Browsing by Author "HEEKE, K.S."

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    INTERACTIONS OF HUMAN ORAL CELLS WITH ORAL BACTERIAL
    (Office of the Vice Chancellor for Research, 2012-04-13) HEEKE, K.S.; GREGORY, R.L.; SONG, F.; WINDSOR, L.J.
    Introduction: Streptococcus mutans is the main etiological cause of den-tal caries, and it has been shown that individuals who smoke have increased dental caries. S. mutans is known to bind to or interact with MG63 osteo-blasts. However, very little is known about the effects of tobacco directly on these bacteria on their ability to affect human pulp MG63 osteoblasts. We are hypothesizing that tobacco upregulates the expression of pro-inflammatory cytokines and MMPs to increase the pathogenic potential of S. mutans. The objective of this research project is to investigate the effects that nicotine, cigarette smoke condensate (CSC), and dissolvable smokeless tobacco (DST)-extract treated bacterial cells have on humanMG63 osteo-blasts, in respect to their release of pro-inflammatory and anti-inflammatory cytokines, as well as MMP expression. In addition, the effects of the S. mutans cells will be examined for the ability to affect MG63 osteoblast growth. The long-term goal is to develop treatment modalities to reduce the effects of smoking on dental caries. Materials and Methods: S. mutans UA159 was incubated in Tryptic Soy Broth (TSB), with the following concentrations: 2 mg/mL nicotine, 0.125 mg/mL CSC, 100 uL/3 mL DST-extract, and a 0 mg/mL control group. The cultures were grown in the presence of the tobacco products for 8 h at 37oC in 5% CO2, and centrifuged to isolate cells and supernatants. The cells were washed and heat-killed for 1 h at 60oC. Human MG63 osteoblasts were iso-lated from extracted teeth, and cell passages 3-8 will be used. The tobacco-treated S. mutans cells and supernatants will be incubated with the osteo-blasts in culture plates for 72 h and cytokine expression evaluated by re-verse transcriptase polymerase chain reaction. Results: The protein concentration of each tobacco-treated sample was found. The undiluted concentrations of the nicotine- and CSC-treated cells were slightly lower and the DST-treated cells was slightly higher than the control cells. The undiluted nicotine (p<0.05) and DST-treated supernatants were higher than the control, while the CSC supernatant protein concentra-tion was lower. From our previous studies, it was found that nicotine in-creases bacteriocin production of S. mutans, so we might hypothesize that nicotine induces bacteriocin secretion, thus increasing dental caries.