Objective:To investigate the influence and mechanism of Porphyromonas gingivalis (P.g) lipopolysaccharide (LPS) on osteogenic differentiation of human periodontal ligament cells (HPDLCs). Methods:HPDLCs were obtained from the primary culture of the tissues,and cultured in alpha-MEM (group A) and osteogenic induced medium (group B), as well as osteogenic induced medium containing 1 μg/mL P.g LPS (group C). The proliferation ability of HPDLSCs was analyzed by MTT assay. Alkaline phosphatase (ALP) staining and Alizarin red staining were applied to detect the mineralization ability. The expression levels of osteogenic differentiation related-genes collagen I (COL1), alkaline phosphatase (ALP), runt-related transcription factor 2 (RUNX2) and osteocalcin (OCN) were detected by real-time PCR. Results:No obvious difference in cell proliferation was found between group B and group C (P>0.05). ALP staining and alizarin red staining in group B and group C were positive. Compared with group A, OD values in group B and group C were significantly increased (P<0.05), but the OD value in group C was lower than that in group B (P<0.05). Although the expression of osteogenic differentiation related-genes increased significantly in group B and group C, the levels of these genes were higher in group B than that in group C (P<0.05). Conclusion:P.g LPS has negative effect on osteogenic differentiation ability of HPDLCs through inhibiting the expressions of osteogenic differentiation related-genes, resulting in impaired self-repair of periodontal tissue.
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作者简介 薛栋(1987-),女,硕士在读,研究方向:牙周炎发病机制; 通信作者:蒋少云,E-mail:jiangshaoyun11@126.com。