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Periodontal regeneration following transplantation of proliferating tissue derived from periodontal ligament into class III furcation defects in dogs
The aim of this study was to evaluate the healing of class III furcation defects following transplantation of proliferating tissue derived from periodontal ligament (pPDL). Two weeks after removing alveolar bone, pPDL was excised. Class III furcation defects were created in the mandibular premolars....
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Published in: | Biomedical Research 2006, Vol.27(3), pp.139-147 |
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creator | MURANO, Yoshinori OTA, Mikio KATAYAMA, Akihiko SUGITO, Hiroki SHIBUKAWA, Yoshihiro YAMADA, Satoru |
description | The aim of this study was to evaluate the healing of class III furcation defects following transplantation of proliferating tissue derived from periodontal ligament (pPDL). Two weeks after removing alveolar bone, pPDL was excised. Class III furcation defects were created in the mandibular premolars. pPDL was transplanted into the furcation defects in the experimental group, while no treatment was performed on the furcation defects in the controls. Two, four and eight weeks after surgery, histologic examination, quantitative RT-PCR, and immunohistochemistry were carried out. bFGF and VEGF mRNA showed a significant increase in pPDL. In the pPDL treatment group, new cementum regenerated around almost the entire circumference of the furcation, with new bone filling most of the defect, while the control group presented epithelial downgrowth and defects filled with connective tissue. These results provide histological evidence that pPDL plays an important role in wound healing by promoting periodontal regeneration in class III furcation defects. |
doi_str_mv | 10.2220/biomedres.27.139 |
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Two weeks after removing alveolar bone, pPDL was excised. Class III furcation defects were created in the mandibular premolars. pPDL was transplanted into the furcation defects in the experimental group, while no treatment was performed on the furcation defects in the controls. Two, four and eight weeks after surgery, histologic examination, quantitative RT-PCR, and immunohistochemistry were carried out. bFGF and VEGF mRNA showed a significant increase in pPDL. In the pPDL treatment group, new cementum regenerated around almost the entire circumference of the furcation, with new bone filling most of the defect, while the control group presented epithelial downgrowth and defects filled with connective tissue. These results provide histological evidence that pPDL plays an important role in wound healing by promoting periodontal regeneration in class III furcation defects.</description><identifier>ISSN: 0388-6107</identifier><identifier>EISSN: 1880-313X</identifier><identifier>DOI: 10.2220/biomedres.27.139</identifier><identifier>PMID: 16847360</identifier><language>eng</language><publisher>Japan: Biomedical Research Press</publisher><subject>Animals ; Bone and Bones - pathology ; Cell Proliferation ; Dental Cementum - pathology ; Dogs ; Fibroblast Growth Factor 2 - metabolism ; Furcation Defects - diagnosis ; Furcation Defects - etiology ; Periodontal Ligament - pathology ; Proliferating Cell Nuclear Antigen - metabolism ; Regeneration ; RNA, Messenger - metabolism ; Time Factors ; Tissue Transplantation - adverse effects ; Tissue Transplantation - methods ; Vascular Endothelial Growth Factor A - metabolism ; Wound Healing</subject><ispartof>Biomedical Research, 2006, Vol.27(3), pp.139-147</ispartof><rights>2006 Biomedical Research Press</rights><rights>Copyright Japan Science and Technology Agency 2006</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c594t-393840186d791cbfa4008cfd05ae1fd6b0a44a02a987c9bebec7575910d72dc73</citedby><cites>FETCH-LOGICAL-c594t-393840186d791cbfa4008cfd05ae1fd6b0a44a02a987c9bebec7575910d72dc73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1875,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16847360$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>MURANO, Yoshinori</creatorcontrib><creatorcontrib>OTA, Mikio</creatorcontrib><creatorcontrib>KATAYAMA, Akihiko</creatorcontrib><creatorcontrib>SUGITO, Hiroki</creatorcontrib><creatorcontrib>SHIBUKAWA, Yoshihiro</creatorcontrib><creatorcontrib>YAMADA, Satoru</creatorcontrib><title>Periodontal regeneration following transplantation of proliferating tissue derived from periodontal ligament into class III furcation defects in dogs</title><title>Biomedical Research</title><addtitle>Biomed. Res.</addtitle><description>The aim of this study was to evaluate the healing of class III furcation defects following transplantation of proliferating tissue derived from periodontal ligament (pPDL). Two weeks after removing alveolar bone, pPDL was excised. Class III furcation defects were created in the mandibular premolars. pPDL was transplanted into the furcation defects in the experimental group, while no treatment was performed on the furcation defects in the controls. Two, four and eight weeks after surgery, histologic examination, quantitative RT-PCR, and immunohistochemistry were carried out. bFGF and VEGF mRNA showed a significant increase in pPDL. In the pPDL treatment group, new cementum regenerated around almost the entire circumference of the furcation, with new bone filling most of the defect, while the control group presented epithelial downgrowth and defects filled with connective tissue. These results provide histological evidence that pPDL plays an important role in wound healing by promoting periodontal regeneration in class III furcation defects.</description><subject>Animals</subject><subject>Bone and Bones - pathology</subject><subject>Cell Proliferation</subject><subject>Dental Cementum - pathology</subject><subject>Dogs</subject><subject>Fibroblast Growth Factor 2 - metabolism</subject><subject>Furcation Defects - diagnosis</subject><subject>Furcation Defects - etiology</subject><subject>Periodontal Ligament - pathology</subject><subject>Proliferating Cell Nuclear Antigen - metabolism</subject><subject>Regeneration</subject><subject>RNA, Messenger - metabolism</subject><subject>Time Factors</subject><subject>Tissue Transplantation - adverse effects</subject><subject>Tissue Transplantation - methods</subject><subject>Vascular Endothelial Growth Factor A - metabolism</subject><subject>Wound Healing</subject><issn>0388-6107</issn><issn>1880-313X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNqFkUFrFDEYhoModlu9e5KA4G22yWRmkjlKqbpQsAcFbyGTfBmzZCZrkqn4Q_y_pp1lq168JITv-R7y8iL0ipJtXdfkcnBhAhMhbWu-pax_gjZUCFIxyr4-RRvChKg6SvgZOk9pT8qbCvYcndFONJx1ZIN-3UJ0wYQ5K48jjDBDVNmFGdvgffjh5hHnqOZ08KowD5Ng8SEG7-wDeg-4lBbApqjuwGAbw4QPf3i9G9UEc8ZuzgFrr1LCu90O2yXqVWnAgs6pANiEMb1Az6zyCV4e7wv05f3156uP1c2nD7urdzeVbvsmV6xnoiFUdIb3VA9WNYQIbQ1pFVBruoGoplGkVr3guh9gAM1b3vaUGF4bzdkFert6S57vC6QsJ5c0-JIVwpJkJ7qG077_L0jLT0RN2wK--QfchyXOJYSkTcd5R5uWFIqslI4hpQhWHqKbVPwpKZH3zcpTs7LmsjRbVl4fxctQJo8LxyoLcL0C-5TVCCdAxey0h7-NbD2K-DTX31SUMLPfWN--7Q</recordid><startdate>20060601</startdate><enddate>20060601</enddate><creator>MURANO, Yoshinori</creator><creator>OTA, Mikio</creator><creator>KATAYAMA, Akihiko</creator><creator>SUGITO, Hiroki</creator><creator>SHIBUKAWA, Yoshihiro</creator><creator>YAMADA, Satoru</creator><general>Biomedical Research Press</general><general>Japan Science and Technology Agency</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>7QO</scope><scope>7QP</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20060601</creationdate><title>Periodontal regeneration following transplantation of proliferating tissue derived from periodontal ligament into class III furcation defects in dogs</title><author>MURANO, Yoshinori ; OTA, Mikio ; KATAYAMA, Akihiko ; SUGITO, Hiroki ; SHIBUKAWA, Yoshihiro ; YAMADA, Satoru</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c594t-393840186d791cbfa4008cfd05ae1fd6b0a44a02a987c9bebec7575910d72dc73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Animals</topic><topic>Bone and Bones - pathology</topic><topic>Cell Proliferation</topic><topic>Dental Cementum - pathology</topic><topic>Dogs</topic><topic>Fibroblast Growth Factor 2 - metabolism</topic><topic>Furcation Defects - diagnosis</topic><topic>Furcation Defects - etiology</topic><topic>Periodontal Ligament - pathology</topic><topic>Proliferating Cell Nuclear Antigen - metabolism</topic><topic>Regeneration</topic><topic>RNA, Messenger - metabolism</topic><topic>Time Factors</topic><topic>Tissue Transplantation - adverse effects</topic><topic>Tissue Transplantation - methods</topic><topic>Vascular Endothelial Growth Factor A - metabolism</topic><topic>Wound Healing</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>MURANO, Yoshinori</creatorcontrib><creatorcontrib>OTA, Mikio</creatorcontrib><creatorcontrib>KATAYAMA, Akihiko</creatorcontrib><creatorcontrib>SUGITO, Hiroki</creatorcontrib><creatorcontrib>SHIBUKAWA, Yoshihiro</creatorcontrib><creatorcontrib>YAMADA, Satoru</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Biomedical Research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>MURANO, Yoshinori</au><au>OTA, Mikio</au><au>KATAYAMA, Akihiko</au><au>SUGITO, Hiroki</au><au>SHIBUKAWA, Yoshihiro</au><au>YAMADA, Satoru</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Periodontal regeneration following transplantation of proliferating tissue derived from periodontal ligament into class III furcation defects in dogs</atitle><jtitle>Biomedical Research</jtitle><addtitle>Biomed. Res.</addtitle><date>2006-06-01</date><risdate>2006</risdate><volume>27</volume><issue>3</issue><spage>139</spage><epage>147</epage><pages>139-147</pages><issn>0388-6107</issn><eissn>1880-313X</eissn><abstract>The aim of this study was to evaluate the healing of class III furcation defects following transplantation of proliferating tissue derived from periodontal ligament (pPDL). Two weeks after removing alveolar bone, pPDL was excised. Class III furcation defects were created in the mandibular premolars. pPDL was transplanted into the furcation defects in the experimental group, while no treatment was performed on the furcation defects in the controls. Two, four and eight weeks after surgery, histologic examination, quantitative RT-PCR, and immunohistochemistry were carried out. bFGF and VEGF mRNA showed a significant increase in pPDL. In the pPDL treatment group, new cementum regenerated around almost the entire circumference of the furcation, with new bone filling most of the defect, while the control group presented epithelial downgrowth and defects filled with connective tissue. These results provide histological evidence that pPDL plays an important role in wound healing by promoting periodontal regeneration in class III furcation defects.</abstract><cop>Japan</cop><pub>Biomedical Research Press</pub><pmid>16847360</pmid><doi>10.2220/biomedres.27.139</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Bone and Bones - pathology Cell Proliferation Dental Cementum - pathology Dogs Fibroblast Growth Factor 2 - metabolism Furcation Defects - diagnosis Furcation Defects - etiology Periodontal Ligament - pathology Proliferating Cell Nuclear Antigen - metabolism Regeneration RNA, Messenger - metabolism Time Factors Tissue Transplantation - adverse effects Tissue Transplantation - methods Vascular Endothelial Growth Factor A - metabolism Wound Healing |
title | Periodontal regeneration following transplantation of proliferating tissue derived from periodontal ligament into class III furcation defects in dogs |
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