Dynamic analysis of the expression of the TGFβ/SMAD2 pathway and CCN2/CTGF during early steps of tooth development

被引:16
作者
Pacheco, Marcos S. [1 ]
Reis, Alice H. [1 ]
Aguiar, Diego P. [1 ]
Lyons, Karen M. [2 ]
Abreu, Jose G. [1 ]
机构
[1] Univ Fed Rio de Janeiro, Inst Ciencias Biomed, Dept Anat, BR-21949590 Rio De Janeiro, Brazil
[2] Univ Calif Los Angeles, Dept Orthoped Surg, Dept Mol Cell & Dev Biol, Los Angeles, CA USA
关键词
Ccn2 null mouse; CTGF/CCN2; growth factor; epithelium-mesenchyme interaction; TGF beta/SMAD2; odontogenesis;
D O I
10.1159/000112640
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Background/Aims: CCN2 is present during tooth development. However, the relationship between CCN2 and the transforming growth factor beta (TGF beta)/SMAD2/3 signaling cascade during early stages of tooth development is unclear. Here, we compare the expression of CCN2 and TGF beta/SMAD2/3 components during tooth development, and analyze the functioning of TGF beta/SMAD2/3 in wild-type (WT) and Ccn2 null (Ccn2(-/-)) mice. Methods: Coronal sections of mice on embryonic day ( E) 11.5, E12.5, E13.5, E14.5 and E18.5 from WT and Ccn2(-/-) were immunoreacted to detect CCN2 and components of the TGF beta signaling pathway and assayed for 5 '-bromo-2 '-deoxyuridine immunolabeling and proliferating cell nuclear antigen immunostaining. Results: CCN2 and TGF beta signaling components such as TGF beta 1, TGF beta receptor II, SMADs2/3 and SMAD4 were expressed in inducer tissues during early stages of tooth development. Proliferation analysis in these areas showed that epithelial cells proliferate less than mesenchymal cells from E11.5 to E13.5, while at E14.5 they proliferate more than mesenchymal cells. We did not find a correlation between functioning of the TGF beta 1 cascade and CCN2 expression because Ccn2(-/-) mice showed neither a reduction in SMAD2 phosphorylation nor a difference in cell proliferation. Conclusion: CCN2 and the TGF beta/SMAD2/3 signaling pathway are active in signaling centers of tooth development where proliferation is dynamic, but these mechanisms may act independently. Copyright (c) 2007 S. Karger AG, Basel.
引用
收藏
页码:199 / 210
页数:12
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