Effect of globular adiponectin on interleukin-6 and interleukin-8 expression in periodontal ligament and gingival fibroblasts

被引:9
作者
Park, Hong Gyu [1 ]
Bak, Eun Jung [2 ]
Kim, Ji Hye [1 ,3 ,4 ]
Lee, Yang-Sin [1 ]
Choi, Seong-Ho [3 ,5 ]
Cha, Jeong-Heon [1 ,2 ,3 ,4 ]
Yoo, Yun-Jung [1 ,3 ,4 ]
机构
[1] Yonsei Univ, Coll Dent, Oral Sci Res Ctr, Project BK21,Dept Oral Biol, Seoul 120752, South Korea
[2] Yonsei Univ, Coll Dent, Oral Sci Res Ctr, Seoul 120752, South Korea
[3] Yonsei Univ, Coll Dent, Res Ctr Orofacial Hard Tissue Regenerat, Seoul 120752, South Korea
[4] Yonsei Univ, Grad Sch, Dept Appl Life Sci, Seoul 120752, South Korea
[5] Yonsei Univ, Coll Dent, Res Inst Periodontal Regenerat, Dept Periodontol, Seoul 120752, South Korea
基金
新加坡国家研究基金会;
关键词
Adiponectin; Periodontal ligament; Fibroblasts; Receptors; Cytokines;
D O I
10.5051/jpis.2011.41.3.149
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Purpose: Globular adiponectin (gAd) is a type of adipocytokine, which is mainly produced by adipose tissue. It has been reported that gAd acts as a pro-as well as an anti-inflammatory factor. Interleukin (IL)-6 and IL-8 are pro-inflammatory cytokines. To investigate the role of gAd on periodontal tissues, the expression of adiponectin receptor 1 (AdipoR1) and the effect of gAd on the expression of IL-6 and IL-8 were investigated in periodontal ligament (PDL) and gingival fibroblasts. Methods: PDL and gingival fibroblasts were cultured from human periodontal tissues. gAd derived from Escherichia coli and murine myeloma cells were used. The expression of AdipoR1 was estimated by reverse transcription-polymerase chain reaction and western blot. The expression of cytokines was measured by enzyme-linked immunosorbent assay. Results: PDL and gingival fibroblasts expressed both mRNA and protein of AdipoR1. gAd derived from E. coli increased the production of IL-6 and IL-8, but polymyxin B, an inhibitor of lipopolysaccharide (LPS), inhibited IL-6 and IL-8 production induced by gAd in both types of cells. gAd derived from murine myeloma cells did not induce IL-6 and IL-8 production in those cells. gAd derived from E. coli contained higher levels of LPS than gAd derived from murine myeloma cells. LPS increased production of IL-6 and IL-8 in PDL and gingival fibroblasts, but pretreatment of cells with gAd derived from murine myeloma cells did not inhibit LPS-induced IL-6 and IL-8 expression. Conclusions: Our results suggest that PDL and gingival fibroblasts express AdipoR1 and that gAd does not act as a modulator of IL-6 and IL-8 expression in PDL and gingival fibroblasts.
引用
收藏
页码:149 / 156
页数:8
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