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Updated: Dec 7, 2025

Isolation, Processing and Analysis of Murine Gingival Cells
Published on: July 2, 2013
Activation of Gingival Fibroblasts by Bacterial Cyclic Dinucleotides and Lipopolysaccharide
Samira Elmanfi1, Herman O Sintim2, Jie Zhou2
1Department of Periodontology, Institute of Dentistry, University of Turku, 20520 Turku, Finland.
Abstract:
Human gingival fibroblasts (HGFs) recognize microbe-associated molecular patterns (MAMPs) and respond with inflammatory proteins. Simultaneous impacts of bacterial cyclic di-guanosine monophosphate (c-di-GMP), cyclic di-adenosine monophosphate (c-di-AMP), and lipopolysaccharide (LPS) on gingival keratinocytes have been previously demonstrated, but the effects of these MAMPs on other periodontal cell types, such as gingival fibroblasts, remain to be clarified. The present aim was to examine the independent and combined effects of these cyclic dinucleotides and LPS on interleukin (IL) and matrix metalloproteinase (MMP) response of HGFs. The cells were incubated with c-di-GMP and c-di-AMP, either in the presence or absence of Porphyromonas gingivalis LPS, for 2 h and 24 h. The levels of IL-8, -10, and -34, and MMP-1, -2, and -3 secreted were measured by the Luminex technique. LPS alone or together with cyclic dinucleotides elevated IL-8 levels. IL-10 levels were significantly increased in the presence of c-di-GMP and LPS after 2 h but disappeared after 24 h of incubation. Concurrent treatment of c-di-AMP and LPS elevated MMP-1 levels, whereas c-di-GMP with LPS suppressed MMP-2 levels but increased MMP-3 levels. To conclude, we produce evidence that cyclic dinucleotides interact with LPS-mediated early response of gingival fibroblasts, while late cellular response is mainly regulated by LPS.
Insights
Bacterial cyclic dinucleotides modulate human gingival fibroblast responses to lipopolysaccharide (LPS). While early inflammatory protein release is influenced by both, later responses are primarily driven by LPS.
Area of Science:
- Oral biology and immunology
- Periodontal disease mechanisms
- Cellular responses to microbial stimuli
Background:
- Human gingival fibroblasts (HGFs) are key cells in periodontal tissues.
- Microbe-associated molecular patterns (MAMPs), including cyclic dinucleotides and lipopolysaccharide (LPS), trigger inflammatory responses.
- The combined effects of cyclic dinucleotides and LPS on HGFs are not fully understood.
Purpose of the Study:
- To investigate the independent and combined effects of cyclic di-guanosine monophosphate (c-di-GMP), cyclic di-adenosine monophosphate (c-di-AMP), and Porphyromonas gingivalis LPS on HGFs.
- To analyze the secretion of interleukin (IL) and matrix metalloproteinase (MMP) by HGFs under these conditions.
Main Methods:
- HGFs were incubated with c-di-GMP and c-di-AMP, with or without P. gingivalis LPS, for 2 and 24 hours.
- Secreted levels of IL-8, IL-10, IL-34, MMP-1, MMP-2, and MMP-3 were quantified using the Luminex technique.
Main Results:
- LPS, alone or with cyclic dinucleotides, increased IL-8 levels.
- IL-10 increased with c-di-GMP and LPS at 2 hours but not at 24 hours.
- c-di-AMP and LPS elevated MMP-1; c-di-GMP and LPS suppressed MMP-2 but increased MMP-3.
Conclusions:
- Cyclic dinucleotides interact with LPS to modulate the early inflammatory response of HGFs.
- The late-stage cellular response of HGFs to these MAMPs is predominantly regulated by LPS.
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