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Lipopolysaccharide induces rapid loss of follicular dendritic cell‐secreted protein in the junctional epithelium
Author(s) -
Oshiro A.,
Iseki S.,
Miyauchi M.,
Terashima T.,
Kawaguchi Y.,
Ikeda Y.,
Shinomura T.
Publication year - 2012
Publication title -
journal of periodontal research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.31
H-Index - 83
eISSN - 1600-0765
pISSN - 0022-3484
DOI - 10.1111/j.1600-0765.2012.01482.x
Subject(s) - junctional epithelium , epithelium , lipopolysaccharide , microbiology and biotechnology , follicular dendritic cells , biology , respiratory epithelium , inflammation , innate immune system , chemistry , immunology , immune system , t cell , genetics , antigen presenting cell
Oshiro A, Iseki S, Miyauchi M, Terashima T, Kawaguchi Y, Ikeda Y, Shinomura T. Lipopolysaccharide induces rapid loss of follicular dendritic cell‐secreted protein in the junctional epithelium. J Periodont Res 2012; 47: 689–694. © 2012 John Wiley & Sons A/S Background and Objective:  We have previously reported that mRNA encoding follicular dendritic cell‐secreted protein (FDC‐SP) is expressed specifically in the junctional epithelium at the gingival crevice. Other tissues, such as tonsil, prostate gland and trachea, also express high levels of FDC‐SP. These tissues participate in a range of functions closely related to innate immunity. Therefore, it is hypothesized that FDC‐SP plays a crucial role in close association with the host defense system within the gingival crevice. Accordingly, the main aim of this study was to investigate the expression and localization of FDC‐SP in and around the junctional epithelium and to observe the dynamic changes of FDC‐SP in experimental inflammation. Material and Methods:  We examined, immunohistochemically, the expression of FDC‐SP in the junctional epithelium using a specific antibody raised in rabbit after immunization with a synthetic peptide derived from the hydrophilic region of FDC‐SP. Experimental inflammation was induced in the upper molars of Wistar rats by applying bacterial lipopolysaccharide (LPS; 5 mg/mL in sterile saline) for 1 h. Results:  We confirmed that FDC‐SP is present in the junctional epithelium in a pattern that is consistent with the expression of FDC‐SP mRNA. Of special interest is that no FDC‐SP was detectable in the junctional epithelium 3 h after transient topical treatment with LPS. Conclusion:  The presence of FDC‐SP in the junctional epithelium and its loss after LPS treatment strongly support our hypothesis of FDC‐SP playing a crucial role in close association with the host defense system within the gingival crevice.

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