Cargando…
Enamel maturation: a brief background with implications for some enamel dysplasias
The maturation stage of enamel development begins once the final tissue thickness has been laid down. Maturation includes an initial transitional pre-stage during which morphology and function of the enamel organ cells change. When this is complete, maturation proper begins. Fully functional maturat...
Autor principal: | |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4189374/ https://www.ncbi.nlm.nih.gov/pubmed/25339913 http://dx.doi.org/10.3389/fphys.2014.00388 |
_version_ | 1782338354342264832 |
---|---|
author | Robinson, Colin |
author_facet | Robinson, Colin |
author_sort | Robinson, Colin |
collection | PubMed |
description | The maturation stage of enamel development begins once the final tissue thickness has been laid down. Maturation includes an initial transitional pre-stage during which morphology and function of the enamel organ cells change. When this is complete, maturation proper begins. Fully functional maturation stage cells are concerned with final proteolytic degradation and removal of secretory matrix components which are replaced by tissue fluid. Crystals, initiated during the secretory stage, then grow replacing the tissue fluid. Crystals grow in both width and thickness until crystals abut each other occupying most of the tissue volume i.e. full maturation. If this is not complete at eruption, a further post eruptive maturation can occur via mineral ions from the saliva. During maturation calcium and phosphate enter the tissue to facilitate crystal growth. Whether transport is entirely active or not is unclear. Ion transport is also not unidirectional and phosphate, for example, can diffuse out again especially during transition and early maturation. Fluoride and magnesium, selectively taken up at this stage can also diffuse both in an out of the tissue. Crystal growth can be compromised by excessive fluoride and by ingress of other exogenous molecules such as albumin and tetracycline. This may be exacerbated by the relatively long duration of this stage, 10 days or so in a rat incisor and up to several years in human teeth rendering this stage particularly vulnerable to ingress of foreign materials, incompletely mature enamel being the result. |
format | Online Article Text |
id | pubmed-4189374 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-41893742014-10-22 Enamel maturation: a brief background with implications for some enamel dysplasias Robinson, Colin Front Physiol Physiology The maturation stage of enamel development begins once the final tissue thickness has been laid down. Maturation includes an initial transitional pre-stage during which morphology and function of the enamel organ cells change. When this is complete, maturation proper begins. Fully functional maturation stage cells are concerned with final proteolytic degradation and removal of secretory matrix components which are replaced by tissue fluid. Crystals, initiated during the secretory stage, then grow replacing the tissue fluid. Crystals grow in both width and thickness until crystals abut each other occupying most of the tissue volume i.e. full maturation. If this is not complete at eruption, a further post eruptive maturation can occur via mineral ions from the saliva. During maturation calcium and phosphate enter the tissue to facilitate crystal growth. Whether transport is entirely active or not is unclear. Ion transport is also not unidirectional and phosphate, for example, can diffuse out again especially during transition and early maturation. Fluoride and magnesium, selectively taken up at this stage can also diffuse both in an out of the tissue. Crystal growth can be compromised by excessive fluoride and by ingress of other exogenous molecules such as albumin and tetracycline. This may be exacerbated by the relatively long duration of this stage, 10 days or so in a rat incisor and up to several years in human teeth rendering this stage particularly vulnerable to ingress of foreign materials, incompletely mature enamel being the result. Frontiers Media S.A. 2014-10-08 /pmc/articles/PMC4189374/ /pubmed/25339913 http://dx.doi.org/10.3389/fphys.2014.00388 Text en Copyright © 2014 Robinson. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Physiology Robinson, Colin Enamel maturation: a brief background with implications for some enamel dysplasias |
title | Enamel maturation: a brief background with implications for some enamel dysplasias |
title_full | Enamel maturation: a brief background with implications for some enamel dysplasias |
title_fullStr | Enamel maturation: a brief background with implications for some enamel dysplasias |
title_full_unstemmed | Enamel maturation: a brief background with implications for some enamel dysplasias |
title_short | Enamel maturation: a brief background with implications for some enamel dysplasias |
title_sort | enamel maturation: a brief background with implications for some enamel dysplasias |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4189374/ https://www.ncbi.nlm.nih.gov/pubmed/25339913 http://dx.doi.org/10.3389/fphys.2014.00388 |
work_keys_str_mv | AT robinsoncolin enamelmaturationabriefbackgroundwithimplicationsforsomeenameldysplasias |