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Increased expression of angiopoietin‐like protein 4 regulates matrix metalloproteinase‐13 expression in Porphyromonas gingivalis lipopolysaccharides‐stimulated gingival fibroblasts and ligature‐induced experimental periodontitis
Background Angiopoietin‐like protein 4 (ANGPTL4) is produced in chronic or acute inflammation. Although ANGPTL4 increases in the periodontal ligament fibroblasts during hypoxia, the involvement and role of ANGPTL4 in periodontitis have not been elucidated. Objective In this study, we investigated wh...
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Published in: | Journal of periodontal research 2023-02, Vol.58 (1), p.43-52 |
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creator | Kondo, Shun Kojima, Kento Nakamura, Nobuhisa Miyabe, Megumi Kikuchi, Takeshi Ohno, Tasuku Sawada, Noritaka Minato, Tomomi Saiki, Tomokazu Ito, Mizuho Sasajima, Sachiko Matsubara, Tatsuaki Mitani, Akio Naruse, Keiko |
description | Background
Angiopoietin‐like protein 4 (ANGPTL4) is produced in chronic or acute inflammation. Although ANGPTL4 increases in the periodontal ligament fibroblasts during hypoxia, the involvement and role of ANGPTL4 in periodontitis have not been elucidated.
Objective
In this study, we investigated whether ligature‐induced experimental periodontitis and/or Porphyromonas gingivalis lipopolysaccharides (Pg‐LPS) would upregulate ANGPTL4 expression and whether ANGPTL4 would somehow involve in the expression of matrix metalloproteinases (MMPs) which are key molecules in the process of periodontal tissue destruction.
Methods
Experimental periodontitis was induced in 6‐week‐old male Sprague–Dawley rats by placing a nylon suture around the neck of the maxillary second molar. Two weeks after the induction of periodontitis, the periodontal tissue was excised and analyzed by histological/immunohistochemical staining and gene expression analyses. Human gingival fibroblasts (hGFs) were stimulated with Pg‐LPS. The gene expression of ANGPTLs and receptors involved in ANGPTL4 recognition were observed. We also confirmed the changes in gene expression of MMPs upon stimulation with human ANGPTL4. Furthermore, we downregulated ANGPTL4 expression by short interfering RNA in hGFs and investigated the effect of Pg‐LPS on MMP production.
Results
Induction of periodontitis significantly increased the expression of ANGPTL4 in the gingiva. Pg‐LPS significantly increased the gene and protein expression of ANGPTL4 in hGFs but not the gene expression of other ANGPTLs or ANGPTL receptors. Recombinant human ANGPTL4 significantly increased MMP13 gene expression in hGFs. We also confirmed that MMP13 expression was increased in the gingiva during experimental periodontitis. Pg‐LPS induced MMP13 gene expression in hGFs. These results suggest the pivotal role of ANGPTL4 in periodontitis.
Conclusion
Periodontitis increases ANGPTL4 expression in the gingiva, further suggesting that increased ANGPTL4 may be a factor involved in enhancing MMP13 expression. |
doi_str_mv | 10.1111/jre.13067 |
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Angiopoietin‐like protein 4 (ANGPTL4) is produced in chronic or acute inflammation. Although ANGPTL4 increases in the periodontal ligament fibroblasts during hypoxia, the involvement and role of ANGPTL4 in periodontitis have not been elucidated.
Objective
In this study, we investigated whether ligature‐induced experimental periodontitis and/or Porphyromonas gingivalis lipopolysaccharides (Pg‐LPS) would upregulate ANGPTL4 expression and whether ANGPTL4 would somehow involve in the expression of matrix metalloproteinases (MMPs) which are key molecules in the process of periodontal tissue destruction.
Methods
Experimental periodontitis was induced in 6‐week‐old male Sprague–Dawley rats by placing a nylon suture around the neck of the maxillary second molar. Two weeks after the induction of periodontitis, the periodontal tissue was excised and analyzed by histological/immunohistochemical staining and gene expression analyses. Human gingival fibroblasts (hGFs) were stimulated with Pg‐LPS. The gene expression of ANGPTLs and receptors involved in ANGPTL4 recognition were observed. We also confirmed the changes in gene expression of MMPs upon stimulation with human ANGPTL4. Furthermore, we downregulated ANGPTL4 expression by short interfering RNA in hGFs and investigated the effect of Pg‐LPS on MMP production.
Results
Induction of periodontitis significantly increased the expression of ANGPTL4 in the gingiva. Pg‐LPS significantly increased the gene and protein expression of ANGPTL4 in hGFs but not the gene expression of other ANGPTLs or ANGPTL receptors. Recombinant human ANGPTL4 significantly increased MMP13 gene expression in hGFs. We also confirmed that MMP13 expression was increased in the gingiva during experimental periodontitis. Pg‐LPS induced MMP13 gene expression in hGFs. These results suggest the pivotal role of ANGPTL4 in periodontitis.
Conclusion
Periodontitis increases ANGPTL4 expression in the gingiva, further suggesting that increased ANGPTL4 may be a factor involved in enhancing MMP13 expression.</description><identifier>ISSN: 0022-3484</identifier><identifier>EISSN: 1600-0765</identifier><identifier>DOI: 10.1111/jre.13067</identifier><identifier>PMID: 36409042</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Angiopoietin ; Angiopoietin-Like Protein 4 - metabolism ; ANGPTL4 ; Animals ; Cells, Cultured ; Collagenase 3 ; Fibroblasts ; Fibroblasts - metabolism ; Gene expression ; Gingiva ; Gingiva - metabolism ; gingival fibroblasts ; Gum disease ; Humans ; Hypoxia ; Lipopolysaccharides ; Lipopolysaccharides - pharmacology ; Male ; Matrix metalloproteinase ; Matrix Metalloproteinase 13 - metabolism ; Matrix Metalloproteinase 13 - pharmacology ; Metalloproteinase ; MMP ; Periodontal ligament ; Periodontitis ; Periodontitis - metabolism ; Porphyromonas gingivalis ; Proteins ; Rats ; Rats, Sprague-Dawley ; siRNA</subject><ispartof>Journal of periodontal research, 2023-02, Vol.58 (1), p.43-52</ispartof><rights>2022 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.</rights><rights>2023 John Wiley & Sons A/S</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3497-f23994819dcc4b88e9e1147394025334739da96324362a6dfbeffc97e3d5a48a3</citedby><cites>FETCH-LOGICAL-c3497-f23994819dcc4b88e9e1147394025334739da96324362a6dfbeffc97e3d5a48a3</cites><orcidid>0000-0002-0062-0694</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36409042$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kondo, Shun</creatorcontrib><creatorcontrib>Kojima, Kento</creatorcontrib><creatorcontrib>Nakamura, Nobuhisa</creatorcontrib><creatorcontrib>Miyabe, Megumi</creatorcontrib><creatorcontrib>Kikuchi, Takeshi</creatorcontrib><creatorcontrib>Ohno, Tasuku</creatorcontrib><creatorcontrib>Sawada, Noritaka</creatorcontrib><creatorcontrib>Minato, Tomomi</creatorcontrib><creatorcontrib>Saiki, Tomokazu</creatorcontrib><creatorcontrib>Ito, Mizuho</creatorcontrib><creatorcontrib>Sasajima, Sachiko</creatorcontrib><creatorcontrib>Matsubara, Tatsuaki</creatorcontrib><creatorcontrib>Mitani, Akio</creatorcontrib><creatorcontrib>Naruse, Keiko</creatorcontrib><title>Increased expression of angiopoietin‐like protein 4 regulates matrix metalloproteinase‐13 expression in Porphyromonas gingivalis lipopolysaccharides‐stimulated gingival fibroblasts and ligature‐induced experimental periodontitis</title><title>Journal of periodontal research</title><addtitle>J Periodontal Res</addtitle><description>Background
Angiopoietin‐like protein 4 (ANGPTL4) is produced in chronic or acute inflammation. Although ANGPTL4 increases in the periodontal ligament fibroblasts during hypoxia, the involvement and role of ANGPTL4 in periodontitis have not been elucidated.
Objective
In this study, we investigated whether ligature‐induced experimental periodontitis and/or Porphyromonas gingivalis lipopolysaccharides (Pg‐LPS) would upregulate ANGPTL4 expression and whether ANGPTL4 would somehow involve in the expression of matrix metalloproteinases (MMPs) which are key molecules in the process of periodontal tissue destruction.
Methods
Experimental periodontitis was induced in 6‐week‐old male Sprague–Dawley rats by placing a nylon suture around the neck of the maxillary second molar. Two weeks after the induction of periodontitis, the periodontal tissue was excised and analyzed by histological/immunohistochemical staining and gene expression analyses. Human gingival fibroblasts (hGFs) were stimulated with Pg‐LPS. The gene expression of ANGPTLs and receptors involved in ANGPTL4 recognition were observed. We also confirmed the changes in gene expression of MMPs upon stimulation with human ANGPTL4. Furthermore, we downregulated ANGPTL4 expression by short interfering RNA in hGFs and investigated the effect of Pg‐LPS on MMP production.
Results
Induction of periodontitis significantly increased the expression of ANGPTL4 in the gingiva. Pg‐LPS significantly increased the gene and protein expression of ANGPTL4 in hGFs but not the gene expression of other ANGPTLs or ANGPTL receptors. Recombinant human ANGPTL4 significantly increased MMP13 gene expression in hGFs. We also confirmed that MMP13 expression was increased in the gingiva during experimental periodontitis. Pg‐LPS induced MMP13 gene expression in hGFs. These results suggest the pivotal role of ANGPTL4 in periodontitis.
Conclusion
Periodontitis increases ANGPTL4 expression in the gingiva, further suggesting that increased ANGPTL4 may be a factor involved in enhancing MMP13 expression.</description><subject>Angiopoietin</subject><subject>Angiopoietin-Like Protein 4 - metabolism</subject><subject>ANGPTL4</subject><subject>Animals</subject><subject>Cells, Cultured</subject><subject>Collagenase 3</subject><subject>Fibroblasts</subject><subject>Fibroblasts - metabolism</subject><subject>Gene expression</subject><subject>Gingiva</subject><subject>Gingiva - metabolism</subject><subject>gingival fibroblasts</subject><subject>Gum disease</subject><subject>Humans</subject><subject>Hypoxia</subject><subject>Lipopolysaccharides</subject><subject>Lipopolysaccharides - pharmacology</subject><subject>Male</subject><subject>Matrix metalloproteinase</subject><subject>Matrix Metalloproteinase 13 - metabolism</subject><subject>Matrix Metalloproteinase 13 - pharmacology</subject><subject>Metalloproteinase</subject><subject>MMP</subject><subject>Periodontal ligament</subject><subject>Periodontitis</subject><subject>Periodontitis - metabolism</subject><subject>Porphyromonas gingivalis</subject><subject>Proteins</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>siRNA</subject><issn>0022-3484</issn><issn>1600-0765</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp1ks1u1DAUhS0EokNhwQsgS2xgkdaOPflZoqpAUSUQgnXk2DdTD44dbKd0djwCz8iah-BOM1QICW9sS9855177EvKUsxOO63Qb4YQLVtX3yIpXjBWsrtb3yYqxsiyEbOQReZTSluG9qtuH5EhUkrVMlivy68LrCCqBoXAzRUjJBk_DQJXf2DAFC9n6n99_OPsF6BRDBuuppBE2s1MZEh1VjvaGjpCVc-FAoB9quPjbE3UfQpyudjGMAQm6sRhxrZxN1NkJs9wuKa2vVLQGEupTtuNtirlj6WD7GHqnUk5YokHlRuU57uOsN7Ne-oBoR_BYEd0fgwk-22zTY_JgUC7Bk8N-TD6_Pv909ra4fP_m4uzVZaGFbOtiKEXbyoa3RmvZNw20wLmsRStZuRZifzKqrUQpRVWqygw9DINuaxBmrWSjxDF5sfjic3ydIeVutEmDc8pDmFNX1qKR6CYEos__Qbdhjh6rQ6pa1w1GcqReLpSOIaUIQzdhhyruOs66_Qh0OALd7Qgg--zgOPcjmDvyz58jcLoA36yD3f-duncfzxfL3_6rx1I</recordid><startdate>202302</startdate><enddate>202302</enddate><creator>Kondo, Shun</creator><creator>Kojima, Kento</creator><creator>Nakamura, Nobuhisa</creator><creator>Miyabe, Megumi</creator><creator>Kikuchi, Takeshi</creator><creator>Ohno, Tasuku</creator><creator>Sawada, Noritaka</creator><creator>Minato, Tomomi</creator><creator>Saiki, Tomokazu</creator><creator>Ito, Mizuho</creator><creator>Sasajima, Sachiko</creator><creator>Matsubara, Tatsuaki</creator><creator>Mitani, Akio</creator><creator>Naruse, Keiko</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><orcidid>https://orcid.org/0000-0002-0062-0694</orcidid></search><sort><creationdate>202302</creationdate><title>Increased expression of angiopoietin‐like protein 4 regulates matrix metalloproteinase‐13 expression in Porphyromonas gingivalis lipopolysaccharides‐stimulated gingival fibroblasts and ligature‐induced experimental periodontitis</title><author>Kondo, Shun ; Kojima, Kento ; Nakamura, Nobuhisa ; Miyabe, Megumi ; Kikuchi, Takeshi ; Ohno, Tasuku ; Sawada, Noritaka ; Minato, Tomomi ; Saiki, Tomokazu ; Ito, Mizuho ; Sasajima, Sachiko ; Matsubara, Tatsuaki ; Mitani, Akio ; Naruse, Keiko</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3497-f23994819dcc4b88e9e1147394025334739da96324362a6dfbeffc97e3d5a48a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Angiopoietin</topic><topic>Angiopoietin-Like Protein 4 - metabolism</topic><topic>ANGPTL4</topic><topic>Animals</topic><topic>Cells, Cultured</topic><topic>Collagenase 3</topic><topic>Fibroblasts</topic><topic>Fibroblasts - metabolism</topic><topic>Gene expression</topic><topic>Gingiva</topic><topic>Gingiva - metabolism</topic><topic>gingival fibroblasts</topic><topic>Gum disease</topic><topic>Humans</topic><topic>Hypoxia</topic><topic>Lipopolysaccharides</topic><topic>Lipopolysaccharides - pharmacology</topic><topic>Male</topic><topic>Matrix metalloproteinase</topic><topic>Matrix Metalloproteinase 13 - metabolism</topic><topic>Matrix Metalloproteinase 13 - pharmacology</topic><topic>Metalloproteinase</topic><topic>MMP</topic><topic>Periodontal ligament</topic><topic>Periodontitis</topic><topic>Periodontitis - metabolism</topic><topic>Porphyromonas gingivalis</topic><topic>Proteins</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>siRNA</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kondo, Shun</creatorcontrib><creatorcontrib>Kojima, Kento</creatorcontrib><creatorcontrib>Nakamura, Nobuhisa</creatorcontrib><creatorcontrib>Miyabe, Megumi</creatorcontrib><creatorcontrib>Kikuchi, Takeshi</creatorcontrib><creatorcontrib>Ohno, Tasuku</creatorcontrib><creatorcontrib>Sawada, Noritaka</creatorcontrib><creatorcontrib>Minato, Tomomi</creatorcontrib><creatorcontrib>Saiki, Tomokazu</creatorcontrib><creatorcontrib>Ito, Mizuho</creatorcontrib><creatorcontrib>Sasajima, Sachiko</creatorcontrib><creatorcontrib>Matsubara, Tatsuaki</creatorcontrib><creatorcontrib>Mitani, Akio</creatorcontrib><creatorcontrib>Naruse, Keiko</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 & Calcified Tissue Abstracts</collection><collection>ProQuest Health & 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>Kondo, Shun</au><au>Kojima, Kento</au><au>Nakamura, Nobuhisa</au><au>Miyabe, Megumi</au><au>Kikuchi, Takeshi</au><au>Ohno, Tasuku</au><au>Sawada, Noritaka</au><au>Minato, Tomomi</au><au>Saiki, Tomokazu</au><au>Ito, Mizuho</au><au>Sasajima, Sachiko</au><au>Matsubara, Tatsuaki</au><au>Mitani, Akio</au><au>Naruse, Keiko</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Increased expression of angiopoietin‐like protein 4 regulates matrix metalloproteinase‐13 expression in Porphyromonas gingivalis lipopolysaccharides‐stimulated gingival fibroblasts and ligature‐induced experimental periodontitis</atitle><jtitle>Journal of periodontal research</jtitle><addtitle>J Periodontal Res</addtitle><date>2023-02</date><risdate>2023</risdate><volume>58</volume><issue>1</issue><spage>43</spage><epage>52</epage><pages>43-52</pages><issn>0022-3484</issn><eissn>1600-0765</eissn><abstract>Background
Angiopoietin‐like protein 4 (ANGPTL4) is produced in chronic or acute inflammation. Although ANGPTL4 increases in the periodontal ligament fibroblasts during hypoxia, the involvement and role of ANGPTL4 in periodontitis have not been elucidated.
Objective
In this study, we investigated whether ligature‐induced experimental periodontitis and/or Porphyromonas gingivalis lipopolysaccharides (Pg‐LPS) would upregulate ANGPTL4 expression and whether ANGPTL4 would somehow involve in the expression of matrix metalloproteinases (MMPs) which are key molecules in the process of periodontal tissue destruction.
Methods
Experimental periodontitis was induced in 6‐week‐old male Sprague–Dawley rats by placing a nylon suture around the neck of the maxillary second molar. Two weeks after the induction of periodontitis, the periodontal tissue was excised and analyzed by histological/immunohistochemical staining and gene expression analyses. Human gingival fibroblasts (hGFs) were stimulated with Pg‐LPS. The gene expression of ANGPTLs and receptors involved in ANGPTL4 recognition were observed. We also confirmed the changes in gene expression of MMPs upon stimulation with human ANGPTL4. Furthermore, we downregulated ANGPTL4 expression by short interfering RNA in hGFs and investigated the effect of Pg‐LPS on MMP production.
Results
Induction of periodontitis significantly increased the expression of ANGPTL4 in the gingiva. Pg‐LPS significantly increased the gene and protein expression of ANGPTL4 in hGFs but not the gene expression of other ANGPTLs or ANGPTL receptors. Recombinant human ANGPTL4 significantly increased MMP13 gene expression in hGFs. We also confirmed that MMP13 expression was increased in the gingiva during experimental periodontitis. Pg‐LPS induced MMP13 gene expression in hGFs. These results suggest the pivotal role of ANGPTL4 in periodontitis.
Conclusion
Periodontitis increases ANGPTL4 expression in the gingiva, further suggesting that increased ANGPTL4 may be a factor involved in enhancing MMP13 expression.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>36409042</pmid><doi>10.1111/jre.13067</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-0062-0694</orcidid></addata></record> |
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subjects | Angiopoietin Angiopoietin-Like Protein 4 - metabolism ANGPTL4 Animals Cells, Cultured Collagenase 3 Fibroblasts Fibroblasts - metabolism Gene expression Gingiva Gingiva - metabolism gingival fibroblasts Gum disease Humans Hypoxia Lipopolysaccharides Lipopolysaccharides - pharmacology Male Matrix metalloproteinase Matrix Metalloproteinase 13 - metabolism Matrix Metalloproteinase 13 - pharmacology Metalloproteinase MMP Periodontal ligament Periodontitis Periodontitis - metabolism Porphyromonas gingivalis Proteins Rats Rats, Sprague-Dawley siRNA |
title | Increased expression of angiopoietin‐like protein 4 regulates matrix metalloproteinase‐13 expression in Porphyromonas gingivalis lipopolysaccharides‐stimulated gingival fibroblasts and ligature‐induced experimental periodontitis |
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