Porphyromonas gingivalis lipopolysaccharides regulate functions of bone marrow mesenchymal stem cells

被引:41
|
作者
Tang, J. [1 ,2 ,3 ,4 ]
Wu, T. [5 ]
Xiong, J. [3 ,4 ]
Su, Y. [5 ]
Zhang, C. [5 ]
Wang, S. [5 ,6 ]
Tang, Z. [2 ]
Liu, Y. [3 ,4 ]
机构
[1] Cent South Univ, Xiangya Hosp, Dept Oral & Maxillofacial Surg, Changsha 410008, Hunan, Peoples R China
[2] Cent South Univ, Xiangya Stomatol Hosp, Dept Oral & Maxillofacial Surg, Changsha 410008, Hunan, Peoples R China
[3] Capital Med Univ, Sch Stomatol, Lab Tissue Regenerat & Immunol, Beijing Key Lab Tooth Regenerat & Funct Reconstru, Beijing 100050, Peoples R China
[4] Capital Med Univ, Sch Stomatol, Dept Periodont, Beijing Key Lab Tooth Regenerat & Funct Reconstru, Beijing 100050, Peoples R China
[5] Capital Med Univ, Sch Stomatol, Salivary Gland Dis Ctr & Mol Lab Gene Therapy & T, Beijing Key Lab Tooth Regenerat & Funct Reconstru, Beijing 100050, Peoples R China
[6] Capital Med Univ, Sch Basic Med Sci, Dept Biochem & Mol Biol, Beijing 100050, Peoples R China
基金
中国国家自然科学基金;
关键词
OSTEOGENIC DIFFERENTIATION; INFLAMMATORY CYTOKINE; TISSUE REGENERATION; T-CELLS; PERIODONTITIS; POTENCY;
D O I
10.1111/cpr.12173
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
ObjectivesPeriodontitis is one of the most widespread inflammatory diseases; it causes tooth loss and is also associated with a variety of systemic diseases. Mesenchymal stem cells (MSCs) have been used to treat periodontitis. However, it is unknown whether bacterial toxins in the periodontal environment affect MSC-mediated periodontal regeneration. Porphyromonas gingivalis lipopolysaccharides (Pg-LPS) are key toxins for development of periodontitis. The purpose of the present study was to investigate effects of P.gingivalis LPS on biological properties of MSCs. Materials and methodsMesenchymal stem cells from bone marrow (BMMSCs) were treated with different concentrations of P.gingivalis LPS (0.1-10g/ml), then its effects were evaluated on biological properties of BMMSCs including proliferation, apoptosis, osteogenic differentiation and capacities to inhibit activated T cells. ResultsLow concentration of P.gingivalis LPS (0.1g/ml) accelerated MSC proliferation, osteogenic differentiation and capacities to inhibit activated T cells via up-regulation of nitric oxide. However, high concentration of P.gingivalis LPS (10g/ml) reduced MSC proliferation, osteogenic differentiation and capacities to inhibit activated T cells. ConclusionsMesenchymal stem cells were functionally different following exposure to P.gingivalis LPS at the investigated concentrations. These findings suggest that MSC-mediated periodontal regeneration may be regulated by P.gingivalis LPS.
引用
收藏
页码:239 / 248
页数:10
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