Condamine L, Menaa C, Vrtovsnik F, Friedlander G, Garabédian M
CNRS URA 583, Hôpital Saint Vincent de Paul, Paris, France.
J Clin Invest. 1994 Oct;94(4):1673-9. doi: 10.1172/JCI117512.
The hormonal form of vitamin D, 1,25(OH)2D, is synthesized mostly in proximal renal tubular cells. Experimental and clinical studies suggest that the growth hormone may be involved in growth-related fluctuations of plasma 1,25(OH)2D and in the increase of 1,25(OH)2D induced by in vivo phosphate deprivation, an action possibly mediated by insulin-like growth factor 1 (IGF 1). We tested the effects of phosphate depletion and IGF 1 addition on 1,25(OH)2D3 production in cultured kidney cells: opossum kidney (OK) cells, LLC-PK 1, and rabbit's proximal tubular cells. Confluent cell monolayers were preincubated in various phosphate concentrations, in the presence and absence of IGF 1. Then, 5 nM of [3H]25 (OH)D3 or 2 microM of 25 (OH)D3 were added to the medium and the cells were incubated for a further 120 min. The amount of biosynthesized 1,25(OH)2D3 in lipid extracts was determined after two different straight phase high performance liquid chromatographies. The experiment showed the following: (a) LLC-PK 1 and rabbit's cells expressed a detectable ability to synthesize 1,25(OH)2D3, while OK cells did not. (b) Partial or total phosphate deprivation increased the amount of 1,25(OH)2D3 produced, respectively in LLC-PK 1 and in rabbit's cells. (c) IGF 1 (25 ng/ml) increased 1,25(OH)2D3 production in rabbit's cells, particularly in phosphate-free medium (1.6-fold), and in LLC-PK 1 cells, in partial phosphate depletion (2.75-fold in 1 mM phosphate, P = 0.015, n = 5, and 3.2-fold in 0.5 mM phosphate, P = 0.043, n = 4). Our findings demonstrate a local action of phosphate depletion and of IGF 1 on 1,25-dihydroxyvitamin D3 production.
维生素D的激素形式,即1,25(OH)2D,主要在近端肾小管细胞中合成。实验和临床研究表明,生长激素可能参与血浆1,25(OH)2D与生长相关的波动,以及体内磷酸盐缺乏诱导的1,25(OH)2D增加,这一作用可能由胰岛素样生长因子1(IGF 1)介导。我们测试了磷酸盐缺乏和添加IGF 1对培养的肾细胞(负鼠肾(OK)细胞、LLC-PK 1细胞和兔近端肾小管细胞)中1,25(OH)2D3产生的影响。将汇合的细胞单层在存在和不存在IGF 1的情况下,于不同磷酸盐浓度中预孵育。然后,向培养基中加入5 nM的[3H]25(OH)D3或2 μM的25(OH)D3,细胞再孵育120分钟。经过两次不同的正相高效液相色谱法后,测定脂质提取物中生物合成的1,25(OH)2D3的量。实验结果如下:(a)LLC-PK 1细胞和兔细胞表现出可检测到的合成1,25(OH)2D3的能力,而OK细胞则没有。(b)部分或完全磷酸盐缺乏分别增加了LLC-PK 1细胞和兔细胞中1,25(OH)2D3的产生量。(c)IGF 1(25 ng/ml)增加了兔细胞中1,25(OH)2D3的产生,特别是在无磷酸盐培养基中(增加1.6倍),以及在部分磷酸盐缺乏的LLC-PK 1细胞中(在1 mM磷酸盐中增加2.75倍,P = 0.015,n = 5;在0.5 mM磷酸盐中增加3.2倍,P = 0.043,n = 4)。我们的研究结果证明了磷酸盐缺乏和IGF 1对1,25-二羟基维生素D3产生的局部作用。