Noggin Is Required for Early Development of Murine Upper Incisors

被引:21
作者
Hu, X. [1 ]
Wang, Y. [2 ,3 ]
He, F. [3 ]
Li, L. [3 ]
Zheng, Y. [3 ]
Zhang, Y. [1 ]
Chen, Y. P. [1 ,3 ]
机构
[1] Fujian Normal Univ, Coll Life Sci, Fujian Key Lab Dev & Neuro Biol, Fuzhou, Fujian Province, Peoples R China
[2] Fourth Mil Med Univ, Coll Stomatol, Dept Operat Dent & Endodont, Xian 710032, Shaangxi, Peoples R China
[3] Tulane Univ, Dept Cell & Mol Biol, New Orleans, LA 70118 USA
基金
中国国家自然科学基金;
关键词
BMP antagonist; BMP homeostasis; Chordin; Gremlin; tooth development; tooth fusion; BONE MORPHOGENETIC PROTEINS; ECTOPIC EXPRESSION; TOOTH; BMP4; MSX1; INHIBITION; MECHANISM; OUTGROWTH; HEDGEHOG; CHORDIN;
D O I
10.1177/0022034511435939
中图分类号
R78 [口腔科学];
学科分类号
100302 [口腔临床医学];
摘要
BMP signaling plays crucial roles in the development of many organs, including the tooth. Equally important is BMP signaling homeostasis, as demonstrated by multiple organ defects in mice lacking the extracellular BMP antagonist Noggin. Here, we show that Noggin is initially expressed in the maxillary mesenchyme adjunct to the upper incisor at the initiation stage, and then in the developing teeth, including incisors and molars, from the bud stage. Noggin mutants develop normal molars and mandibular incisors, but form a single, medially located upper incisor that is arrested at the late bud stage. Histological and molecular marker analyses demonstrated that two distinct upper incisor placodes initiate independently at E11.5, but begin to fuse at E12.5, coupling with elevated cell proliferation rates in the developing tooth germs. We further found that Chordin and Gremlin, two other BMP antagonists, are co-expressed with Noggin in the developing lower incisor and molar teeth. These observations indicate the importance of BMP signaling homeostasis, and suggest a functional redundancy between BMP antagonists during tooth development.
引用
收藏
页码:394 / 400
页数:7
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