Journal of Oral Science Research ›› 2016, Vol. 32 ›› Issue (6): 580-583.DOI: 10.13701/j.cnki.kqyxyj.2016.06.007

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Effects of MT01 on the ALP Activity and mRNA Expression of MG63 Infected by Porphyromonas Gingivalis.

GAO Han1,2, SHEN Yu-qin1, LIU Yin1,2, HU Tian-qi1,2, FEI Hong-bo1,2, GU Zhong-yi1,2, LI Yang-yang1,2, LIN Chong-tao1*.   

  1. 1. Dept. of Periodontology, School and Hospital of Stomatology, Jilin University, Changchun 130021, China;
    2. Jilin Provincial Key Laboratory of Tooth Development and Bone Remodeling, Changchun 130021, China
  • Received:2015-12-28 Online:2016-06-26 Published:2016-06-22

Abstract: Objective: To study the effect of MT01 on the differentiation of osteoblasts infected by porphyromonas gingivalis (Pg). Methods: The MG63 cells were seeded into 6- well cell culture plates. MT01 at a final concentration of 1 μg·mL-1 was added and incubated for 3 hours. Then the cells were challenged by Pg (MOI=100∶1). There were four experimental groups: blank group, MT01, Pg and MT01+Pg. ALP activities in the supernatant fluid and the cell lysate after 24 hours were detected by ALP kit. Real-time PCR was used to detect the mRNA expression of ALP after 2, 4, 6, 8, 12, and 24 hours. Results: MT01 enhanced the ALP activity in infected or uninfected conditions. The mRNA expression of ALP in MG63 was upregulated by MT01 post-infected by Pg or not in a time-dependent manner. Conclusion: MT01 can upregulate the mRNA expression of ALP in Pg infected or uninfected MG63 and improve the ALP activity.

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