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High-mobility group box 1 expression in mandibular bone cells of experimental periodontitis
Background: High-mobility group box 1 (HMGB1) was suggested to be associated with the pathogenesis of chronic periodontitis which characterized by alveolar bone loss. HMGB1 was defined as a bone-active cytokine, but the rule of HMGB1 in bone loss of chronic periodontitis is still understood. Aim: Th...
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Published in: | Contemporary clinical dentistry 2019-07, Vol.10 (3), p.525-530 |
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description | Background: High-mobility group box 1 (HMGB1) was suggested to be associated with the pathogenesis of chronic periodontitis which characterized by alveolar bone loss. HMGB1 was defined as a bone-active cytokine, but the rule of HMGB1 in bone loss of chronic periodontitis is still understood. Aim: The aim of this study is to investigate the expression of HMGB1 on osteoblasts and osteoclasts in the mandible of chronic periodontitis. Methods: This experimental study was conducted to rats injected by Porphyromonas gingivalis into the buccal and lingual subgingival area at a concentration of 2 × 109 CFU/mL three times a week with 2-day apart for 2, 3, 4, and 6 weeks as chronic periodontitis group and injected by normal saline as control group. Analysis of variance was used to examine the differences between groups followed by least significant difference post hoc test with the level of significance was |
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HMGB1 was defined as a bone-active cytokine, but the rule of HMGB1 in bone loss of chronic periodontitis is still understood. Aim: The aim of this study is to investigate the expression of HMGB1 on osteoblasts and osteoclasts in the mandible of chronic periodontitis. Methods: This experimental study was conducted to rats injected by Porphyromonas gingivalis into the buccal and lingual subgingival area at a concentration of 2 × 109 CFU/mL three times a week with 2-day apart for 2, 3, 4, and 6 weeks as chronic periodontitis group and injected by normal saline as control group. Analysis of variance was used to examine the differences between groups followed by least significant difference post hoc test with the level of significance was <0.05. Results: The HMGB1 expression was found in both osteoclasts and osteoblasts of mandibular bone by immunohistochemistry analysis. There was a difference of HMGB1 expression on osteoblasts and osteoclasts of chronic periodontitis. HMGB1 expression was found increased significantly in mandibular osteoblasts of chronic periodontitis, whereas the HMGB1 expression in mandibular osteoclast is higher in 2 and 3 weeks, but it was lower in 4 and 6 weeks. Conclusions: This study indicated a potential role for HMGB1 in bone loss of chronic periodontitis. HMGB1 on mandibular osteoclasts and osteoblasts may play different rules in the onset and progression of chronic periodontitis.</description><identifier>ISSN: 0976-237X</identifier><identifier>EISSN: 0976-2361</identifier><identifier>DOI: 10.4103/ccd.ccd_907_18</identifier><identifier>PMID: 32308332</identifier><language>eng</language><publisher>India: Wolters Kluwer India Pvt. Ltd</publisher><subject>Alveolar bone ; Analysis ; Bone loss ; Bone marrow ; Chromosomal proteins ; chronic periodontitis ; Cytokines ; Cytoplasm ; EDTA ; Ethylenediaminetetraacetic acid ; Gum disease ; high-mobility group box 1 ; HMGB1 protein ; Immunohistochemistry ; Inflammation ; Mandible ; mandibular bone cell ; Mobility ; Original ; Osteoblasts ; osteoblasts/osteoclasts ; Osteoclasts ; Pathogenesis ; Periodontitis ; Tumor necrosis factor-TNF</subject><ispartof>Contemporary clinical dentistry, 2019-07, Vol.10 (3), p.525-530</ispartof><rights>Copyright: © 2020 Contemporary Clinical Dentistry.</rights><rights>COPYRIGHT 2019 Medknow Publications and Media Pvt. Ltd.</rights><rights>2019. This work is published under https://creativecommons.org/licenses/by-nc-sa/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2019. This article is published under (http://creativecommons.org/licenses/by-nc-sa/3.0/) (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Copyright: © 2020 Contemporary Clinical Dentistry 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c770y-64cce257b4e9a1b4bc007f400cf6b61586c4f7d1b15b3622a847b168194ae4bf3</citedby><cites>FETCH-LOGICAL-c770y-64cce257b4e9a1b4bc007f400cf6b61586c4f7d1b15b3622a847b168194ae4bf3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7150575/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2377626890?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32308332$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Da'at Arina, Yuliana</creatorcontrib><creatorcontrib>Rubianto, Mohamad</creatorcontrib><creatorcontrib>Ferdiansyah, F</creatorcontrib><creatorcontrib>Sudiana, I</creatorcontrib><creatorcontrib>Rahayu, Retno</creatorcontrib><creatorcontrib>Notobroto, Hari</creatorcontrib><title>High-mobility group box 1 expression in mandibular bone cells of experimental periodontitis</title><title>Contemporary clinical dentistry</title><addtitle>Contemp Clin Dent</addtitle><description>Background: High-mobility group box 1 (HMGB1) was suggested to be associated with the pathogenesis of chronic periodontitis which characterized by alveolar bone loss. HMGB1 was defined as a bone-active cytokine, but the rule of HMGB1 in bone loss of chronic periodontitis is still understood. Aim: The aim of this study is to investigate the expression of HMGB1 on osteoblasts and osteoclasts in the mandible of chronic periodontitis. Methods: This experimental study was conducted to rats injected by Porphyromonas gingivalis into the buccal and lingual subgingival area at a concentration of 2 × 109 CFU/mL three times a week with 2-day apart for 2, 3, 4, and 6 weeks as chronic periodontitis group and injected by normal saline as control group. Analysis of variance was used to examine the differences between groups followed by least significant difference post hoc test with the level of significance was <0.05. Results: The HMGB1 expression was found in both osteoclasts and osteoblasts of mandibular bone by immunohistochemistry analysis. There was a difference of HMGB1 expression on osteoblasts and osteoclasts of chronic periodontitis. HMGB1 expression was found increased significantly in mandibular osteoblasts of chronic periodontitis, whereas the HMGB1 expression in mandibular osteoclast is higher in 2 and 3 weeks, but it was lower in 4 and 6 weeks. Conclusions: This study indicated a potential role for HMGB1 in bone loss of chronic periodontitis. HMGB1 on mandibular osteoclasts and osteoblasts may play different rules in the onset and progression of chronic periodontitis.</description><subject>Alveolar bone</subject><subject>Analysis</subject><subject>Bone loss</subject><subject>Bone marrow</subject><subject>Chromosomal proteins</subject><subject>chronic periodontitis</subject><subject>Cytokines</subject><subject>Cytoplasm</subject><subject>EDTA</subject><subject>Ethylenediaminetetraacetic acid</subject><subject>Gum disease</subject><subject>high-mobility group box 1</subject><subject>HMGB1 protein</subject><subject>Immunohistochemistry</subject><subject>Inflammation</subject><subject>Mandible</subject><subject>mandibular bone cell</subject><subject>Mobility</subject><subject>Original</subject><subject>Osteoblasts</subject><subject>osteoblasts/osteoclasts</subject><subject>Osteoclasts</subject><subject>Pathogenesis</subject><subject>Periodontitis</subject><subject>Tumor necrosis factor-TNF</subject><issn>0976-237X</issn><issn>0976-2361</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqNk89r2zAUx83YWEvX647DMBi7JNNv2ZdBKd1aKOyywWAHIclSolS2Mslumv9-ctOmyejCbIyF9HlfPb2nb1G8hWBKIMCftG6m-RM14AJWL4pjUHM2QZjBl9sx_3lUnKa0APnBNQGUvC6OMMKgwhgdF78u3Ww-aYNy3vXrchbDsCxVuCthae6W0aTkQle6rmxl1zg1eBnzcmdKbbxPZbAjZqJrTddLX47D0ISud71Lb4pXVvpkTh_-J8WPLxffzy8n19--Xp2fXU8052A9YURrgyhXxNQSKqI0ANwSALRlikFaMU0sb6CCVGGGkKwIV5BVsCbSEGXxSXG10W2CXIhlTkbGtQjSifuJEGdCxt5pb4RGDDKkGoi4JKxpKmqVopZyyQDWHGStzxut5aBa0-h8rCj9nuj-SufmYhZuBYcUUE6zwMcHgRh-Dyb1onVpLJbsTBiSQLhGhNYMVhl9_xe6CEPscqkEhhBSDkh9kMrd5QyxqgZP1EzmY7rOhpydHrcWZ7lSEKG6ogcpBjmrEYIoU9NnqPw2pnU6N9-6PL8n-18Buzt82AmYG-n7eQp-6PNlS_vKB8FnctYxpBSN3bYMAjGaRYxGeTJLDni32-gt_miNDFxsgFXwvYnpxg8rE0Vmb7qw-oesoIiKPUvhP9_cJFg</recordid><startdate>20190701</startdate><enddate>20190701</enddate><creator>Da'at Arina, Yuliana</creator><creator>Rubianto, Mohamad</creator><creator>Ferdiansyah, F</creator><creator>Sudiana, I</creator><creator>Rahayu, Retno</creator><creator>Notobroto, Hari</creator><general>Wolters Kluwer India Pvt. 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Rubianto, Mohamad ; Ferdiansyah, F ; Sudiana, I ; Rahayu, Retno ; Notobroto, Hari</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c770y-64cce257b4e9a1b4bc007f400cf6b61586c4f7d1b15b3622a847b168194ae4bf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Alveolar bone</topic><topic>Analysis</topic><topic>Bone loss</topic><topic>Bone marrow</topic><topic>Chromosomal proteins</topic><topic>chronic periodontitis</topic><topic>Cytokines</topic><topic>Cytoplasm</topic><topic>EDTA</topic><topic>Ethylenediaminetetraacetic acid</topic><topic>Gum disease</topic><topic>high-mobility group box 1</topic><topic>HMGB1 protein</topic><topic>Immunohistochemistry</topic><topic>Inflammation</topic><topic>Mandible</topic><topic>mandibular bone cell</topic><topic>Mobility</topic><topic>Original</topic><topic>Osteoblasts</topic><topic>osteoblasts/osteoclasts</topic><topic>Osteoclasts</topic><topic>Pathogenesis</topic><topic>Periodontitis</topic><topic>Tumor necrosis factor-TNF</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Da'at Arina, Yuliana</creatorcontrib><creatorcontrib>Rubianto, Mohamad</creatorcontrib><creatorcontrib>Ferdiansyah, F</creatorcontrib><creatorcontrib>Sudiana, I</creatorcontrib><creatorcontrib>Rahayu, Retno</creatorcontrib><creatorcontrib>Notobroto, Hari</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Complete (ProQuest Database)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>ProQuest research library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>Contemporary clinical dentistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Da'at Arina, Yuliana</au><au>Rubianto, Mohamad</au><au>Ferdiansyah, F</au><au>Sudiana, I</au><au>Rahayu, Retno</au><au>Notobroto, Hari</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>High-mobility group box 1 expression in mandibular bone cells of experimental periodontitis</atitle><jtitle>Contemporary clinical dentistry</jtitle><addtitle>Contemp Clin Dent</addtitle><date>2019-07-01</date><risdate>2019</risdate><volume>10</volume><issue>3</issue><spage>525</spage><epage>530</epage><pages>525-530</pages><issn>0976-237X</issn><eissn>0976-2361</eissn><abstract>Background: High-mobility group box 1 (HMGB1) was suggested to be associated with the pathogenesis of chronic periodontitis which characterized by alveolar bone loss. HMGB1 was defined as a bone-active cytokine, but the rule of HMGB1 in bone loss of chronic periodontitis is still understood. Aim: The aim of this study is to investigate the expression of HMGB1 on osteoblasts and osteoclasts in the mandible of chronic periodontitis. Methods: This experimental study was conducted to rats injected by Porphyromonas gingivalis into the buccal and lingual subgingival area at a concentration of 2 × 109 CFU/mL three times a week with 2-day apart for 2, 3, 4, and 6 weeks as chronic periodontitis group and injected by normal saline as control group. Analysis of variance was used to examine the differences between groups followed by least significant difference post hoc test with the level of significance was <0.05. Results: The HMGB1 expression was found in both osteoclasts and osteoblasts of mandibular bone by immunohistochemistry analysis. There was a difference of HMGB1 expression on osteoblasts and osteoclasts of chronic periodontitis. HMGB1 expression was found increased significantly in mandibular osteoblasts of chronic periodontitis, whereas the HMGB1 expression in mandibular osteoclast is higher in 2 and 3 weeks, but it was lower in 4 and 6 weeks. Conclusions: This study indicated a potential role for HMGB1 in bone loss of chronic periodontitis. HMGB1 on mandibular osteoclasts and osteoblasts may play different rules in the onset and progression of chronic periodontitis.</abstract><cop>India</cop><pub>Wolters Kluwer India Pvt. Ltd</pub><pmid>32308332</pmid><doi>10.4103/ccd.ccd_907_18</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Alveolar bone Analysis Bone loss Bone marrow Chromosomal proteins chronic periodontitis Cytokines Cytoplasm EDTA Ethylenediaminetetraacetic acid Gum disease high-mobility group box 1 HMGB1 protein Immunohistochemistry Inflammation Mandible mandibular bone cell Mobility Original Osteoblasts osteoblasts/osteoclasts Osteoclasts Pathogenesis Periodontitis Tumor necrosis factor-TNF |
title | High-mobility group box 1 expression in mandibular bone cells of experimental periodontitis |
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