Journal of Oral Science Research ›› 2023, Vol. 39 ›› Issue (6): 534-540.DOI: 10.13701/j.cnki.kqyxyj.2023.06.013

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Effects of Escherichia Coli Lipopolysaccharide on Biological Behaviors of Rat Dental Follicle Stem Cells

JIANG Zhen, YAN Yanhong, HAN Xue, JIANG Beizhan*   

  1. Department of Pediatrics, School and Hospital of Stomatology, Tongji University, Shanghai Engineering Research Center of Tooth Restoration and Regeneration, Shanghai 200072, China
  • Received:2022-12-01 Online:2023-06-28 Published:2023-06-21

Abstract: Objective: To investigate the effects of Escherichia coli lipopolysaccharide (E. coli LPS) on biological behaviors of rat dental follicle stem cells (rDFSCs). Methods: rDFSCs were cultured and identified, and then were treated with different concentrations of E. coli LPS (0, 1, 10 μg/mL). The mRNA levels of pro-inflammatory genes were measured by quantitative real-time fluorescence polymerase chain reaction (qRT-PCR). The effects of LPS on proliferation and migration ability of rDFSCs were assessed by CCK-8 and scratch test plus transwell assay, respectively. The osteogenic capability of rDFSCs was detected by alkaline phosphatase (ALP) staining and alizarin red staining, and their osteogenic-related gene mRNA levels were measured by qRT-PCR. Results: The gene expressions of IL-6, IL-1 β, and TNF-α were significantly upregulated under 1 or 10 μg/mL LPS treatment (P<0.05). LPS at 1 μg/mL significantly promoted the proliferation and migration of rDFSCs (P<0.05), while a higher concentration (10 μg/mL) did not show any improvement. ALP staining intensity and the number of mineralized nodules decreased, and the expressions of osteogenic markers RUNX2, COL1, and OPN were inhibited in LPS-treated group (P<0.05).Conclusion: The osteogenic ability of rDFSCs was significantly inhibited under inflammatory microenvironment simulated by E.coli LPS, and LPS promoted the proliferation and migration of rDFSCs at low concentration.

Key words: lipopolysaccharide, dental follicle stem cells, cell proliferation, cell migration, osteogenic differentiation