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Updated: Mar 11, 2026

Inducing Apical Periodontitis in Mice
Published on: August 6, 2019
[Mechanism of TNF-α in bone defect of chronic apical periodontitis]
Ya-Qiong Yu1, Liu Qu, Li-Hong Qiu
1Department of Endodontics,School of Stomatology,China Medical University; Lab of Endodontic,Liaoning Institute of Dental Research;Liaoning Provincial Research Center of Translational Oral Medicine. Shenyang 110002, China.
Purpose:
To investigate the effect of lipopolysaccharides(LPS) extracted from Porphyromonas endodontalis(P.e) on the expression of tumor necrosis factor-α(TNF-α) mRNA in MC3T3-E1 cells and the role of NF-κB signaling on the expression of macrophage colony stimulating factor (M-CSF) induced by TNF-α in MC3T3-El cells. METHODS: MC3T3-E1 cells were treated with different concentrations of P.e-LPS(0-50 mg/L) and 10 mg/L P.e-LPS for different time (0-24 h). The expression of TNF-α mRNA was detected by reverse transcription polymerase chain reaction(RT-PCR). MC3T3-E1 cells were treated with different concentrations of TNF-α(0-10 ng/L) for 6 h. The expression of M-CSF mRNA and protein was detected by RT-PCR and enzyme-linked immunoadsordent assay(ELISA).The expression of M-CSF protein was also detected in 10 ng/L TNF-α treated MC3T3-E1 cells after pretreated with BAY 11-7082 for 1 h, a special NF-κB inhibitor . Statistical analysis was performed using Multi-way ANOVA and Dunnett t test with SPSS 13.0 software package.
Results:
The level of TNF-α mRNA increased significantly after treatment with different concentrations of P.e-LPS(0-50 mg/L),which indicated that P.e-LPS induced osteoblasts to express TNF-α mRNA in dose dependent manners. Maximal induction of TNF-α mRNA expression was seen in the MC3T3-E1 cells treated with 10 mg/L P.e-LPS for 6 h. After 6 h, the expression of TNF-α mRNA decreased gradually .The expression of M-CSF mRNA and protein was increased in a does- dependent manner by different concentrations of TNF-α treatment(0-10 ng/L). The expression of M-CSF protein increased from (37±2) ng/L(control group) to (301±8) ng/L(10 ng/L group).The protein of M-CSF decreased significantly after pretreatment with 10 μmol/L BAY 11-7082 for 1 h, and the expression of M-CSF proteins was reduced from (253±14) ng/L to (154±2) ng/L .BAY group had no significant difference from the control group.
Conclusions:
The expression of TNF-α mRNA was increased by P. endodontalis LPS treatment in osteoblast. TNF-α may induce the expression of M-CSF in MC3T3-E1 cells through the signaling of NF-κB. It suggests that TNF-α affect osteoblasts through autocrine way for bone destruction in chronic apical periodontitis induced by P.e-LPS.
Insights
Porphyromonas endodontalis lipopolysaccharides (P.e-LPS) increase tumor necrosis factor-alpha (TNF-α) mRNA in osteoblasts. TNF-α then induces macrophage colony-stimulating factor (M-CSF) via NF-κB signaling, suggesting autocrine bone destruction in periodontitis.
Area of Science:
- Cell Biology
- Immunology
- Oral Biology
Background:
- Chronic apical periodontitis involves bone destruction.
- Porphyromonas endodontalis lipopolysaccharides (P.e-LPS) are implicated in periodontitis.
- Osteoblasts play a role in bone remodeling and immune responses.
Purpose of the Study:
- To investigate the effect of P.e-LPS on TNF-α mRNA expression in MC3T3-E1 osteoblasts.
- To determine the role of NF-κB signaling in TNF-α-induced M-CSF expression in MC3T3-E1 cells.
Main Methods:
- MC3T3-E1 cells were treated with varying concentrations and durations of P.e-LPS.
- TNF-α mRNA expression was quantified using RT-PCR.
- M-CSF mRNA and protein levels were assessed after TNF-α stimulation, with and without NF-κB inhibition (BAY 11-7082).
Main Results:
- P.e-LPS significantly increased TNF-α mRNA expression in a dose-dependent manner.
- TNF-α treatment dose-dependently upregulated M-CSF mRNA and protein expression.
- Inhibition of NF-κB signaling reduced TNF-α-induced M-CSF protein expression.
Conclusions:
- P. endodontalis LPS induces TNF-α mRNA expression in osteoblasts.
- TNF-α likely induces M-CSF expression in osteoblasts via NF-κB signaling.
- This suggests an autocrine mechanism for bone destruction in P.e-LPS-induced periodontitis.
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