Heterogeneous Expression of Toll-like Receptor 4 and Downregulation of Toll-like Receptor 4 Expression on Human Gingival Fibroblasts by Porphyromonas gingivalis Lipopolysaccharide

Porphyromonas gingivalis (P. gingivalis) is implicated in the initiation and progression of periodontitis. Human gingival fibroblasts (HGFs) are the major constituent of gingival connective tissue. P. gingivalis or its components such as lipopolysaccharide (LPS) upregulate the production of various...

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Veröffentlicht in:Biochemical and biophysical research communications 2001-11, Vol.288 (4), p.863-867
Hauptverfasser: Wang, Pao-Li, Oido-Mori, Mari, Fujii, Takeo, Kowashi, Yusuke, Kikuchi, Masanori, Suetsugu, Yasushi, Tanaka, Junzo, Azuma, Yasutaka, Shinohara, Mitsuko, Ohura, Kiyoshi
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container_issue 4
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container_title Biochemical and biophysical research communications
container_volume 288
creator Wang, Pao-Li
Oido-Mori, Mari
Fujii, Takeo
Kowashi, Yusuke
Kikuchi, Masanori
Suetsugu, Yasushi
Tanaka, Junzo
Azuma, Yasutaka
Shinohara, Mitsuko
Ohura, Kiyoshi
description Porphyromonas gingivalis (P. gingivalis) is implicated in the initiation and progression of periodontitis. Human gingival fibroblasts (HGFs) are the major constituent of gingival connective tissue. P. gingivalis or its components such as lipopolysaccharide (LPS) upregulate the production of various inflammatory cytokines including interleukin (IL)-1 and IL-6 in HGFs. Recently, we demonstrated that the binding of P. gingivalis LPS to Toll-like receptor 4 (TLR4) on HGFs activates various second messenger systems (Biochem. Biophys. Res. Commun. 273, 1161–1167, 2000). In the present study, we examined the level of TLR4 expression on HGFs by flow cytometric analysis (FACS), and studied the levels of IL-1 and IL-6 in the culture medium upon LPS stimulation of HGFs by enzyme-linked immunosorbent assay (ELISA). Upon stimulation by P. gingivalis LPS for 24 h, HGFs that expressed a high level of TLR4 secreted significantly higher levels of IL-1 and IL-6 than HGFs that expressed a low level of TLR4. On the other hand, after stimulation with P. gingivalis LPS for 24 h, the level of TLR4 on the surface of HGFs decreased. These results suggest that the level of TLR4 expression on HGFs reflects the extent of inflammation in the gingival tissue, and that P. gingivalis LPS downregulates TLR4 expression on HGFs. These findings may be used to control inflammatory and immune responses in periodontal disease.
doi_str_mv 10.1006/bbrc.2001.5842
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Human gingival fibroblasts (HGFs) are the major constituent of gingival connective tissue. P. gingivalis or its components such as lipopolysaccharide (LPS) upregulate the production of various inflammatory cytokines including interleukin (IL)-1 and IL-6 in HGFs. Recently, we demonstrated that the binding of P. gingivalis LPS to Toll-like receptor 4 (TLR4) on HGFs activates various second messenger systems (Biochem. Biophys. Res. Commun. 273, 1161–1167, 2000). In the present study, we examined the level of TLR4 expression on HGFs by flow cytometric analysis (FACS), and studied the levels of IL-1 and IL-6 in the culture medium upon LPS stimulation of HGFs by enzyme-linked immunosorbent assay (ELISA). Upon stimulation by P. gingivalis LPS for 24 h, HGFs that expressed a high level of TLR4 secreted significantly higher levels of IL-1 and IL-6 than HGFs that expressed a low level of TLR4. On the other hand, after stimulation with P. gingivalis LPS for 24 h, the level of TLR4 on the surface of HGFs decreased. These results suggest that the level of TLR4 expression on HGFs reflects the extent of inflammation in the gingival tissue, and that P. gingivalis LPS downregulates TLR4 expression on HGFs. 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Human gingival fibroblasts (HGFs) are the major constituent of gingival connective tissue. P. gingivalis or its components such as lipopolysaccharide (LPS) upregulate the production of various inflammatory cytokines including interleukin (IL)-1 and IL-6 in HGFs. Recently, we demonstrated that the binding of P. gingivalis LPS to Toll-like receptor 4 (TLR4) on HGFs activates various second messenger systems (Biochem. Biophys. Res. Commun. 273, 1161–1167, 2000). In the present study, we examined the level of TLR4 expression on HGFs by flow cytometric analysis (FACS), and studied the levels of IL-1 and IL-6 in the culture medium upon LPS stimulation of HGFs by enzyme-linked immunosorbent assay (ELISA). Upon stimulation by P. gingivalis LPS for 24 h, HGFs that expressed a high level of TLR4 secreted significantly higher levels of IL-1 and IL-6 than HGFs that expressed a low level of TLR4. 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Human gingival fibroblasts (HGFs) are the major constituent of gingival connective tissue. P. gingivalis or its components such as lipopolysaccharide (LPS) upregulate the production of various inflammatory cytokines including interleukin (IL)-1 and IL-6 in HGFs. Recently, we demonstrated that the binding of P. gingivalis LPS to Toll-like receptor 4 (TLR4) on HGFs activates various second messenger systems (Biochem. Biophys. Res. Commun. 273, 1161–1167, 2000). In the present study, we examined the level of TLR4 expression on HGFs by flow cytometric analysis (FACS), and studied the levels of IL-1 and IL-6 in the culture medium upon LPS stimulation of HGFs by enzyme-linked immunosorbent assay (ELISA). Upon stimulation by P. gingivalis LPS for 24 h, HGFs that expressed a high level of TLR4 secreted significantly higher levels of IL-1 and IL-6 than HGFs that expressed a low level of TLR4. On the other hand, after stimulation with P. gingivalis LPS for 24 h, the level of TLR4 on the surface of HGFs decreased. These results suggest that the level of TLR4 expression on HGFs reflects the extent of inflammation in the gingival tissue, and that P. gingivalis LPS downregulates TLR4 expression on HGFs. These findings may be used to control inflammatory and immune responses in periodontal disease.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>11688988</pmid><doi>10.1006/bbrc.2001.5842</doi><tpages>5</tpages></addata></record>
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ispartof Biochemical and biophysical research communications, 2001-11, Vol.288 (4), p.863-867
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subjects Antibodies, Monoclonal - immunology
Antibodies, Monoclonal - pharmacology
Cells, Cultured
Down-Regulation - drug effects
Drosophila Proteins
Enzyme-Linked Immunosorbent Assay
Fibroblasts - drug effects
Fibroblasts - metabolism
Fibroblasts - secretion
Flow Cytometry
Gingiva - cytology
Gingiva - drug effects
Gingiva - metabolism
Gingiva - secretion
Humans
Interleukin-1 - secretion
Interleukin-6 - secretion
Lipopolysaccharides - antagonists & inhibitors
Lipopolysaccharides - pharmacology
Membrane Glycoproteins - antagonists & inhibitors
Membrane Glycoproteins - immunology
Membrane Glycoproteins - metabolism
Porphyromonas gingivalis
Receptors, Cell Surface - antagonists & inhibitors
Receptors, Cell Surface - immunology
Receptors, Cell Surface - metabolism
Time Factors
Toll-Like Receptor 4
Toll-Like Receptors
title Heterogeneous Expression of Toll-like Receptor 4 and Downregulation of Toll-like Receptor 4 Expression on Human Gingival Fibroblasts by Porphyromonas gingivalis Lipopolysaccharide
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