Journal of Oral Science Research ›› 2017, Vol. 33 ›› Issue (12): 1246-1249.DOI: 10.13701/j.cnki.kqyxyj.2017.12.002

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Study on Anti-inflammatory Effects of PMX205 in Vitro

LI Ge-ge1, TANG Qiu-ling1, PAN Jia-hui1, WANG Liu-ran1, MENG Yang1, YUE Yi-yun1, DING Xiao-han1, LIU Dong-ning1, YU Wei-xian1,2,3*   

  1. 1. Department of Periodontics, School of Stomatology, Jilin University, Changchun 130021, China;
    2. Experimental Teaching Center, School of Stomatology, Jilin University, Changchun 130021, China;
    3. Jilin Provincial Key Laboratory of Tooth Development and Bone Remodeling, Changchun 130021, China.
  • Received:2017-06-08 Online:2017-12-20 Published:2018-01-03

Abstract: Objective: To explore the anti-inflammatory effects of C5aR antagonist PMX205. Methods: The toxicity of PMX205 for the mouse macrophage (RAW264.7) was tested with MTT assay. RAW264.7 cells were co-cultured with gingipains (G) to simulate the inflammatory environment in vitro and the anti-inflammatory effects of PMX205 was observed. The experiment was divided into six groups: negative control group, G group, and G + PMX205(0.1,1,5,10 mg/L)group. After cultured for 24 h, qRT-PCR and ELISA were used to detect IL-6, TNF-α, IL-10 and TGF-β1. Flow cytometry was used to detect the M1 marker molecule CD86 and M2 marker molecule CD206. Results: MTT results showed that PMX205 had little effect on the viability of RAW264.7. qRT-PCR and ELISA results showed that IL-6 and TNF-α expression levels of G group were higher than the negative control group. The expression of IL-6 and TNF-α were decreased in G + PMX205 group, and TGF-β1 and IL-10 were higher than those in G group. Flow cytometry showed that CD86 positive rate was increased and the CD206 positive rate was decreased in G group. In G+PMX205 group the CD86 was decreased, the CD206 was higher than those in G group. Conclusion: In vitro cell model experiments, PMX205 showed good anti-inflammatory effects

Key words: Periodontitis , Gingipain , PMX205, Macrophage , Polarization

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