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机械负荷与原代人成骨细胞中1,25(OH)₂D的合成

Mechanical loading and the synthesis of 1,25(OH)2D in primary human osteoblasts.

作者信息

van der Meijden K, Bakker A D, van Essen H W, Heijboer A C, Schulten E A J M, Lips P, Bravenboer N

机构信息

Department of Internal Medicine/Endocrinology, VU University Medical Center, Research Institute MOVE, Amsterdam, The Netherlands.

Department of Oral Cell Biology, Academic Centre for Dentistry Amsterdam (ACTA) and VU University Amsterdam, Research Institute MOVE, Amsterdam, The Netherlands.

出版信息

J Steroid Biochem Mol Biol. 2016 Feb;156:32-9. doi: 10.1016/j.jsbmb.2015.11.014. Epub 2015 Nov 25.

Abstract

The metabolite 1,25-dihydroxyvitamin D (1,25(OH)2D) is synthesized from its precursor 25-hydroxyvitamin D (25(OH)D) by human osteoblasts leading to stimulation of osteoblast differentiation in an autocrine or paracrine way. Osteoblast differentiation is also stimulated by mechanical loading through activation of various responses in bone cells such as nitric oxide signaling. Whether mechanical loading affects osteoblast differentiation through an enhanced synthesis of 1,25(OH)2D by human osteoblasts is still unknown. We hypothesized that mechanical loading stimulates the synthesis of 1,25(OH)2D from 25(OH)D in primary human osteoblasts. Since the responsiveness of bone to mechanical stimuli can be altered by various endocrine factors, we also investigated whether 1,25(OH)2D or 25(OH)D affect the response of primary human osteoblasts to mechanical loading. Primary human osteoblasts were pre-incubated in medium with/without 25(OH)D3 (400 nM) or 1,25(OH)2D3 (100 nM) for 24h and subjected to mechanical loading by pulsatile fluid flow (PFF). The response of osteoblasts to PFF was quantified by measuring nitric oxide, and by PCR analysis. The effect of PFF on the synthesis of 1,25(OH)2D3 was determined by subjecting osteoblasts to PFF followed by 24h post-incubation in medium with/without 25(OH)D3 (400 nM). We showed that 1,25(OH)2D3 reduced the PFF-induced NO response in primary human osteoblasts. 25(OH)D3 did not significantly alter the NO response of primary human osteoblasts to PFF, but 25(OH)D3 increased osteocalcin and RANKL mRNA levels, similar to 1,25(OH)2D3. PFF did not increase 1,25(OH)2D3 amounts in our model, even though PFF did increase CYP27B1 mRNA levels and reduced VDR mRNA levels. CYP24 mRNA levels were not affected by PFF, but were strongly increased by both 25(OH)D3 and 1,25(OH)2D3. In conclusion, 1,25(OH)2D3 may affect the response of primary human osteoblasts to mechanical stimuli, at least with respect to NO production. Mechanical stimuli may affect local vitamin D metabolism in primary human osteoblasts. Our results suggest that 1,25(OH)2D3 and mechanical loading, both stimuli of the differentiation of osteoblasts, interact at the cellular level.

摘要

代谢物1,25 - 二羟基维生素D(1,25(OH)2D)由其前体25 - 羟基维生素D(25(OH)D)经人成骨细胞合成,以自分泌或旁分泌方式刺激成骨细胞分化。机械负荷通过激活骨细胞中的各种反应(如一氧化氮信号传导)也能刺激成骨细胞分化。机械负荷是否通过增强人成骨细胞对1,25(OH)2D的合成来影响成骨细胞分化尚不清楚。我们推测机械负荷刺激原代人成骨细胞从25(OH)D合成1,25(OH)2D。由于骨对机械刺激的反应性可被多种内分泌因子改变,我们还研究了1,25(OH)2D或25(OH)D是否影响原代人成骨细胞对机械负荷的反应。原代人成骨细胞在含有/不含25(OH)D3(400 nM)或1,25(OH)2D3(100 nM)的培养基中预孵育24小时,然后通过脉动流体流(PFF)施加机械负荷。通过测量一氧化氮和PCR分析来量化成骨细胞对PFF的反应。通过使成骨细胞接受PFF,然后在含有/不含25(OH)D3(400 nM)的培养基中孵育24小时后,测定PFF对1,25(OH)2D3合成的影响。我们发现1,25(OH)2D3降低了原代人成骨细胞中PFF诱导的一氧化氮反应。25(OH)D3并未显著改变原代人成骨细胞对PFF的一氧化氮反应,但25(OH)D3增加了骨钙素和RANKL mRNA水平,与1,25(OH)2D3相似。在我们的模型中,PFF并未增加1,25(OH)2D3的量,尽管PFF确实增加了CYP27B1 mRNA水平并降低了VDR mRNA水平。CYP24 mRNA水平不受PFF影响,但25(OH)D3和1,25(OH)2D3均使其显著增加。总之,1,25(OH)2D3可能影响原代人成骨细胞对机械刺激的反应,至少在一氧化氮产生方面。机械刺激可能影响原代人成骨细胞中的局部维生素D代谢。我们的结果表明,1,25(OH)2D3和机械负荷这两种成骨细胞分化的刺激因素在细胞水平上相互作用。

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