4.7 Article

Porphyromonas gingivalis lipopolysaccharides regulate functions of bone marrow mesenchymal stem cells

Journal

CELL PROLIFERATION
Volume 48, Issue 2, Pages 239-248

Publisher

WILEY
DOI: 10.1111/cpr.12173

Keywords

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Categories

Funding

  1. Beijing Municipal Committee for Science and Technology [Z121100005212004]
  2. National Basic Research Program of China [2010CB944801]
  3. Funding Project for Academic Human Resources Development in Institutions of Higher Learning Under the Jurisdiction of Beijing Municipality [PHR20090510]
  4. Funding Project to Science Facility in Institutions of Higher Learning Under the Jurisdiction of Beijing Municipality [PXM 2009-014226-074691]
  5. National Natural Science Foundation of China [81222011, 81300892]
  6. Science and Technology Activities of Beijing Overseas Students Preferred Foundation
  7. Beijing Key Laboratory Foundation of Science and Technology Special Work [Z121107002812034]

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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.

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