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Activation of NLRP3 inflammasome in dendritic cells and macrophages by Mycoplasma salivarium

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Please use this identifier to cite or link to this item:https://doi.org/10.14943/doctoral.k11729
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Title: Activation of NLRP3 inflammasome in dendritic cells and macrophages by Mycoplasma salivarium
Other Titles: Mycoplasma salivariumによる樹状細胞ならびにマクロファージにおけるNLRP3インフラマソーム活性化
Authors: 杉山, 正博1 Browse this author
Authors(alt): Kang, Sung-Sik1
Issue Date: 25-Mar-2015
Abstract: The proinflammatory cytokine IL-1β plays crucial roles in the pathogenesis ofperiodontal disease. IL-1β is produced after processing of pro-IL-1β by caspase-1,which is activated by the multiprotein complex consisting of NLR, an adaptor proteinand procaspase-1, called an the inflammasome. Mycoplasma salivarium, human oralmicrobial flora, preferentially inhabits the gingival sulcus and is considered to play anetiological role in periodontal diseases. As a first step to clarify the etiological role ofthe organism in periodontal diseases, this study was designed to clarify whether itinduces production of IL-1β by innate immune cells such as dendritic cells ormacrophages by using M. pneumoniae, which is known to induce production of IL-1βby human macrophages, as a positive control.It was found that both live and heat-killed cells of M. salivarium induced productionof IL-1β by the murine dendritic cell line XS106 cells and also necrotic cell death calledpyroptosis in the cells. The activity was significantly and partially downregulated bysilencing of caspase-1 and NLRP3, respectively. BMMs from wild-type and NLRP3-,ASC- and caspase-1-deficient mice were examined for IL-1β production in response tothe mycoplasma. Live cells of M. salivarium almost completely lost the activity toinduce IL-1β production by macrophages derived from ASC- and caspase-1-deficientmice. In addition, the activity toward BMMs from NLRP3-deficient mice wassignificantly but not completely attenuated. These results suggest that live cells of M.salivarium are able to activate several types of inflammasome, including the NLRP3inflammasome, to produce IL-1β.Taken together, the results of this study suggests that M. salivarium plays anetiological role in periodontal diseases through induction of inflammatory IL-1βproduction by dendritic cells and macrophages that have infiltrated inflamed gingivalconnective tissue.
Conffering University: 北海道大学
Degree Report Number: 甲第11729号
Degree Level: 博士
Degree Discipline: 歯学
Examination Committee Members: (主査) 教授 北川 善政, 教授 柴田 健一郎, 教授 田村 正人
Degree Affiliation: 歯学研究科(口腔医学専攻)
Type: theses (doctoral)
URI: http://hdl.handle.net/2115/60276
Appears in Collections:学位論文 (Theses) > 博士 (歯学)
課程博士 (Doctorate by way of Advanced Course) > 歯学院(Graduate School of Dental Medicine)

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