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骨钙素信使核糖核酸在大鼠骨肉瘤细胞中受1,25 - 二羟维生素D3和3',5'-环磷酸腺苷调控。

Bone Gla protein messenger ribonucleic acid is regulated by both 1,25-dihydroxyvitamin D3 and 3',5'-cyclic adenosine monophosphate in rat osteosarcoma cells.

作者信息

Theofan G, Price P A

机构信息

Department of Biology, University of California, San Diego, La Jolla 92093.

出版信息

Mol Endocrinol. 1989 Jan;3(1):36-43. doi: 10.1210/mend-3-1-36.

DOI:10.1210/mend-3-1-36
PMID:2464756
Abstract

1,25-Dihydroxyvitamin D3 [1,25-(OH)2D3] regulates the synthesis of bone gamma-carboxyglutamic acid (Gla) protein (BGP) by osteoblastic cells. In this study we examined the effect of cAMP, alone and in combination with 1,25-(OH)2D3, on the regulation of BGP mRNA levels in ROS 17/2 rat osteosarcoma cells. Elevation of intracellular cAMP levels by cAMP analogs or by isobutylmethylxanthine (IBMX), forskolin, or PTH, resulted in increased BGP mRNA levels and BGP secretion after 1 day of treatment. The effects of these agents were additive with 1,25-(OH)2D3 in stimulating BGP gene expression. After 4 days of treatment, pertussis toxin (PT) and 1,25-(OH)2D3 were synergistic in stimulating BGP mRNA, and the effect of PT could be mimicked by (Bu)2cAMP, IBMX, forskolin, cholera toxin, and to a lesser extent by PTH. The effect of 1-day treatment with cAMP alone and the synergistic effect with 1,25-(OH)2D3 on the stimulation of BGP mRNA were dependent on cell density, while basal and 1,25-(OH)2D3-stimulated synthesis were not. Cyclic AMP inhibited ROS 17/2 cell growth after 1 day of treatment, an effect that was also dependent on initial cell density. After 4 days of treatment, 1,25-(OH)2D3, cAMP, and PT all demonstrated inhibition of cell growth. When cells were treated with actinomycin D, both 1,25-(OH)2D3 and cAMP stimulation of BGP mRNA were blocked. In addition, neither agent was effective in enhancing BGP mRNA stability when prestimulated cells were exposed to actinomycin D.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

1,25 - 二羟基维生素D3[1,25 - (OH)2D3]可调节成骨细胞合成骨γ - 羧基谷氨酸(Gla)蛋白(BGP)。在本研究中,我们检测了环磷酸腺苷(cAMP)单独及与1,25 - (OH)2D3联合使用时,对ROS 17/2大鼠骨肉瘤细胞中BGP mRNA水平调节的影响。用cAMP类似物、异丁基甲基黄嘌呤(IBMX)、福斯可林或甲状旁腺激素(PTH)提高细胞内cAMP水平,处理1天后可导致BGP mRNA水平升高及BGP分泌增加。这些试剂与1,25 - (OH)2D3在刺激BGP基因表达方面具有相加作用。处理4天后,百日咳毒素(PT)与1,25 - (OH)2D3在刺激BGP mRNA方面具有协同作用,且PT的作用可被双丁酰环磷腺苷((Bu)2cAMP)、IBMX、福斯可林、霍乱毒素模拟,甲状旁腺激素的模拟作用较弱。单独用cAMP处理1天对BGP mRNA的刺激作用以及与1,25 - (OH)2D3的协同作用取决于细胞密度,而基础合成及1,25 - (OH)2D3刺激的合成则不受其影响。处理1天后,环磷酸腺苷抑制ROS 17/2细胞生长,此作用也取决于初始细胞密度。处理4天后,1,25 - (OH)2D3、环磷酸腺苷和百日咳毒素均表现出对细胞生长的抑制作用。当用放线菌素D处理细胞时,1,25 - (OH)2D3和环磷酸腺苷对BGP mRNA的刺激作用均被阻断。此外,当预先刺激的细胞暴露于放线菌素D时,这两种试剂在增强BGP mRNA稳定性方面均无效。(摘要截短于250字)

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