Literature DB >> 23684768

Establishment of crown-root domain borders in mouse incisor.

Emma Juuri1, Kan Saito, Sylvie Lefebvre, Frederic Michon.   

Abstract

Teeth are composed of two domains, the enamel-covered crown and the enamel-free root. The understanding of the initiation and regulation of crown and root domain formation is important for the development of bioengineered teeth. In most teeth the crown develops before the root, and erupts to the oral cavity whereas the root anchors the tooth to the jawbone. However, in the continuously growing mouse incisor the crown and root domains form simultaneously, the crown domain forming the labial and the root domain the lingual part of the tooth. While the crown-root border on the incisor distal side supports the distal enamel extent, reflecting an evolutionary diet adaptation, on the incisor mesial side the root-like surface is necessary for the attachment of the interdental ligament between the two incisors. Therefore, the mouse incisor exhibits a functional distal-mesial asymmetry. Here, we used the mouse incisor as a model to understand the mechanisms involved in the crown-root border formation. We analyzed the cellular origins and gene expression patterns leading to the development of the mesial and distal crown-root borders. We discovered that Barx2, En1, Wnt11, and Runx3 were exclusively expressed on the mesial crown-root border. In addition, the distal border of the crown-root domain might be established by cells from a different origin and by an early Follistatin expression, factor known to be involved in the root domain formation. The use of different mechanisms to establish domain borders gives indications of the incisor functional asymmetry.
Copyright © 2013 Elsevier B.V. All rights reserved.

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Year:  2013        PMID: 23684768     DOI: 10.1016/j.gep.2013.05.001

Source DB:  PubMed          Journal:  Gene Expr Patterns        ISSN: 1567-133X            Impact factor:   1.224


  2 in total

1.  Plasticity within the niche ensures the maintenance of a Sox2+ stem cell population in the mouse incisor.

Authors:  Maria Sanz-Navarro; Kerstin Seidel; Zhao Sun; Ludivine Bertonnier-Brouty; Brad A Amendt; Ophir D Klein; Frederic Michon
Journal:  Development       Date:  2018-01-08       Impact factor: 6.868

2.  Mutant GDF5 enhances ameloblast differentiation via accelerated BMP2-induced Smad1/5/8 phosphorylation.

Authors:  Jia Liu; Kan Saito; Yuriko Maruya; Takashi Nakamura; Aya Yamada; Emiko Fukumoto; Momoko Ishikawa; Tsutomu Iwamoto; Kanako Miyazaki; Keigo Yoshizaki; Lihong Ge; Satoshi Fukumoto
Journal:  Sci Rep       Date:  2016-03-31       Impact factor: 4.379

  2 in total

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