Literature DB >> 9881602

Expression and localization of membrane type 1 matrix metalloproteinase in tooth tissues.

C Caron1, J Xue, J D Bartlett.   

Abstract

Matrix metalloproteinases (MMPs) have been detected in forming dental enamel and are thought to play an important role during enamel biomineralization. Membrane-type 1 matrix metalloproteinase (MT1-MMP) is a membrane bound member of the MMP gene family that has previously been shown to be expressed by cells associated with bone and cartilage formation (osteoclasts, osteoblasts and chondrocytes). Thus, we asked if MT1-MMP was also expressed by the cells responsible for the formation of enamel and dentin. A porcine MT1-MMP cDNA composed of 3284 bp was isolated from an enamel organ-specific cDNA library. Multiple tissue Northern blot analysis revealed that the MT1-MMP message was expressed highly in the enamel organ and pulp organ when compared to the expression levels observed in other non-mineralizing tissues. Northern blot analysis of stage-specific enamel organs (early secretory, late secretory, or maturation stage) and their corresponding pulp organs revealed that MT1-MMP expression increased as the dentin matured. In the enamel organs, however, the MT1-MMP message level became reduced only during the late secretory stage. Immunohistochemical analysis showed that MT1-MMP was present on the surface of the cells (ameloblasts and odontoblasts) responsible for dentin and enamel formation. Thus, MT1-MMP is highly expressed in developing tooth tissues and may play a role in the biomineralization of enamel and dentin.

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Year:  1998        PMID: 9881602     DOI: 10.1016/s0945-053x(98)90098-1

Source DB:  PubMed          Journal:  Matrix Biol        ISSN: 0945-053X            Impact factor:   11.583


  7 in total

1.  Fluoride does not inhibit enamel protease activity.

Authors:  C E Tye; J V Antone; J D Bartlett
Journal:  J Dent Res       Date:  2010-11-30       Impact factor: 6.116

2.  MT1-MMP expression in the odontogenic region of rat incisors undergoing interrupted eruption.

Authors:  Nádia Fayez Omar; José Rosa Gomes; Juliana dos Santos Neves; Cristiane Ribeiro Salmon; Pedro Duarte Novaes
Journal:  J Mol Histol       Date:  2011-09-10       Impact factor: 2.611

3.  Increase of MT1-MMP, TIMP-2 and Ki-67 proteins in the odontogenic region of the rat incisor post-shortening procedure.

Authors:  Jose Rosa Gomes; Nádia Fayez Omar; Juliana Dos Santos Neves; Eliene Aparecida Orsini Narvaes; Pedro Duarte Novaes
Journal:  J Mol Histol       Date:  2010-09-21       Impact factor: 2.611

4.  Immunolocalization and activity of the MMP-9 and MMP-2 in odontogenic region of the rat incisor tooth after post shortening procedure.

Authors:  Jose Rosa Gomes; Nádia Fayez Omar; Juliana dos Santos Neves; Eliene Aparecida Orsini Narvaes; Pedro Duarte Novaes
Journal:  J Mol Histol       Date:  2011-02-10       Impact factor: 2.611

5.  Immunocytochemical and biochemical detection of EMMPRIN in the rat tooth germ: differentiation-dependent co-expression with MMPs and co-localization with caveolin-1 in membrane rafts of dental epithelial cells.

Authors:  W Schwab; H Harada; W Goetz; M Nowicki; M Witt; M Kasper; K Barth
Journal:  Histochem Cell Biol       Date:  2007-08-08       Impact factor: 4.304

Review 6.  Dental enamel development: proteinases and their enamel matrix substrates.

Authors:  John D Bartlett
Journal:  ISRN Dent       Date:  2013-09-16

7.  Genetic Association of MMP10, MMP14, and MMP16 with Dental Caries.

Authors:  D D Lewis; J R Shaffer; E Feingold; M Cooper; M M Vanyukov; B S Maher; R L Slayton; M C Willing; S E Reis; D W McNeil; R J Crout; R J Weyant; S M Levy; A R Vieira; M L Marazita
Journal:  Int J Dent       Date:  2017-02-28
  7 in total

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