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维生素 D(3)代谢物可诱导人牙髓和人齿槽突细胞的成骨分化。

Vitamin D(3) metabolites induce osteogenic differentiation in human dental pulp and human dental follicle cells.

机构信息

REGEA, Institute for Regenerative Medicine, University of Tampere and Tampere University Hospital, Biokatu-12, 33520 Tampere, Finland.

出版信息

J Steroid Biochem Mol Biol. 2010 Oct;122(4):133-41. doi: 10.1016/j.jsbmb.2010.08.001. Epub 2010 Aug 17.

Abstract

Vitamin D(3) metabolites regulate the bone metabolism and 1α,25-dihydroxyvitamin D(3) (1α,25(OH)(2)D(3)) is known to play an important role in teeth mineralization. However, little is known about the potential of vitamin D as an osteogenic inducer in human dental pulp (hDPCs) and dental follicle cells (hDFCs) in vitro. Therefore, we investigated the effects of vitamin D(3) metabolites 1α,25(OH)(2)D(3) and 25-hydroxyvitamin D(3) (25OHD(3)) on proliferation and osteogenic differentiation of hDPCs and hDFCs in vitro. We also examined whether vitamin D(3) metabolic enzymes were regulated in hDFCs and hDPCs. Cell proliferation was decreased by both metabolites in hDPCs and hDFCs. Vitamin D(3) metabolites increased ALP activity and induced mineralization when osteogenic supplements (OS; l-ascorbic acid-2-phosphate+β-glycerophosphate) were added, though the expression of osteocalcin (OC) and osteopontin (OPN) were regulated without the addition of OS. CYP24 and CYP27B1 expressions were upregulated by vitamin D(3) metabolites and 25OHD(3) was converted into 1α,25(OH)(2)D(3) in the culture medium. These results confirm that 1α,25(OH)(2)D(3) (10 and 100 nM) and 25OHD(3) (500 nM) can be used as osteogenic inducers synergistically with osteogenic supplements for differentiation of hDPCs and hDFCs. Furthermore, our findings strengthen our knowledge about the role of hDPCs and hDFCs as vitamin D(3) target cells.

摘要

维生素 D(3)代谢物调节骨代谢,1α,25-二羟维生素 D(3)(1α,25(OH)(2)D(3))被认为在牙齿矿化中发挥重要作用。然而,关于维生素 D 作为体外人牙髓细胞(hDPCs)和牙囊细胞(hDFCs)成骨诱导剂的潜力知之甚少。因此,我们研究了维生素 D(3)代谢物 1α,25(OH)(2)D(3)和 25-羟维生素 D(3)(25OHD(3))对 hDPCs 和 hDFCs 体外增殖和成骨分化的影响。我们还检查了维生素 D(3)代谢酶是否在 hDFCs 和 hDPCs 中受到调节。两种代谢物均降低了 hDPCs 和 hDFCs 的细胞增殖。当添加成骨补充剂(l-抗坏血酸-2-磷酸+β-甘油磷酸)时,维生素 D(3)代谢物增加了碱性磷酸酶(ALP)活性并诱导矿化,尽管在不添加 OS 的情况下调节了骨钙素(OC)和骨桥蛋白(OPN)的表达。CYP24 和 CYP27B1 的表达被维生素 D(3)代谢物上调,并且 25OHD(3)在培养基中转化为 1α,25(OH)(2)D(3)。这些结果证实 1α,25(OH)(2)D(3)(10 和 100 nM)和 25OHD(3)(500 nM)可与成骨补充剂协同用作 hDPCs 和 hDFCs 分化的成骨诱导剂。此外,我们的研究结果增强了我们对 hDPCs 和 hDFCs 作为维生素 D(3)靶细胞的作用的认识。

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