Inducible expression of A Disintegrin and Metalloproteinase 8 in chronic periodontitis and gingival epithelial cells

Background and Objectives The expression of A Disintegrin and Metalloproteinase 8 (ADAM8) is associated with several inflammatory diseases. Elevated ADAM8 levels have been shown in gingival crevicular fluid of patients with chronic periodontitis. The objective of this study was to investigate ADAM8...

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Veröffentlicht in:Journal of periodontal research 2017-06, Vol.52 (3), p.582-593
Hauptverfasser: Aung, W. P. P., Chotjumlong, P., Pata, S., Montreekachon, P., Supanchart, C., Khongkhunthian, S., Sastraruji, T., Krisanaprakornkit, S.
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container_end_page 593
container_issue 3
container_start_page 582
container_title Journal of periodontal research
container_volume 52
creator Aung, W. P. P.
Chotjumlong, P.
Pata, S.
Montreekachon, P.
Supanchart, C.
Khongkhunthian, S.
Sastraruji, T.
Krisanaprakornkit, S.
description Background and Objectives The expression of A Disintegrin and Metalloproteinase 8 (ADAM8) is associated with several inflammatory diseases. Elevated ADAM8 levels have been shown in gingival crevicular fluid of patients with chronic periodontitis. The objective of this study was to investigate ADAM8 expression in chronic periodontitis tissues compared with that in normal tissues. ADAM8 expression and its inductive mechanism were examined in human gingival epithelial cells (HGECs) and human gingival fibroblasts. Material and Methods Total RNA and protein were extracted from gingival biopsies of 33 patients with chronic periodontitis and those of 23 healthy volunteers. ADAM8 mRNA and protein expression was analyzed by real‐time polymerase chain reaction, immunoblotting and immunohistochemistry. ADAM8 expression in control and stimulated cells in the presence or absence of specific inhibitors for mitogen‐activated protein kinase pathways was assayed by real‐time polymerase chain reaction, immunoblotting, flow cytometry and immunofluorescence. Results ADAM8 mRNA and protein expression in chronic periodontitis tissues was significantly greater than that in normal tissues (p < 0.01). Significantly increased ADAM8 expression was detected in the gingival epithelium of chronic periodontitis tissues (p < 0.001). ADAM8 mRNA expression in HGECs, but not in human gingival fibroblasts, was significantly induced by stimulation with Fusobacterium nucleatum (p < 0.05), partially via the p44/42 mitogen‐activated protein kinase pathway. ADAM8 expression in the cell lysates and on the surface of HGECs was induced by stimulation with F. nucleatum. Conclusion ADAM8 expression is increased in inflamed chronic periodontitis tissues and localized within gingival epithelium, consistent with an upregulation of ADAM8 expression in F. nucleatum‐stimulated HGECs, suggesting a possible role of ADAM8 in innate immunity of periodontal tissue.
doi_str_mv 10.1111/jre.12426
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P. P. ; Chotjumlong, P. ; Pata, S. ; Montreekachon, P. ; Supanchart, C. ; Khongkhunthian, S. ; Sastraruji, T. ; Krisanaprakornkit, S.</creator><creatorcontrib>Aung, W. P. P. ; Chotjumlong, P. ; Pata, S. ; Montreekachon, P. ; Supanchart, C. ; Khongkhunthian, S. ; Sastraruji, T. ; Krisanaprakornkit, S.</creatorcontrib><description>Background and Objectives The expression of A Disintegrin and Metalloproteinase 8 (ADAM8) is associated with several inflammatory diseases. Elevated ADAM8 levels have been shown in gingival crevicular fluid of patients with chronic periodontitis. The objective of this study was to investigate ADAM8 expression in chronic periodontitis tissues compared with that in normal tissues. ADAM8 expression and its inductive mechanism were examined in human gingival epithelial cells (HGECs) and human gingival fibroblasts. Material and Methods Total RNA and protein were extracted from gingival biopsies of 33 patients with chronic periodontitis and those of 23 healthy volunteers. ADAM8 mRNA and protein expression was analyzed by real‐time polymerase chain reaction, immunoblotting and immunohistochemistry. ADAM8 expression in control and stimulated cells in the presence or absence of specific inhibitors for mitogen‐activated protein kinase pathways was assayed by real‐time polymerase chain reaction, immunoblotting, flow cytometry and immunofluorescence. Results ADAM8 mRNA and protein expression in chronic periodontitis tissues was significantly greater than that in normal tissues (p &lt; 0.01). Significantly increased ADAM8 expression was detected in the gingival epithelium of chronic periodontitis tissues (p &lt; 0.001). ADAM8 mRNA expression in HGECs, but not in human gingival fibroblasts, was significantly induced by stimulation with Fusobacterium nucleatum (p &lt; 0.05), partially via the p44/42 mitogen‐activated protein kinase pathway. ADAM8 expression in the cell lysates and on the surface of HGECs was induced by stimulation with F. nucleatum. Conclusion ADAM8 expression is increased in inflamed chronic periodontitis tissues and localized within gingival epithelium, consistent with an upregulation of ADAM8 expression in F. nucleatum‐stimulated HGECs, suggesting a possible role of ADAM8 in innate immunity of periodontal tissue.</description><identifier>ISSN: 0022-3484</identifier><identifier>EISSN: 1600-0765</identifier><identifier>DOI: 10.1111/jre.12426</identifier><identifier>PMID: 27859260</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>A Disintegrin and Metalloproteinase 8 ; ADAM protein ; ADAM Proteins - metabolism ; ADAM8 protein ; Adult ; Blotting, Western ; Case-Control Studies ; chronic periodontitis ; Chronic Periodontitis - metabolism ; Dentistry ; Epithelial cells ; Epithelial Cells - metabolism ; Epithelium ; Fibroblasts ; Flow Cytometry ; Fluorescent Antibody Technique ; Fusobacterium nucleatum ; Gene expression ; Gingiva ; Gingiva - cytology ; Gingiva - metabolism ; Gum disease ; Humans ; Immunoblotting ; Immunofluorescence ; Immunohistochemistry ; Inflammatory diseases ; Innate immunity ; Kinases ; Lysates ; MAP kinase ; Matrix Metalloproteinase 8 - metabolism ; Membrane Proteins - metabolism ; Middle Aged ; Neutrophil collagenase ; Periodontitis ; Polymerase chain reaction ; Protein expression ; Protein kinase ; Proteins ; Real-Time Polymerase Chain Reaction ; Young Adult</subject><ispartof>Journal of periodontal research, 2017-06, Vol.52 (3), p.582-593</ispartof><rights>2016 John Wiley &amp; Sons A/S. Published by John Wiley &amp; Sons Ltd</rights><rights>2016 John Wiley &amp; Sons A/S. 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P. P.</creatorcontrib><creatorcontrib>Chotjumlong, P.</creatorcontrib><creatorcontrib>Pata, S.</creatorcontrib><creatorcontrib>Montreekachon, P.</creatorcontrib><creatorcontrib>Supanchart, C.</creatorcontrib><creatorcontrib>Khongkhunthian, S.</creatorcontrib><creatorcontrib>Sastraruji, T.</creatorcontrib><creatorcontrib>Krisanaprakornkit, S.</creatorcontrib><title>Inducible expression of A Disintegrin and Metalloproteinase 8 in chronic periodontitis and gingival epithelial cells</title><title>Journal of periodontal research</title><addtitle>J Periodontal Res</addtitle><description>Background and Objectives The expression of A Disintegrin and Metalloproteinase 8 (ADAM8) is associated with several inflammatory diseases. Elevated ADAM8 levels have been shown in gingival crevicular fluid of patients with chronic periodontitis. The objective of this study was to investigate ADAM8 expression in chronic periodontitis tissues compared with that in normal tissues. ADAM8 expression and its inductive mechanism were examined in human gingival epithelial cells (HGECs) and human gingival fibroblasts. Material and Methods Total RNA and protein were extracted from gingival biopsies of 33 patients with chronic periodontitis and those of 23 healthy volunteers. ADAM8 mRNA and protein expression was analyzed by real‐time polymerase chain reaction, immunoblotting and immunohistochemistry. ADAM8 expression in control and stimulated cells in the presence or absence of specific inhibitors for mitogen‐activated protein kinase pathways was assayed by real‐time polymerase chain reaction, immunoblotting, flow cytometry and immunofluorescence. Results ADAM8 mRNA and protein expression in chronic periodontitis tissues was significantly greater than that in normal tissues (p &lt; 0.01). Significantly increased ADAM8 expression was detected in the gingival epithelium of chronic periodontitis tissues (p &lt; 0.001). ADAM8 mRNA expression in HGECs, but not in human gingival fibroblasts, was significantly induced by stimulation with Fusobacterium nucleatum (p &lt; 0.05), partially via the p44/42 mitogen‐activated protein kinase pathway. ADAM8 expression in the cell lysates and on the surface of HGECs was induced by stimulation with F. nucleatum. 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P. P.</creator><creator>Chotjumlong, P.</creator><creator>Pata, S.</creator><creator>Montreekachon, P.</creator><creator>Supanchart, C.</creator><creator>Khongkhunthian, S.</creator><creator>Sastraruji, T.</creator><creator>Krisanaprakornkit, S.</creator><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>201706</creationdate><title>Inducible expression of A Disintegrin and Metalloproteinase 8 in chronic periodontitis and gingival epithelial cells</title><author>Aung, W. P. P. ; Chotjumlong, P. ; Pata, S. ; Montreekachon, P. ; Supanchart, C. ; Khongkhunthian, S. ; Sastraruji, T. ; Krisanaprakornkit, S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3866-a8ddacdcf33630059adba8e4053bc2d1c884cee2ff02ff28741fc8375ed230c73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>A Disintegrin and Metalloproteinase 8</topic><topic>ADAM protein</topic><topic>ADAM Proteins - metabolism</topic><topic>ADAM8 protein</topic><topic>Adult</topic><topic>Blotting, Western</topic><topic>Case-Control Studies</topic><topic>chronic periodontitis</topic><topic>Chronic Periodontitis - metabolism</topic><topic>Dentistry</topic><topic>Epithelial cells</topic><topic>Epithelial Cells - metabolism</topic><topic>Epithelium</topic><topic>Fibroblasts</topic><topic>Flow Cytometry</topic><topic>Fluorescent Antibody Technique</topic><topic>Fusobacterium nucleatum</topic><topic>Gene expression</topic><topic>Gingiva</topic><topic>Gingiva - cytology</topic><topic>Gingiva - metabolism</topic><topic>Gum disease</topic><topic>Humans</topic><topic>Immunoblotting</topic><topic>Immunofluorescence</topic><topic>Immunohistochemistry</topic><topic>Inflammatory diseases</topic><topic>Innate immunity</topic><topic>Kinases</topic><topic>Lysates</topic><topic>MAP kinase</topic><topic>Matrix Metalloproteinase 8 - metabolism</topic><topic>Membrane Proteins - metabolism</topic><topic>Middle Aged</topic><topic>Neutrophil collagenase</topic><topic>Periodontitis</topic><topic>Polymerase chain reaction</topic><topic>Protein expression</topic><topic>Protein kinase</topic><topic>Proteins</topic><topic>Real-Time Polymerase Chain Reaction</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Aung, W. P. P.</creatorcontrib><creatorcontrib>Chotjumlong, P.</creatorcontrib><creatorcontrib>Pata, S.</creatorcontrib><creatorcontrib>Montreekachon, P.</creatorcontrib><creatorcontrib>Supanchart, C.</creatorcontrib><creatorcontrib>Khongkhunthian, S.</creatorcontrib><creatorcontrib>Sastraruji, T.</creatorcontrib><creatorcontrib>Krisanaprakornkit, S.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of periodontal research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Aung, W. P. P.</au><au>Chotjumlong, P.</au><au>Pata, S.</au><au>Montreekachon, P.</au><au>Supanchart, C.</au><au>Khongkhunthian, S.</au><au>Sastraruji, T.</au><au>Krisanaprakornkit, S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inducible expression of A Disintegrin and Metalloproteinase 8 in chronic periodontitis and gingival epithelial cells</atitle><jtitle>Journal of periodontal research</jtitle><addtitle>J Periodontal Res</addtitle><date>2017-06</date><risdate>2017</risdate><volume>52</volume><issue>3</issue><spage>582</spage><epage>593</epage><pages>582-593</pages><issn>0022-3484</issn><eissn>1600-0765</eissn><abstract>Background and Objectives The expression of A Disintegrin and Metalloproteinase 8 (ADAM8) is associated with several inflammatory diseases. Elevated ADAM8 levels have been shown in gingival crevicular fluid of patients with chronic periodontitis. The objective of this study was to investigate ADAM8 expression in chronic periodontitis tissues compared with that in normal tissues. ADAM8 expression and its inductive mechanism were examined in human gingival epithelial cells (HGECs) and human gingival fibroblasts. Material and Methods Total RNA and protein were extracted from gingival biopsies of 33 patients with chronic periodontitis and those of 23 healthy volunteers. ADAM8 mRNA and protein expression was analyzed by real‐time polymerase chain reaction, immunoblotting and immunohistochemistry. ADAM8 expression in control and stimulated cells in the presence or absence of specific inhibitors for mitogen‐activated protein kinase pathways was assayed by real‐time polymerase chain reaction, immunoblotting, flow cytometry and immunofluorescence. Results ADAM8 mRNA and protein expression in chronic periodontitis tissues was significantly greater than that in normal tissues (p &lt; 0.01). Significantly increased ADAM8 expression was detected in the gingival epithelium of chronic periodontitis tissues (p &lt; 0.001). ADAM8 mRNA expression in HGECs, but not in human gingival fibroblasts, was significantly induced by stimulation with Fusobacterium nucleatum (p &lt; 0.05), partially via the p44/42 mitogen‐activated protein kinase pathway. ADAM8 expression in the cell lysates and on the surface of HGECs was induced by stimulation with F. nucleatum. Conclusion ADAM8 expression is increased in inflamed chronic periodontitis tissues and localized within gingival epithelium, consistent with an upregulation of ADAM8 expression in F. nucleatum‐stimulated HGECs, suggesting a possible role of ADAM8 in innate immunity of periodontal tissue.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>27859260</pmid><doi>10.1111/jre.12426</doi><tpages>12</tpages></addata></record>
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subjects A Disintegrin and Metalloproteinase 8
ADAM protein
ADAM Proteins - metabolism
ADAM8 protein
Adult
Blotting, Western
Case-Control Studies
chronic periodontitis
Chronic Periodontitis - metabolism
Dentistry
Epithelial cells
Epithelial Cells - metabolism
Epithelium
Fibroblasts
Flow Cytometry
Fluorescent Antibody Technique
Fusobacterium nucleatum
Gene expression
Gingiva
Gingiva - cytology
Gingiva - metabolism
Gum disease
Humans
Immunoblotting
Immunofluorescence
Immunohistochemistry
Inflammatory diseases
Innate immunity
Kinases
Lysates
MAP kinase
Matrix Metalloproteinase 8 - metabolism
Membrane Proteins - metabolism
Middle Aged
Neutrophil collagenase
Periodontitis
Polymerase chain reaction
Protein expression
Protein kinase
Proteins
Real-Time Polymerase Chain Reaction
Young Adult
title Inducible expression of A Disintegrin and Metalloproteinase 8 in chronic periodontitis and gingival epithelial cells
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