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作 者:姚丽艳[1] 黄美香[1] 钟泉[1] 郑瑜谦[1] 李大兰[1] 骆凯[1] 闫福华[1]
机构地区:[1]福建医科大学口腔医学院,福建省高校口腔医学重点实验室,福州350002
出 处:《中国医科大学学报》2012年第8期719-722,共4页Journal of China Medical University
基 金:福建省科技重点项目(2009Y0019);福建医科大学临床医学重点学科建设项目(XK201111)
摘 要:目的探讨环孢素A(CsA)联合牙龈卟啉单胞菌脂多糖(Pg-LPS)对人牙周膜成纤维细胞(PDLFs)生物学活性的影响。方法将CsA(100 ng/mL)、LPS(100 ng/mL)分别单独及联合作用于人PDLFs,采用考马斯亮蓝染色、ELISA、Von kossa染色等方法检测其对PDLFs总蛋白量、碱性磷酸酶(ALP)、骨形成蛋白2(BMP-2)及矿化结节形成的影响。结果 CsA单独及与LPS联合应用可促进细胞总蛋白的合成,增加细胞ALP活性及BMP-2的表达,并促进细胞矿化结节的早期形成;LPS单独应用可增加细胞的ALP活性,但对细胞的总蛋白合成、BMP-2的表达及矿化结节的早期形成无明显影响。结论一定浓度的CsA促PDLFs合成、分化作用明显,CsA联合LPS在促进细胞分化方面具有一定的协同作用。Objective To evaluate the in vitro effects of cyclosporine A (CsA) and Porphyromonas gingivalis-lipopolysaccharide(Pg-LPS) on the biological activity of human periodontal ligament fibroblasts (hPDLFs). Methods hPDLFs were incubated with CsA 100 ng/mL, Pg- LPS 100 ng/mL,CsA 100 ng/mL+Pg-LPS 100 ng/mL. Then the total protein was extracted and the concentration was assessed with Coomassie brilliant blue. Several features such as expression of bone morphogenetic protein-2(BMP-2) and alkaline phosphatase(ALP) were detected by enzyme-linked immunosorbent assay (ELISA). The formation of mineralized islets was assessed by Von kossa staining. Results CsA alone or plus LPS could significantly enhanced the total protein concentration, ALP, BMP-2 and mineralized islets of hPDLFs; LPS alone could significantly promote cells ALP expression,whereas has no significant effect on protein concentration, BMP-2 and mineralized islets of hPDLFs. Conclusion At certain concentrations, CsA could significantly enhance hPDLFs biological activity, synergistic effect was observed on enhancing cell differentiation when combined with LPS.
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