitamin D3 [1 alpha, 25-(OH)2D3]. Tubule segments were incubated with 3H]labeled 25-hydroxyvitamin D3 and the rates of production of 3H]labeled 1 alpha, 25-(OH)2D3 and 24,25-dihydroxyvitamin D3 [24,25-(OH)2D3] were determined. Nephron segments tested include the glomerulus, proximal convoluted tubules (PCT), proximal straight tubules (PST), medullary and cortical thick ascending limbs of Henle's loop, distal tubules, and collecting tubules. Production of 1 alpha, 25-(OH)2D3 was detected only in PCT of vitamin D-deficient rats (mean +/- SEM, 0.70 +/- 0.05 fmol/mm per hr); the value decreased to 0.11 +/- 0.05 after parathyroidectomy. By contrast, significant 24,25-(OH)2D3 production occurred in PCT of normal rats (0.23 +/- 0.05 fmol/mm per hr). After administration of 1 alpha, 25-(OH)2D3 to normal rats, the rate of production of 24,25-(OH)2D3 in PCT increased to 0.64 +/- 0.06 fmol/mm per hr and also became apparent in PST (1.07 +/- 0.21). The rates of production of 1 alpha, 25-(OH)2D3 and 24,25-(OH)2D3 in these nephron segments were linear with tubule length over a wide range of lengths per incubation and with the incubation time. The results define the localization of 25-hydroxyvitamin D3 1 alpha-hydroxylase and 24-hydroxylase along the rat nephron: PCT is capable of producing both 1 alpha, 25-(OH)2D3 and 24,25-(OH)2D3 and PST can produce 24,25-(OH)2D3. the use of defined nephron segments may be useful for study of the distribution and regulation of 25-hydroxyvitamin D3 hydroxylases in the kidney.
从维生素D缺乏的大鼠、正常大鼠以及用1α,25 - 二羟基维生素D3 [1α,25-(OH)2D3]处理的正常大鼠的肾脏中显微解剖出特定的肾单位节段。将肾小管节段与[3H]标记的25 - 羟基维生素D3一起孵育,并测定[3H]标记的1α,25-(OH)2D3和24,25 - 二羟基维生素D3 [24,25-(OH)2D3]的生成速率。所测试的肾单位节段包括肾小球、近端曲管(PCT)、近端直管(PST)、髓袢和皮质的亨氏袢厚升支、远端小管以及集合小管。仅在维生素D缺乏的大鼠的PCT中检测到1α,25-(OH)2D3的生成(平均值±标准误,0.70±0.05 fmol/mm每小时);甲状旁腺切除术后该值降至0.11±0.05。相比之下,正常大鼠的PCT中发生显著的24,25-(OH)2D3生成(0.23±0.05 fmol/mm每小时)。给正常大鼠施用1α,25-(OH)2D3后,PCT中24,25-(OH)2D3的生成速率增加至0.64±0.06 fmol/mm每小时,并且在PST中也变得明显(1.07±0.21)。在这些肾单位节段中,1α,25-(OH)2D3和24,25-(OH)2D3的生成速率在每次孵育的广泛长度范围内以及与孵育时间呈线性关系。这些结果确定了25 - 羟基维生素D3 1α - 羟化酶和24 - 羟化酶在大鼠肾单位中的定位:PCT能够生成1α,25-(OH)2D3和24,25-(OH)2D3,而PST能够生成24,25-(OH)2D3。使用特定的肾单位节段可能有助于研究肾脏中25 - 羟基维生素D3羟化酶的分布和调节。