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Immunohistochemical Characterization of Rapid Dentin Formation Induced by Enamel Matrix Derivative

dc.contributor.authorNakamura, Y.en_US
dc.contributor.authorRitchie, Helena H.en_US
dc.contributor.authorMatsumoto, K.en_US
dc.contributor.authorLyngstadaas, S. P.en_US
dc.contributor.authorSlaby, I.en_US
dc.date.accessioned2006-09-11T19:39:25Z
dc.date.available2006-09-11T19:39:25Z
dc.date.issued2004-09en_US
dc.identifier.citationNakamura, Y.; Slaby, I.; Matsumoto, K.; Ritchie, H. H.; Lyngstadaas, S. P.; (2004). "Immunohistochemical Characterization of Rapid Dentin Formation Induced by Enamel Matrix Derivative." Calcified Tissue International 75(3): 243-252. <http://hdl.handle.net/2027.42/48011>en_US
dc.identifier.issn0171-967Xen_US
dc.identifier.issn1432-0827en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/48011
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=12566040&dopt=citationen_US
dc.description.abstractThe purpose of this study was to examine the pulpal expression of dentin-related proteins during enamel matrix derivative (EMD)–induced reparative dentin formation in a pulpotomy model in pig incisors. Pulpotomies were performed on 72 lower incisors in 24 adult miniature swine. The exposed pulp tissue was treated with EMD or covered with a calcium hydroxide paste (Dycal ® ). At predefined time-points, ranging from 4 days to 12 weeks, experimental teeth were extracted and examined by use of light microscopy, and expression of dentin-related proteins in the pulps was investigated by immunohistochemistry, using antibodies against type I collagen, dentin sialoprotein (DSP), sheathlin, and EMD. In all EMD-treated teeth a substantial amount of reparative dentin formation was observed. The amount of reparative dentin in calcium hydroxide–treated teeth was significantly smaller than in EMD-treated teeth ( P < 0.005) and was less effective in bridging the pulpal wounds. Immunohistochemistry demonstrated that enamel matrix proteins were present in detectable amounts at the application site for about 4 weeks. Moreover, the expression of proteins related to dentin formation in the wounded pulp tissue was about 2 weeks advanced in EMD-treated teeth. These findings demonstrate that enamel matrix molecules have the capacity to induce rapid pulpal wound healing in pulpotomized teeth, and suggest that the longevity and continued presence of enamel matrix macromolecules at the application site can be utilized to stimulate growth and repair of dentin over a period consistent with a favorable clinical outcome.en_US
dc.format.extent430165 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherSpringer-Verlagen_US
dc.subject.otherImmunohistochemistryen_US
dc.subject.otherEnamel Matrix Derivativeen_US
dc.subject.otherReparative Dentin Formationen_US
dc.subject.otherPulpal Wound Healingen_US
dc.subject.otherPhilosophyen_US
dc.titleImmunohistochemical Characterization of Rapid Dentin Formation Induced by Enamel Matrix Derivativeen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelDentistryen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Cariology, Restorative Sciences and Endodontics, School of Dentistry, University of Michigan, Ann Arbor, Michigan 48109-1078, USAen_US
dc.contributor.affiliationotherDepartment of Endodontics, School of Dentistry, Showa University, 2-1-1, Kitasenzoku, Ohta-ku, Tokyo 145-8515, Japanen_US
dc.contributor.affiliationotherOral Research Laboratory, Faculty of Dentistry, University of Oslo, PO box 1109, Blindern, NO-0317 Oslo, Norwayen_US
dc.contributor.affiliationotherDepartment of Endodontics, School of Dentistry, Showa University, 2-1-1, Kitasenzoku, Ohta-ku, Tokyo 145-8515, Japanen_US
dc.contributor.affiliationotherBiora AB, Medeon Science Park, Malmö SE 205-12, Swedenen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid12566040en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/48011/1/223_2003_Article_153.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/s00223-003-0153-yen_US
dc.identifier.sourceCalcified Tissue Internationalen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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