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釉基质衍生物在体外促进人牙周膜细胞分化及骨保护素生成。

Enamel matrix derivative promotes human periodontal ligament cell differentiation and osteoprotegerin production in vitro.

作者信息

Lossdörfer S, Sun M, Götz W, Dard M, Jäger A

机构信息

Department of Orthodontics, Dental Clinic, University of Bonn, Welschnonnenstr. 17, 53111 Bonn, Germany.

出版信息

J Dent Res. 2007 Oct;86(10):980-5. doi: 10.1177/154405910708601012.

Abstract

Enamel matrix derivative (EMD) has been used successfully to aid periodontal repair. We sought to elucidate the mechanism of action of EMD and hypothesized that combined exposure to EMD and parathyroid hormone (PTH), which acts anabolicly when administered intermittently, would enhance periodontal ligament cell proliferation, differentiation, and local factor production. Confluent human periodontal ligament cells were exposed to EMD continuously or to PTH(1-34) intermittently, or a combination of both. Cell number, alkaline phosphatase activity, osteocalcin, and osteoprotegerin production were determined. Continuous challenge with EMD resulted in an increase of the differentiation parameters and osteoprotegerin production, while simultaneously inhibiting proliferation. Intermittent PTH(1-34) administration exerted opposite effects. Combined administration of EMD and PTH(1-34) weakened or even nullified the effects seen for the agents alone. These results suggest that EMD promotes periodontal ligament cell differentiation and osteoprotegerin production, potentially resulting in a microenvironment supporting periodontal repair, whereas combining EMD and PTH(1-34) failed to prove beneficial in this respect.

摘要

釉基质衍生物(EMD)已成功用于辅助牙周修复。我们试图阐明EMD的作用机制,并假设联合使用EMD和甲状旁腺激素(PTH)(间歇性给药时具有合成代谢作用)会增强牙周膜细胞的增殖、分化和局部因子的产生。将汇合的人牙周膜细胞连续暴露于EMD或间歇性暴露于PTH(1-34),或两者联合使用。测定细胞数量、碱性磷酸酶活性、骨钙素和骨保护素的产生。连续用EMD刺激导致分化参数和骨保护素产生增加,同时抑制增殖。间歇性给予PTH(1-34)则产生相反的效果。联合给予EMD和PTH(1-34)会削弱甚至消除单独使用这些药物时所观察到的效果。这些结果表明,EMD促进牙周膜细胞分化和骨保护素产生,可能形成支持牙周修复的微环境,而在这方面联合使用EMD和PTH(1-34)并未显示出益处。

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