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Kallikrein-related peptidase-4 (KLK4): role in enamel formation and revelations from ablated mice

Enamel development occurs in stages. During the secretory stage, a soft protein rich enamel layer is produced that expands to reach its final thickness. During the maturation stage, proteins are removed and the enamel matures into the hardest substance in the body. KLK4 is expressed during the trans...

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Autores principales: Bartlett, John D., Simmer, James P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4082239/
https://www.ncbi.nlm.nih.gov/pubmed/25071586
http://dx.doi.org/10.3389/fphys.2014.00240
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author Bartlett, John D.
Simmer, James P.
author_facet Bartlett, John D.
Simmer, James P.
author_sort Bartlett, John D.
collection PubMed
description Enamel development occurs in stages. During the secretory stage, a soft protein rich enamel layer is produced that expands to reach its final thickness. During the maturation stage, proteins are removed and the enamel matures into the hardest substance in the body. KLK4 is expressed during the transition from secretory to the maturation stage and its expression continues throughout maturation. KLK4 is a glycosylated chymotrypsin-like serine protease that cleaves enamel matrix proteins prior to their export out of the hardening enamel layer. Mutations in KLK4 can cause autosomal recessive, non-syndromic enamel malformations in humans and mice. Klk4 ablated mice initially have normal-looking teeth with enamel of full thickness. However, the enamel is soft and protein-rich. Three findings are notable from Klk4 ablated mice: first, enamel rods fall from the interrod enamel leaving behind empty holes where the enamel fractures near the underlying dentin surface. Second, the ~10,000 crystallites that normally fuse to form a solid enamel rod fail to grow together in the ablated mice and can fall out of the rods. Third, and most striking, the crystallites grow substantially in width and thickness (a- and b-axis) in the ablated mice until they almost interlock. The crystallites grow in defined enamel rods, but interlocking is prevented presumably because too much protein remains. Conventional thought holds that enamel proteins bind specifically to the sides of enamel crystals to inhibit growth in width and thickness so that the thin, ribbon-like enamel crystallites grow predominantly in length. Results from Klk4 ablated mice demonstrate that this convention requires updating. An alternative mechanism is proposed whereby enamel proteins serve to form a mold or support structure that shapes and orients the mineral ribbons as they grow in length. The remnants of this support structure must be removed by KLK4 so that the crystallites can interlock to form fully hardened enamel.
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spelling pubmed-40822392014-07-28 Kallikrein-related peptidase-4 (KLK4): role in enamel formation and revelations from ablated mice Bartlett, John D. Simmer, James P. Front Physiol Physiology Enamel development occurs in stages. During the secretory stage, a soft protein rich enamel layer is produced that expands to reach its final thickness. During the maturation stage, proteins are removed and the enamel matures into the hardest substance in the body. KLK4 is expressed during the transition from secretory to the maturation stage and its expression continues throughout maturation. KLK4 is a glycosylated chymotrypsin-like serine protease that cleaves enamel matrix proteins prior to their export out of the hardening enamel layer. Mutations in KLK4 can cause autosomal recessive, non-syndromic enamel malformations in humans and mice. Klk4 ablated mice initially have normal-looking teeth with enamel of full thickness. However, the enamel is soft and protein-rich. Three findings are notable from Klk4 ablated mice: first, enamel rods fall from the interrod enamel leaving behind empty holes where the enamel fractures near the underlying dentin surface. Second, the ~10,000 crystallites that normally fuse to form a solid enamel rod fail to grow together in the ablated mice and can fall out of the rods. Third, and most striking, the crystallites grow substantially in width and thickness (a- and b-axis) in the ablated mice until they almost interlock. The crystallites grow in defined enamel rods, but interlocking is prevented presumably because too much protein remains. Conventional thought holds that enamel proteins bind specifically to the sides of enamel crystals to inhibit growth in width and thickness so that the thin, ribbon-like enamel crystallites grow predominantly in length. Results from Klk4 ablated mice demonstrate that this convention requires updating. An alternative mechanism is proposed whereby enamel proteins serve to form a mold or support structure that shapes and orients the mineral ribbons as they grow in length. The remnants of this support structure must be removed by KLK4 so that the crystallites can interlock to form fully hardened enamel. Frontiers Media S.A. 2014-07-04 /pmc/articles/PMC4082239/ /pubmed/25071586 http://dx.doi.org/10.3389/fphys.2014.00240 Text en Copyright © 2014 Bartlett and Simmer. http://creativecommons.org/licenses/by/3.0/ 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
Bartlett, John D.
Simmer, James P.
Kallikrein-related peptidase-4 (KLK4): role in enamel formation and revelations from ablated mice
title Kallikrein-related peptidase-4 (KLK4): role in enamel formation and revelations from ablated mice
title_full Kallikrein-related peptidase-4 (KLK4): role in enamel formation and revelations from ablated mice
title_fullStr Kallikrein-related peptidase-4 (KLK4): role in enamel formation and revelations from ablated mice
title_full_unstemmed Kallikrein-related peptidase-4 (KLK4): role in enamel formation and revelations from ablated mice
title_short Kallikrein-related peptidase-4 (KLK4): role in enamel formation and revelations from ablated mice
title_sort kallikrein-related peptidase-4 (klk4): role in enamel formation and revelations from ablated mice
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4082239/
https://www.ncbi.nlm.nih.gov/pubmed/25071586
http://dx.doi.org/10.3389/fphys.2014.00240
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