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- Publisher Website: 10.1080/03008200390181816
- Scopus: eid_2-s2.0-0037240958
- PMID: 12952213
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Article: Delayed tooth eruption in membrane type-1 matrix metalloproteinase deficient mice
Title | Delayed tooth eruption in membrane type-1 matrix metalloproteinase deficient mice |
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Authors | |
Keywords | Biomineralization Dental Enamel Dentin Development Matrix metalloproteinase |
Issue Date | 2003 |
Publisher | Informa Healthcare. The Journal's web site is located at http://www.tandf.co.uk/journals/titles/03008207.asp |
Citation | Connective Tissue Research, 2003, v. 44 SUPPL. 1, p. 300-304 How to Cite? |
Abstract | Membrane-type 1 matrix metalloproteinase (MT1-MMP) is expressed highly in mineralizing tissues including bones and teeth. Mice deficient in MT1-MMP (-/-) display severe defects in skeletal development including dwarfism, osteopenia, and craniofacial abnormalities. Death occurs in these mice by about 3 weeks of age. Since MT1-MMP is expressed by the ameloblasts of the enamel organ and by the odontoblasts of the dental papilla, we asked if the developing teeth were adversely affected in the knockout animals. Molars from MT1-MMP -/- mice and controls were examined by histological, X-ray, and SEM analysis at 4, 18-20, and 25 days of postnatal development. At 4 days of development the molars from the -/- mice appeared histologically normal. At 18-20 days of development, the first molars of the -/- mice had apparently normal tooth crowns with normal dentin and enamel; however, the roots were truncated and the teeth had not yet erupted. In contrast to the -/- mice, the first molars of the 18-20-day control animals had erupted. SEM analysis of a -/- first molar and incisor revealed a normal enamel prism pattern. However, X-ray analysis demonstrated that tooth eruption was delayed by approximately 5 days and that the tooth roots were abnormally short in the knockout animals. Since MT1-MMP-deficient mice have been demonstrated to display a generalized increase in bone resorption, these data suggest that inefficient growth of bone surrounding the tooth root complex causes a delay in tooth eruption. |
Persistent Identifier | http://hdl.handle.net/10722/68000 |
ISSN | 2023 Impact Factor: 2.8 2023 SCImago Journal Rankings: 0.750 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Bartlett, JD | en_HK |
dc.contributor.author | Zhou, Z | en_HK |
dc.contributor.author | Skobe, Z | en_HK |
dc.contributor.author | Dobeck, JM | en_HK |
dc.contributor.author | Tryggvason, K | en_HK |
dc.date.accessioned | 2010-09-06T06:00:22Z | - |
dc.date.available | 2010-09-06T06:00:22Z | - |
dc.date.issued | 2003 | en_HK |
dc.identifier.citation | Connective Tissue Research, 2003, v. 44 SUPPL. 1, p. 300-304 | en_HK |
dc.identifier.issn | 0300-8207 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/68000 | - |
dc.description.abstract | Membrane-type 1 matrix metalloproteinase (MT1-MMP) is expressed highly in mineralizing tissues including bones and teeth. Mice deficient in MT1-MMP (-/-) display severe defects in skeletal development including dwarfism, osteopenia, and craniofacial abnormalities. Death occurs in these mice by about 3 weeks of age. Since MT1-MMP is expressed by the ameloblasts of the enamel organ and by the odontoblasts of the dental papilla, we asked if the developing teeth were adversely affected in the knockout animals. Molars from MT1-MMP -/- mice and controls were examined by histological, X-ray, and SEM analysis at 4, 18-20, and 25 days of postnatal development. At 4 days of development the molars from the -/- mice appeared histologically normal. At 18-20 days of development, the first molars of the -/- mice had apparently normal tooth crowns with normal dentin and enamel; however, the roots were truncated and the teeth had not yet erupted. In contrast to the -/- mice, the first molars of the 18-20-day control animals had erupted. SEM analysis of a -/- first molar and incisor revealed a normal enamel prism pattern. However, X-ray analysis demonstrated that tooth eruption was delayed by approximately 5 days and that the tooth roots were abnormally short in the knockout animals. Since MT1-MMP-deficient mice have been demonstrated to display a generalized increase in bone resorption, these data suggest that inefficient growth of bone surrounding the tooth root complex causes a delay in tooth eruption. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Informa Healthcare. The Journal's web site is located at http://www.tandf.co.uk/journals/titles/03008207.asp | en_HK |
dc.relation.ispartof | Connective Tissue Research | en_HK |
dc.rights | Connective Tissue Research. Copyright © Informa Healthcare. | en_HK |
dc.subject | Biomineralization | - |
dc.subject | Dental Enamel | - |
dc.subject | Dentin | - |
dc.subject | Development | - |
dc.subject | Matrix metalloproteinase | - |
dc.subject.mesh | Animals | en_HK |
dc.subject.mesh | Animals, Newborn | en_HK |
dc.subject.mesh | Calcification, Physiologic - physiology | en_HK |
dc.subject.mesh | Dental Enamel - enzymology - ultrastructure | en_HK |
dc.subject.mesh | Matrix Metalloproteinase 14 | en_HK |
dc.subject.mesh | Matrix Metalloproteinases, Membrane-Associated | en_HK |
dc.subject.mesh | Metalloendopeptidases - deficiency - genetics - metabolism | en_HK |
dc.subject.mesh | Mice | en_HK |
dc.subject.mesh | Mice, Knockout | en_HK |
dc.subject.mesh | Microscopy, Electron, Scanning | en_HK |
dc.subject.mesh | Molar - enzymology - growth & development - pathology | en_HK |
dc.subject.mesh | Tooth Eruption - physiology | en_HK |
dc.subject.mesh | Tooth Root - growth & development - pathology | en_HK |
dc.title | Delayed tooth eruption in membrane type-1 matrix metalloproteinase deficient mice | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0300-8207&volume=44&issue=Suppl 1&spage=1&epage=5&date=2003&atitle=Delayed+Tooth+Eruption+in+Membrane+Type-1+Matrix+Metalloproteinase+Deficient+Mice++++ | en_HK |
dc.identifier.email | Zhou, Z:zhongjun@hkucc.hku.hk | en_HK |
dc.identifier.authority | Zhou, Z=rp00503 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1080/03008200390181816 | - |
dc.identifier.pmid | 12952213 | - |
dc.identifier.scopus | eid_2-s2.0-0037240958 | en_HK |
dc.identifier.hkuros | 84066 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-0037240958&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 44 | en_HK |
dc.identifier.issue | SUPPL. 1 | en_HK |
dc.identifier.spage | 300 | en_HK |
dc.identifier.epage | 304 | en_HK |
dc.identifier.isi | WOS:000181811000050 | - |
dc.publisher.place | United Kingdom | en_HK |
dc.identifier.scopusauthorid | Bartlett, JD=26323989100 | en_HK |
dc.identifier.scopusauthorid | Zhou, Z=8631856300 | en_HK |
dc.identifier.scopusauthorid | Skobe, Z=7004153003 | en_HK |
dc.identifier.scopusauthorid | Dobeck, JM=6602959469 | en_HK |
dc.identifier.scopusauthorid | Tryggvason, K=7102025185 | en_HK |
dc.identifier.issnl | 0300-8207 | - |