Department of Oral Pathology, Osaka Dental University, Osaka, Japan.
J Periodontol. 2013 Oct;84(10):1476-83. doi: 10.1902/jop.2012.120469. Epub 2012 Nov 23.
In a previous study, the authors obtained a synthetic peptide (SP) for useful periodontal tissue regeneration. Periodontal ligament stem cells (PDLSCs) have multiple potentiality to contribute to tissue regeneration. The aim of this experiment is to investigate the effect of SP on human PDLSCs.
Periodontal ligament cells were obtained from healthy adult human third molars and used to isolate single PDLSC-derived colonies. The mesenchymal stem cell nature of the PDLSCs was confirmed by immunohistochemical evaluation of STRO-1 expression. Proliferation and osteoblastic differentiation were investigated by culturing PDLSCs in normal or osteogenic medium with and without SP (100 ng/mL). Osteoblast differentiation was assessed by measuring alkaline phosphatase (ALP) activity, osteocalcin production, mRNA expression of osteonectin, mineralization, and calcium deposition.
Isolated PDLSCs were immunohistochemically positive for vimentin and STRO-1 and negative for cytokeratin. A greater number of calcified nodules were observed in osteogenic medium culture with SP than without. In the early and later stages of PDLSC culture with SP, osteonectin production and osteocalcin production were increased. SP in culture with osteogenic medium significantly enhanced proliferation of PDLSCs, as well as ALP activity, expression of osteonectin, osteocalcin production, formation of calcified nodules, and mineralization.
SP enhances the formation of calcified nodules and osteocalcin production in the culture of PDLSCs into osteoblast-like cells and is a useful material for periodontal tissue regeneration.
在之前的一项研究中,作者获得了一种用于促进牙周组织再生的合成肽(SP)。牙周韧带干细胞(PDLSCs)具有多种组织再生的潜能。本实验旨在研究 SP 对人牙周韧带干细胞的影响。
从健康成人第三磨牙中获取牙周韧带细胞,用于分离单个牙周韧带干细胞衍生的克隆。通过 STRO-1 表达的免疫组织化学评估来确认 PDLSCs 的间充质干细胞特性。通过在含有或不含有 SP(100ng/ml)的正常或成骨培养基中培养 PDLSCs 来研究细胞增殖和成骨分化。通过测量碱性磷酸酶(ALP)活性、骨钙素产生、骨桥蛋白 mRNA 表达、矿化和钙沉积来评估成骨分化。
分离的 PDLSCs 免疫组织化学染色呈波形蛋白和 STRO-1 阳性,细胞角蛋白阴性。在含有 SP 的成骨培养基中培养的 PDLSCs 中观察到更多的钙化结节。在 PDLSC 培养过程中,早期和晚期添加 SP 均可增加骨桥蛋白和骨钙素的产生。SP 可显著增强成骨培养基中 PDLSCs 的增殖、ALP 活性、骨桥蛋白表达、骨钙素产生、钙化结节形成和矿化。
SP 可增强 PDLSCs 向成骨样细胞培养过程中钙化结节和骨钙素的形成,是牙周组织再生的有用材料。