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钙离子促进人牙髓细胞的成骨分化和矿化:对盖髓材料的启示。

Calcium ions promote osteogenic differentiation and mineralization of human dental pulp cells: implications for pulp capping materials.

机构信息

Department of Operative Dentistry and Endodontics, Guanghua School of Stomatology, Sun Yat-sen University, Guangzhou, People's Republic of China.

出版信息

J Mater Sci Mater Med. 2012 Mar;23(3):789-95. doi: 10.1007/s10856-011-4531-0. Epub 2011 Dec 22.

Abstract

Calcium (Ca) is the main element of most pulp capping materials and plays an essential role in mineralization. Different pulp capping materials can release various concentrations of Ca ions leading to different clinical outcomes. The purpose of this study was to investigate the effects of various concentrations of Ca ions on the growth and osteogenic differentiation of human dental pulp cells (hDPCs). Different concentrations of Ca ions were added to growth culture medium and osteogenic inductive culture medium. A Cell Counting Kit-8 was used to determine the proliferation of hDPCs in growth culture medium. Osteogenic differentiation and mineralization were measured by alkaline phosphatase (ALP) assay, Alizarin red S/von kossa staining, Ca content quantitative assay. The selected osteogenic differentiation markers were investigated by quantitative real-time polymerase chain reaction (qRT-PCR). Within the range of 1.8-16.2 mM, increased concentrations of Ca ions had no effect on cell proliferation, but led to changes in osteogenic differentiation. It was noted that enhanced mineralized matrix nodule formation was found in higher Ca ions concentrations; however, ALP activity and gene expression were reduced. qRT-PCR results showed a trend towards down-regulated mRNA expression of type I collagen and Runx2 at elevated concentrations of Ca ions, whereas osteopontin and osteocalcin mRNA expression were significantly up-regulated. Ca ions content in the culture media can significantly influence the osteogenic properties of hDPCs, indicating the importance of optimizing Ca ions release from dental pulp capping materials in order to achieve desirable clinical outcomes.

摘要

钙(Ca)是大多数牙髓盖髓材料的主要元素,在矿化过程中起着重要作用。不同的牙髓盖髓材料可释放不同浓度的 Ca 离子,从而导致不同的临床结果。本研究旨在探讨不同浓度的 Ca 离子对人牙髓细胞(hDPC)生长和成骨分化的影响。在生长培养基和成骨诱导培养基中分别添加不同浓度的 Ca 离子。使用细胞计数试剂盒-8 测定生长培养基中 hDPC 的增殖情况。通过碱性磷酸酶(ALP)测定、茜素红 S/von kossa 染色、钙含量定量测定来测量成骨分化和矿化。通过定量实时聚合酶链反应(qRT-PCR)检测选定的成骨分化标志物。在 1.8-16.2mM 范围内,增加 Ca 离子浓度对细胞增殖没有影响,但导致成骨分化发生变化。值得注意的是,在较高的 Ca 离子浓度下,增强的矿化基质结节形成;然而,ALP 活性和基因表达降低。qRT-PCR 结果显示,随着 Ca 离子浓度的升高,I 型胶原和 Runx2 的 mRNA 表达呈下调趋势,而骨桥蛋白和骨钙素的 mRNA 表达显著上调。培养基中 Ca 离子含量可显著影响 hDPC 的成骨特性,这表明优化牙髓盖髓材料中 Ca 离子释放以达到理想的临床效果非常重要。

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