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Dental follicle cells and treated dentin matrix scaffold for tissue engineering the tooth root
Abstract Tissue engineering strategies to reconstruct tooth roots are an effective therapy for the treatment of tooth loss. However, strategies to successfully regenerate tooth roots have not been developed and optimized. In the present study, rat dental follicle stem cells (DFCs) were characterized...
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Published in: | Biomaterials 2012-02, Vol.33 (5), p.1291-1302 |
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description | Abstract Tissue engineering strategies to reconstruct tooth roots are an effective therapy for the treatment of tooth loss. However, strategies to successfully regenerate tooth roots have not been developed and optimized. In the present study, rat dental follicle stem cells (DFCs) were characterized, followed by a thorough investigation of tooth roots regeneration for a combination of DFCs seeding cells, treated dentin matrix (TDM) scaffolds, and an inductive alveolar fossa microenvironment. Eighteen clones derived from single DFCs were harvested; however, only three clones were amplified successfully more than five passages and 90–95 days in culture. Following 270 days or 30 passages, the heterogeneous DFCs showed suitable characteristics for seeding cells to regenerate tooth roots. However, various features, such as variable proliferation rates, differentiation characteristics, apoptosis rates, and total lifespan were observed in DFCs and the three clones. Importantly, upon transplantation of DFCs combined with TDM for four weeks, root-like tissues stained positive for markers of dental pulp and periodontal tissues were regenerated in the alveolar fossa, but not in the skull and omental pockets. These results indicate that tooth roots were successfully regenerated and suggest that the combination of DFCs with TDM in the alveolar fossa is a feasible strategy for tooth roots regeneration. This strategy could be a promising approach for the treatment of clinical tooth loss and provides a perspective with potential applications to regeneration of other tissues and organs. |
doi_str_mv | 10.1016/j.biomaterials.2011.09.068 |
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However, strategies to successfully regenerate tooth roots have not been developed and optimized. In the present study, rat dental follicle stem cells (DFCs) were characterized, followed by a thorough investigation of tooth roots regeneration for a combination of DFCs seeding cells, treated dentin matrix (TDM) scaffolds, and an inductive alveolar fossa microenvironment. Eighteen clones derived from single DFCs were harvested; however, only three clones were amplified successfully more than five passages and 90–95 days in culture. Following 270 days or 30 passages, the heterogeneous DFCs showed suitable characteristics for seeding cells to regenerate tooth roots. However, various features, such as variable proliferation rates, differentiation characteristics, apoptosis rates, and total lifespan were observed in DFCs and the three clones. Importantly, upon transplantation of DFCs combined with TDM for four weeks, root-like tissues stained positive for markers of dental pulp and periodontal tissues were regenerated in the alveolar fossa, but not in the skull and omental pockets. These results indicate that tooth roots were successfully regenerated and suggest that the combination of DFCs with TDM in the alveolar fossa is a feasible strategy for tooth roots regeneration. This strategy could be a promising approach for the treatment of clinical tooth loss and provides a perspective with potential applications to regeneration of other tissues and organs.</description><identifier>ISSN: 0142-9612</identifier><identifier>EISSN: 1878-5905</identifier><identifier>DOI: 10.1016/j.biomaterials.2011.09.068</identifier><identifier>PMID: 22088889</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Advanced Basic Science ; Alkaline Phosphatase - metabolism ; Animals ; Apoptosis ; Cell Differentiation ; Cell Membrane - metabolism ; Cell Proliferation ; Clone Cells ; Colony-Forming Units Assay ; Dental follicle cells ; Dental Sac - cytology ; Dental Sac - enzymology ; Dentin - metabolism ; Dentistry ; Gene Expression Regulation ; Rats ; Rats, Sprague-Dawley ; Regeneration ; Scaffold ; Tissue Engineering - methods ; Tissue Scaffolds - chemistry ; Tooth ; Tooth root ; Tooth Root - pathology</subject><ispartof>Biomaterials, 2012-02, Vol.33 (5), p.1291-1302</ispartof><rights>2011</rights><rights>Crown Copyright © 2011. Published by Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c532t-748c2f3cb8aae31c8c4bd96ee23b58af69078e4b26b8af058bdd170659853cb93</citedby><cites>FETCH-LOGICAL-c532t-748c2f3cb8aae31c8c4bd96ee23b58af69078e4b26b8af058bdd170659853cb93</cites></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/22088889$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Guo, Weihua</creatorcontrib><creatorcontrib>Gong, Kun</creatorcontrib><creatorcontrib>Shi, Haigang</creatorcontrib><creatorcontrib>Zhu, Guoxiong</creatorcontrib><creatorcontrib>He, Yong</creatorcontrib><creatorcontrib>Ding, Bofu</creatorcontrib><creatorcontrib>Wen, Lingying</creatorcontrib><creatorcontrib>Jin, Yan</creatorcontrib><title>Dental follicle cells and treated dentin matrix scaffold for tissue engineering the tooth root</title><title>Biomaterials</title><addtitle>Biomaterials</addtitle><description>Abstract Tissue engineering strategies to reconstruct tooth roots are an effective therapy for the treatment of tooth loss. However, strategies to successfully regenerate tooth roots have not been developed and optimized. In the present study, rat dental follicle stem cells (DFCs) were characterized, followed by a thorough investigation of tooth roots regeneration for a combination of DFCs seeding cells, treated dentin matrix (TDM) scaffolds, and an inductive alveolar fossa microenvironment. Eighteen clones derived from single DFCs were harvested; however, only three clones were amplified successfully more than five passages and 90–95 days in culture. Following 270 days or 30 passages, the heterogeneous DFCs showed suitable characteristics for seeding cells to regenerate tooth roots. However, various features, such as variable proliferation rates, differentiation characteristics, apoptosis rates, and total lifespan were observed in DFCs and the three clones. Importantly, upon transplantation of DFCs combined with TDM for four weeks, root-like tissues stained positive for markers of dental pulp and periodontal tissues were regenerated in the alveolar fossa, but not in the skull and omental pockets. These results indicate that tooth roots were successfully regenerated and suggest that the combination of DFCs with TDM in the alveolar fossa is a feasible strategy for tooth roots regeneration. This strategy could be a promising approach for the treatment of clinical tooth loss and provides a perspective with potential applications to regeneration of other tissues and organs.</description><subject>Advanced Basic Science</subject><subject>Alkaline Phosphatase - metabolism</subject><subject>Animals</subject><subject>Apoptosis</subject><subject>Cell Differentiation</subject><subject>Cell Membrane - metabolism</subject><subject>Cell Proliferation</subject><subject>Clone Cells</subject><subject>Colony-Forming Units Assay</subject><subject>Dental follicle cells</subject><subject>Dental Sac - cytology</subject><subject>Dental Sac - enzymology</subject><subject>Dentin - metabolism</subject><subject>Dentistry</subject><subject>Gene Expression Regulation</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Regeneration</subject><subject>Scaffold</subject><subject>Tissue Engineering - methods</subject><subject>Tissue Scaffolds - chemistry</subject><subject>Tooth</subject><subject>Tooth root</subject><subject>Tooth Root - pathology</subject><issn>0142-9612</issn><issn>1878-5905</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNqNkk1vFSEUhonR2Gv1LxjixtWMfAwz4MLEtH4lTVyoWwkDZ1quXKjANPbfy-RWY1yVBYTkec97OC8IvaCkp4SOr_b97NPBVMjehNIzQmlPVE9G-QDtqJxkJxQRD9GO0IF1aqTsBD0pZU_anQzsMTphjMi21A59P4dYTcBLCsHbANhCCAWb6HDN0Dwcdo3wETfD7H_hYs3SYNcUGVdfygoY4qWP0NqJl7heAa4p1Suc2_4UPVpaj_Ds7jxF396_-3r2sbv4_OHT2duLzgrOajcN0rKF21kaA5xaaYfZqRGA8VlIs4yKTBKGmY2NWIiQs3N0IqNQUjSV4qfo5bHudU4_VyhVH3zZnmIipLVoRcUgBeH8HiRVnE5sauTrI2lzKiXDoq-zP5h8qynRWxB6r_8NQm9BaKJ0C6KJn9_ZrPMB3F_pn8k34PwIQBvLjYesi_UQLTifwVbtkr-fz5v_ytjgo7cm_IBbKPu05rhpqC5ME_1l-xLbj6CtMB2Gkf8Gv6y2yQ</recordid><startdate>20120201</startdate><enddate>20120201</enddate><creator>Guo, Weihua</creator><creator>Gong, Kun</creator><creator>Shi, Haigang</creator><creator>Zhu, Guoxiong</creator><creator>He, Yong</creator><creator>Ding, Bofu</creator><creator>Wen, Lingying</creator><creator>Jin, Yan</creator><general>Elsevier Ltd</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>7X8</scope><scope>7QO</scope><scope>7QP</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>20120201</creationdate><title>Dental follicle cells and treated dentin matrix scaffold for tissue engineering the tooth root</title><author>Guo, Weihua ; 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However, strategies to successfully regenerate tooth roots have not been developed and optimized. In the present study, rat dental follicle stem cells (DFCs) were characterized, followed by a thorough investigation of tooth roots regeneration for a combination of DFCs seeding cells, treated dentin matrix (TDM) scaffolds, and an inductive alveolar fossa microenvironment. Eighteen clones derived from single DFCs were harvested; however, only three clones were amplified successfully more than five passages and 90–95 days in culture. Following 270 days or 30 passages, the heterogeneous DFCs showed suitable characteristics for seeding cells to regenerate tooth roots. However, various features, such as variable proliferation rates, differentiation characteristics, apoptosis rates, and total lifespan were observed in DFCs and the three clones. Importantly, upon transplantation of DFCs combined with TDM for four weeks, root-like tissues stained positive for markers of dental pulp and periodontal tissues were regenerated in the alveolar fossa, but not in the skull and omental pockets. These results indicate that tooth roots were successfully regenerated and suggest that the combination of DFCs with TDM in the alveolar fossa is a feasible strategy for tooth roots regeneration. This strategy could be a promising approach for the treatment of clinical tooth loss and provides a perspective with potential applications to regeneration of other tissues and organs.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>22088889</pmid><doi>10.1016/j.biomaterials.2011.09.068</doi><tpages>12</tpages></addata></record> |
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subjects | Advanced Basic Science Alkaline Phosphatase - metabolism Animals Apoptosis Cell Differentiation Cell Membrane - metabolism Cell Proliferation Clone Cells Colony-Forming Units Assay Dental follicle cells Dental Sac - cytology Dental Sac - enzymology Dentin - metabolism Dentistry Gene Expression Regulation Rats Rats, Sprague-Dawley Regeneration Scaffold Tissue Engineering - methods Tissue Scaffolds - chemistry Tooth Tooth root Tooth Root - pathology |
title | Dental follicle cells and treated dentin matrix scaffold for tissue engineering the tooth root |
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