201. [Expression of triggering receptors expressed on myeloid-1 in innate response to Porphyromonas gingivalis in macrophages]
- Author
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Lang, Lei, Hou-xuan, Li, Sheng-bo, Pan, and Fu-hua, Yan
- Subjects
Mice, Inbred C57BL ,Mice ,Membrane Glycoproteins ,Interleukin-6 ,Tumor Necrosis Factor-alpha ,Macrophages, Peritoneal ,Animals ,Receptors, Immunologic ,Peptides ,Porphyromonas gingivalis ,Cells, Cultured ,Triggering Receptor Expressed on Myeloid Cells-1 ,Up-Regulation - Abstract
To investigate the role of triggering receptors expressed on myeloid-1(TREM-1) in innate response to Porphyromonas gingivalis(Pg) in mice macrophages and its potential role in periodontitis development.Peritoneal macrophages from mice were harvested, separated and cultured, then challenged with viable Pg. Transcription and protein expression in macrophages were assessed with real time PCR and flow cytometry respectively.LP-17 peptide (10, 100 and 1000 µg/L) was utilized to block TREM-1, and tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6) were detected by enzyme linked absorbent analysis.At 2 h after Pg challenge, transcription of TREM-1 was significantly up-regulated after Pg challenge[(7.99 ± 1.11) fold vs blank]. At 24 h after bacteria infection, increased TREM-1 expression was demonstrated by flow cytometry, with mean fluorescent intensity increasing from (7.05 ± 1.85) in blank group to (13.17 ± 2.33) in experimental group. Proinflammatory cytokine (TNF-α and IL-6) production was significantly decreased after blocking TREM-1 by LP-17 peptide(100 and 1000 µg/L).TREM-1 enhanced innate immune response to Pg in macrophages, which may facilitate periodontitis development.
- Published
- 2014