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The local production of 1,25(OH)2D3 promotes osteoblast and osteocyte maturation
被引:39
|作者:
Turner, Andrew G.
[1
]
Hanrath, Maarten A.
[2
]
Morris, Howard A.
[1
]
Atkins, Gerald J.
[3
]
Anderson, Paul H.
[1
]
机构:
[1] Univ S Australia, Ctr Musculoskeletal Hlth Res, Sch Pharm & Med Sci, Adelaide, SA 5000, Australia
[2] Univ Utrecht, Sch Pharm, NL-3508 TC Utrecht, Netherlands
[3] Univ Adelaide, Ctr Orthopaed & Trauma Res, Adelaide, SA 5005, Australia
关键词:
Cyp27b1;
Vitamin D;
Osteocytes;
MLO-A5;
MLO-Y4;
VITAMIN-D;
GENE-EXPRESSION;
CELLS;
BONE;
MICE;
DIFFERENTIATION;
ESTABLISHMENT;
METABOLISM;
FRACTURE;
MLO-Y4;
D O I:
10.1016/j.jsbmb.2013.10.003
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Maintenance of an adequate vitamin D status, as indicated by the level of circulating 25-hydroxyvitamin D (25(OH)D), is associated with higher bone mass and decreased risk of fracture. However, the molecular actions of vitamin D hormone (1,25(OH)(2)D-3) in bone are complex, and include stimulation of osteoclastogenesis via RANK-ligand up-regulation, as well as the inhibition of mineralisation. We hypothesise that these divergent data may be reconciled by autocrine actions of 1,25(OH)(2)D-3 which effect skeletal maintenance, as opposed to endocrine 1,25(OH)(2)D-3 which acts to maintain serum calcium homeostasis. We have previously described local metabolism of 1,25(OH)(2)D-3 within osteoblasts, with effects on gene expression and cell function. The aim of the current study was to investigate potential autocrine actions of 1,25(OH)(2)D-3 within cells that exhibit osteocyte-like properties. Late osteoblastic MLO-A5 cells were cultured in the presence of 25(OH)D for 9 days with gene expression analysed pre- and post-mineralisation. Gene expression analysis revealed maturation within this time frame to an osteocyte-like stage, evidenced by increased Dmp1 and Phex mRNA expression. Expression of Cyp27b1 in 25(OH)D treated MLO-A5 cells was associated with elevated media levels of 1,25(OH)(2)D-3 (p < 0.05), induction of Cyp24a1 (p < 0.001) and elevated ratios of Opg:Rankl mRNA (p < 0.01). Chronic 25(OH)D exposure also increased osteocalcin mRNA in MLO-A5 cells, which contrasted with the dose-dependent inhibition of osteocalcin mRNA observed with acute treatment in MLO-Y4 cells (p < 0.01). Treatment of MLO-Y4 cells with 25(OH)D also inhibited Phex mRNA expression (p < 0.05), whilst Enpp1 gene expression was induced (p < 0.01). Overall, the current study demonstrates that osteocyte-like cells convert physiological levels of 25(OH)D to 1,25(OH)(2)D-3, with changes in gene expression that are consistent with increased osteocyte maturation. Although the physiological role of local metabolism of 1,25(OH)(2)D-3 within osteocytes requires further investigation, the abundance and diverse functions of this cell type within bone underscore its potential importance. This article is part of a Special Issue entitled '16th Vitamin D Workshop'. (C) 2013 Elsevier Ltd. All rights reserved.
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页码:114 / 118
页数:5
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