Interleukin-17A Stimulates Migration of Periodontal Ligament Fibroblasts Via p38 MAPK/NF-κB -Dependent MMP-1 Expression

被引:32
作者
Wu, Yan
Zhu, Lingxin
Liu, Lingshuang
Zhang, Jie
Peng, Bin [1 ,2 ]
机构
[1] Wuhan Univ, State Key Lab Breeding Base Basic Sci Stomatol Hu, Sch & Hosp Stomatol, Wuhan 430079, Peoples R China
[2] Wuhan Univ, Key Lab Oral Biomed Minist Educ, Sch & Hosp Stomatol, Wuhan 430079, Peoples R China
基金
中国国家自然科学基金;
关键词
MATRIX METALLOPROTEINASES; I COLLAGEN; INFLAMMATORY CYTOKINE; PLATELET-RICH; CELLS; PROLIFERATION; INVOLVEMENT; REGULATORS; SECRETION; BIOLOGY;
D O I
10.1002/jcp.24444
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Interleukin-17 (IL-17) is a cytokine secreted predominantly by Th17 cells. Although IL-17 is primarily associated with the induction of tissue inflammation, the other biological functions of IL-17, including its wound-healing functions, have yet to be thoroughly explored. Fibroblast proliferation and migration play essential roles in periodontal wound-healing responses. In this study, we report that IL-17A can increase the migration and expression of matrix metalloproteinase (MMP)-1 in human periodontal ligament (PDL) fibroblasts but has no effect on PDL fibroblast proliferation. IL-17A-induced MMP-1 expression led to cell migration, which was attenuated by pre-treatment with IL-17 receptor neutralizing antibody and small interfering RNA (siRNA) for MMP-1. The IL-17A-induced cell migration was also attenuated by its tissue inhibitor of matrix metalloproteinase (TIMP)-1. In addition, a p38 mitogen-activated protein kinase (MAPK) inhibitor (SB203580) inhibited IL-17A-induced increase of the migration and MMP-1 upregulation of PDL fibroblasts. The involvement of p38 MAPK in IL-17A-induced MMP-1 expression and cell migration was further confirmed by transfection of p38 siRNA. A nuclear factor kappaB (NF-B) inhibitor (pyrrolidine dithiocarbamate) also suppressed the cell migration and MMP-1 expression enhanced by IL-17A. Moreover, transfection with p38 siRNA inhibited IL-17A-induced NF-B nuclear translocation as well as NF-B binding activity. Our results suggest that IL-17A enhances the migration of PDL fibroblasts by increasing MMP-1 expression through the IL-17 receptor, p38 MAPK, and NF-B signal transduction pathways. J. Cell. Physiol. 229: 292-299, 2014. (c) 2013 Wiley Periodicals, Inc.
引用
收藏
页码:292 / 299
页数:8
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