Post-natal Effect of Overexpressed DKK1 on Mandibular Molar Formation

被引:50
作者
Han, X. L. [1 ,2 ]
Liu, M. [3 ]
Voisey, A. [1 ]
Ren, Y. S. [1 ]
Kurimoto, P. [3 ]
Gao, T. [1 ]
Tefera, L. [1 ]
Dechow, P. [1 ]
Ke, H. Z. [3 ]
Feng, J. Q. [1 ]
机构
[1] Texas A&M Hlth Sci Ctr, Baylor Coll Dent, Dept Biomed Sci, Dallas, TX 75246 USA
[2] Sichuan Univ, State Key Lab Oral Dis, W China Stomatol Hosp, Chengdu 610064, Sichuan, Peoples R China
[3] Amgen Inc, Dept Metab Disorders, Thousand Oaks, CA 91320 USA
基金
美国国家卫生研究院; 中国国家自然科学基金;
关键词
DKK1; tooth development; odontoblast; mandibular molar; transgenic mice; dentinogenesis; TOOTH MORPHOGENESIS; HEAD INDUCTION; IN-VIVO; EXPRESSION; MOUSE; BONE; DICKKOPF-1; DENTITION; NESTIN; ROLES;
D O I
10.1177/0022034511421926
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Dickkopf-related protein 1 (DKK1) is a potent inhibitor of Wnt/beta-catenin signaling. Dkk1-null mutant embryos display severe defects in head induction. Conversely, targeted expression of Dkk1 in dental epithelial cells leads to the formation of dysfunctional enamel knots and subsequent tooth defects during embryonic development. However, its role in post-natal dentinogenesis is largely unknown. To address this issue, we studied the role of DKK1 in post-natal dentin development using 2.3-kb Colla1-Dkk1 transgenic mice, with the following key findings: (1) The Dkk1 transgene was highly expressed in pulp and odontoblast cells during post-natal developmental stages; (2) the 1(st) molar displayed short roots, an enlarged pulp/root canal region, and a decrease in the dentin formation rate; (3) a small malformed second molar and an absent third molar; (4) an increase of immature odontoblasts, few mature odontoblasts, and sharply reduced dentinal tubules; and (5) a dramatic change in Osx and nestin expression. We propose that DKK1 controls post-natal mandibular molar dentin formation either directly or indirectly via the inhibition of Wnt signaling at the following aspects: (i) post-natal dentin formation, (ii) formation and/or maintenance of the dentin tubular system, (iii) mineralization of the dentin, and (iv) regulation of molecules such as Osx and nestin.
引用
收藏
页码:1312 / 1317
页数:6
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