Brain-Derived Neurotrophic Factor Inhibits Peptidoglycan-Induced Inflammatory Cytokine Expression in Human Dental Pulp Cells

被引:7
作者
Takeda, Katsuhiro [1 ]
Tokunaga, Naoko [1 ]
Aida, Yusuke [1 ]
Kajiya, Mikihito [1 ]
Ouhara, Kazuhisa [1 ]
Sasaki, Shinya [1 ]
Mizuno, Noriyoshi [1 ]
Fujita, Tsuyoshi [1 ]
Kurihara, Hidemi [1 ]
机构
[1] Hiroshima Univ, Inst Biomed & Hlth Sci, Div Appl Life Sci, Dept Periodontal Med, Hiroshima, Japan
关键词
brain-derived neurotrophic factor; peptidoglycan; pulp cells; endodontic treatment; VASCULAR ENDOTHELIAL-CELLS; GENE-EXPRESSION; RECEPTORS; FAMILY; FIBROBLASTS; BDNF; TRKB;
D O I
10.1007/s10753-016-0474-4
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The aim of this study was to examine the anti-inflammatory effect of brain-derived neurotrophic factor (BDNF) on human dental pulp cells (HDPCs) and identify the intracellular signaling pathway involved. We investigated the effect of BDNF (50 ng/ml) on interleukin (IL)-6 and IL-8 expression in peptidoglycan (PGN)-treated HDPCs. An inhibition assay was performed with MAPK or NF-kappa B inhibitors to determine the possible signaling pathway. IL-6 and IL-8 mRNA, IL-6 and IL-8 protein, and phosphorylated p38 kinase activity were determined using real-time PCR, ELISA, and Western blot analysis, respectively. BDNF significantly attenuated PGN-induced IL-6 and IL-8 mRNA and protein levels in HDPCs. A p38 inhibitor also inhibited IL-6 and IL-8 mRNA transcription. PGN stimulated phosphorylated p38 kinase activity in HDPCs, which was inhibited by BDNF. Suppression of phosphorylated p38 kinase activity by BDNF in HDPCs inhibited increased IL-6 and IL-8 expression induced by PGN. Our findings suggest that BDNF regulates intracellular signaling molecule activities to exert its anti-inflammatory effect.
引用
收藏
页码:240 / 247
页数:8
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