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生长分化因子 5 和骨形态发生蛋白 2 对人牙周膜来源细胞肌腱/韧带形成相关标志物表达的影响。

Effect of GDF-5 and BMP-2 on the expression of tendo/ligamentogenesis-related markers in human PDL-derived cells.

机构信息

Department of Oral and Maxillofacial Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.

出版信息

Oral Dis. 2012 Mar;18(2):206-12. doi: 10.1111/j.1601-0825.2011.01871.x. Epub 2011 Nov 18.

DOI:10.1111/j.1601-0825.2011.01871.x
PMID:22093095
Abstract

OBJECTIVES

The effect of growth differentiation factor 5 and bone morphogenetic protein 2 on human periodontal ligament-derived cells was investigated with special reference to tendo/ligamentogenesis-related markers.

MATERIALS AND METHODS

Effects of each factor were analyzed by quantitative PCR for scleraxis and tenomodulin and by western blotting for scleraxis. After exposure to those factors, STRO-1-positive and STRO-1-negative fractions of human periodontal ligament tissues were isolated with an immunomagnetic cell sorting system, and the expression of scleraxis in each fraction was analyzed by western blotting. Non-separated crude cells were used as a control.

RESULTS

Growth differentiation factor 5 and bone morphogenetic protein 2 did not increase alkaline phosphatase activity in crude periodontal ligament-derived cells. Growth differentiation factor 5, but not bone morphogenetic protein 2, increased the expression of scleraxis in crude, STRO-1-positive and STRO-1-negative periodontal ligament-derived cells. The expression of scleraxis in STRO-1-positive periodontal ligament-derived cells was significantly less compared to that in crude P2 and STRO-1-negative periodontal ligament-derived cells.

CONCLUSION

Growth differentiation factor 5 induced the expression of scleraxis and may enhance tendo/ligamentogenesis in human periodontal ligament-derived cells. The expression of scleraxis was higher in STRO-1-negative fraction, suggesting more differentiated state of the cells.

摘要

目的

研究生长分化因子 5 和骨形态发生蛋白 2 对人牙周膜源性细胞的影响,特别关注与腱/韧带发生相关的标记物。

材料与方法

通过定量 PCR 分析每个因子对硬骨形成蛋白和肌腱蛋白聚糖的影响,并通过 Western blot 分析硬骨形成蛋白。在暴露于这些因子后,使用免疫磁细胞分选系统分离人牙周膜组织中 STRO-1 阳性和 STRO-1 阴性细胞,并通过 Western blot 分析每个部分的硬骨形成蛋白表达。未分离的粗细胞作为对照。

结果

生长分化因子 5 和骨形态发生蛋白 2 不会增加粗牙周膜源性细胞中的碱性磷酸酶活性。生长分化因子 5 但不是骨形态发生蛋白 2 增加了粗、STRO-1 阳性和 STRO-1 阴性牙周膜源性细胞中硬骨形成蛋白的表达。与粗 P2 和 STRO-1 阴性牙周膜源性细胞相比,STRO-1 阳性牙周膜源性细胞中硬骨形成蛋白的表达明显减少。

结论

生长分化因子 5 诱导硬骨形成蛋白的表达,并可能增强人牙周膜源性细胞中的腱/韧带发生。STRO-1 阴性部分中硬骨形成蛋白的表达较高,表明细胞的分化状态更高。

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