Walters M R, Ilenchuk T T, Claycomb W C
J Biol Chem. 1987 Feb 25;262(6):2536-41.
This study tested the hypothesis that 1,25-dihydroxyvitamin D3 (1,25-(OH)2D3) and its previously described cardiac receptors play roles in regulating intracellular calcium homeostasis in cardiac muscle cells. This question was addressed by assessing whether 1,25-(OH)2D3 influences 45Ca2+ uptake by homogeneous cultures of adult rat ventricular cardiac muscle cells. Twenty-four h prior to the measurement of 45Ca2+ uptake, the cells were transferred to serum-free medium ([Ca2+], 1.0 mM) containing 1.0 nM 1,25(OH)2D3 or vehicle. The cells were then incubated with 45Ca2+ for periods up to 60 min at room temperature, followed by removal of excess external 45Ca2+ by washing repeatedly with La3+. Pretreating the cells with 1,25-(OH)2D3 caused 3-fold stimulation (p less than 0.005) of 45Ca2+ uptake. Stimulation of 45Ca2+ uptake required a prolonged (8-12 h) exposure to 1,25-(OH)2D3, suggesting a receptor-mediated phenomenon. Concentrations of 0.01-10 nM 1,25-(OH)2D3 yielded a dose-response curve which peaked at 1.0 nM and decreased at higher concentrations. Steroid specificity was established by the failure of 1.0 nM levels of 25-hydroxyvitamin D3, estradiol-17 beta, and progesterone to change 45Ca2+ uptake. Sucrose gradient analysis confirmed the presence of a specific 3-4 S 3H-1,25-(OH)2D3 binding component both in freshly isolated and in cultured ventricular cardiac muscle cells. The stimulatory effect of 1,25-(OH)2D3 on 45Ca2+ uptake was abolished by the concomitant incubation of the cells with cycloheximide or actinomycin D, demonstrating a requirement for protein and nucleic acid synthesis. In conclusion, these data demonstrate that 1,25-(OH)2D3 stimulates 45Ca2+ uptake in adult ventricular cardiac muscle cells by a mechanism resembling a receptor-mediated phenomenon.
1,25 - 二羟基维生素D3(1,25-(OH)2D3)及其先前描述的心脏受体在调节心肌细胞内钙稳态中发挥作用。通过评估1,25-(OH)2D3是否影响成年大鼠心室心肌细胞均匀培养物对45Ca2+的摄取来解决这个问题。在测量45Ca2+摄取前24小时,将细胞转移至含有1.0 nM 1,25(OH)2D3或溶剂的无血清培养基([Ca2+],1.0 mM)中。然后将细胞与45Ca2+在室温下孵育长达60分钟,随后用La3+反复洗涤以去除过量的细胞外45Ca2+。用1,25-(OH)2D3预处理细胞导致45Ca2+摄取增加3倍(p小于0.005)。45Ca2+摄取的刺激需要长时间(8 - 12小时)暴露于1,25-(OH)2D3,提示这是一种受体介导的现象。0.01 - 10 nM的1,25-(OH)2D3浓度产生了一条剂量 - 反应曲线,该曲线在1.0 nM时达到峰值,在更高浓度时下降。1.0 nM水平的25 - 羟基维生素D3、雌二醇 - 17β和孕酮未能改变45Ca2+摄取,从而确立了类固醇特异性。蔗糖梯度分析证实,在新鲜分离的和培养的心室心肌细胞中均存在一种特异性的3 - 4 S 3H - 1,25-(OH)2D3结合成分。细胞与放线菌酮或放线菌素D共同孵育可消除1,25-(OH)2D3对45Ca2+摄取的刺激作用,表明蛋白质和核酸合成是必需的。总之,这些数据表明1,25-(OH)2D3通过一种类似于受体介导的现象的机制刺激成年心室心肌细胞对45Ca2+的摄取。