Literature DB >> 15557396

Decreased mineral content in MMP-20 null mouse enamel is prominent during the maturation stage.

J D Bartlett1, E Beniash, D H Lee, C E Smith.   

Abstract

During enamel development, matrix metalloproteinase-20 (MMP-20, enamelysin) is expressed early during the secretory stage as the enamel thickens, and kallikrein-4 (KLK-4, EMSP1) is expressed later during the maturation stage as the enamel hardens. Thus, we investigated whether the physical properties of the secretory-/maturation-stage MMP-20 null enamel were significantly different from those of controls. We demonstrated that although, in relative terms, the weight percent of mature mineral in the MMP-20 null mouse enamel was only 7-16% less than that in controls, overall the enamel mineral was reduced by about 50%, and its hardness was decreased by 37%. Percent mineral content by weight was assessed at 3 different developmental stages. Remarkably, the biggest difference in mineral content between MMP-20 null and controls occurred in the nearly mature enamel, when MMP-20 is normally no longer expressed. This suggests that MMP-20 acts either directly or indirectly to facilitate the removal of maturation-stage enamel proteins.

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Year:  2004        PMID: 15557396     DOI: 10.1177/154405910408301204

Source DB:  PubMed          Journal:  J Dent Res        ISSN: 0022-0345            Impact factor:   6.116


  42 in total

1.  Altered ion-responsive gene expression in Mmp20 null mice.

Authors:  C E Tye; R Sharma; C E Smith; J D Bartlett
Journal:  J Dent Res       Date:  2010-10-07       Impact factor: 6.116

Review 2.  Progress in matrix metalloproteinase research.

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3.  The association between genetic polymorphisms in matrix metalloproteinases and caries experience.

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Review 4.  Regulation of dental enamel shape and hardness.

Authors:  J P Simmer; P Papagerakis; C E Smith; D C Fisher; A N Rountrey; L Zheng; J C C Hu
Journal:  J Dent Res       Date:  2010-07-30       Impact factor: 6.116

5.  Matrix metalloproteinase-20 mediates dental enamel biomineralization by preventing protein occlusion inside apatite crystals.

Authors:  Saumya Prajapati; Jinhui Tao; Qichao Ruan; James J De Yoreo; Janet Moradian-Oldak
Journal:  Biomaterials       Date:  2015-10-22       Impact factor: 12.479

6.  The Presence of MMP-20 Reinforces Biomimetic Enamel Regrowth.

Authors:  S Prajapati; Q Ruan; K Mukherjee; S Nutt; J Moradian-Oldak
Journal:  J Dent Res       Date:  2017-08-28       Impact factor: 6.116

7.  Amelogenin processing by MMP-20 prevents protein occlusion inside calcite crystals.

Authors:  Keith M Bromley; Rajamani Lakshminarayanan; Mitchell Thompson; Sowmya B Lokappa; Victoria A Gallon; Kang R Cho; S Roger Qiu; Janet Moradian-Oldak
Journal:  Cryst Growth Des       Date:  2012-08-23       Impact factor: 4.076

8.  MMP20 hemopexin domain mutation in amelogenesis imperfecta.

Authors:  S-K Lee; F Seymen; H-Y Kang; K-E Lee; K Gencay; B Tuna; J-W Kim
Journal:  J Dent Res       Date:  2010-01       Impact factor: 6.116

9.  Distal cis-regulatory elements are required for tissue-specific expression of enamelin (Enam).

Authors:  Yuanyuan Hu; Petros Papagerakis; Ling Ye; Jerry Q Feng; James P Simmer; Jan C-C Hu
Journal:  Eur J Oral Sci       Date:  2008-04       Impact factor: 2.612

Review 10.  Multilevel complex interactions between genetic, epigenetic and environmental factors in the aetiology of anomalies of dental development.

Authors:  A H Brook
Journal:  Arch Oral Biol       Date:  2009-11-13       Impact factor: 2.633

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