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Endocytosis and Enamel Formation
Enamel formation requires consecutive stages of development to achieve its characteristic extreme mineral hardness. Mineralization depends on the initial presence then removal of degraded enamel proteins from the matrix via endocytosis. The ameloblast membrane resides at the interface between matrix...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5534449/ https://www.ncbi.nlm.nih.gov/pubmed/28824442 http://dx.doi.org/10.3389/fphys.2017.00529 |
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author | Pham, Cong-Dat Smith, Charles E. Hu, Yuanyuan Hu, Jan C-C. Simmer, James P. Chun, Yong-Hee P. |
author_facet | Pham, Cong-Dat Smith, Charles E. Hu, Yuanyuan Hu, Jan C-C. Simmer, James P. Chun, Yong-Hee P. |
author_sort | Pham, Cong-Dat |
collection | PubMed |
description | Enamel formation requires consecutive stages of development to achieve its characteristic extreme mineral hardness. Mineralization depends on the initial presence then removal of degraded enamel proteins from the matrix via endocytosis. The ameloblast membrane resides at the interface between matrix and cell. Enamel formation is controlled by ameloblasts that produce enamel in stages to build the enamel layer (secretory stage) and to reach final mineralization (maturation stage). Each stage has specific functional requirements for the ameloblasts. Ameloblasts adopt different cell morphologies during each stage. Protein trafficking including the secretion and endocytosis of enamel proteins is a fundamental task in ameloblasts. The sites of internalization of enamel proteins on the ameloblast membrane are specific for every stage. In this review, an overview of endocytosis and trafficking of vesicles in ameloblasts is presented. The pathways for internalization and routing of vesicles are described. Endocytosis is proposed as a mechanism to remove debris of degraded enamel protein and to obtain feedback from the matrix on the status of the maturing enamel. |
format | Online Article Text |
id | pubmed-5534449 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-55344492017-08-18 Endocytosis and Enamel Formation Pham, Cong-Dat Smith, Charles E. Hu, Yuanyuan Hu, Jan C-C. Simmer, James P. Chun, Yong-Hee P. Front Physiol Physiology Enamel formation requires consecutive stages of development to achieve its characteristic extreme mineral hardness. Mineralization depends on the initial presence then removal of degraded enamel proteins from the matrix via endocytosis. The ameloblast membrane resides at the interface between matrix and cell. Enamel formation is controlled by ameloblasts that produce enamel in stages to build the enamel layer (secretory stage) and to reach final mineralization (maturation stage). Each stage has specific functional requirements for the ameloblasts. Ameloblasts adopt different cell morphologies during each stage. Protein trafficking including the secretion and endocytosis of enamel proteins is a fundamental task in ameloblasts. The sites of internalization of enamel proteins on the ameloblast membrane are specific for every stage. In this review, an overview of endocytosis and trafficking of vesicles in ameloblasts is presented. The pathways for internalization and routing of vesicles are described. Endocytosis is proposed as a mechanism to remove debris of degraded enamel protein and to obtain feedback from the matrix on the status of the maturing enamel. Frontiers Media S.A. 2017-07-31 /pmc/articles/PMC5534449/ /pubmed/28824442 http://dx.doi.org/10.3389/fphys.2017.00529 Text en Copyright © 2017 Pham, Smith, Hu, Hu, Simmer and Chun. 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 Pham, Cong-Dat Smith, Charles E. Hu, Yuanyuan Hu, Jan C-C. Simmer, James P. Chun, Yong-Hee P. Endocytosis and Enamel Formation |
title | Endocytosis and Enamel Formation |
title_full | Endocytosis and Enamel Formation |
title_fullStr | Endocytosis and Enamel Formation |
title_full_unstemmed | Endocytosis and Enamel Formation |
title_short | Endocytosis and Enamel Formation |
title_sort | endocytosis and enamel formation |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5534449/ https://www.ncbi.nlm.nih.gov/pubmed/28824442 http://dx.doi.org/10.3389/fphys.2017.00529 |
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