TGFβ1 signaling and stimulation of osteoadherin in human odontoblasts in vitro

被引:33
|
作者
Lucchini, M [1 ]
Romeas, A [1 ]
Couble, ML [1 ]
Bleicher, F [1 ]
Magloire, H [1 ]
Farges, JC [1 ]
机构
[1] Fac Odontol, Lab Dev Dent Tissues, EA 1892, F-69372 Lyon 08, France
关键词
transforming growth factor beta; SMAD proteins; keratan sulfate proteoglycan; tooth; dentin matrix;
D O I
10.1080/030085200290000790
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Transforming growth factor beta 1 (TGFbeta1) is generally considered to be a potent inducer of dentin formation. In order to further assess this role, we studied the influence of this factor in human dental pulp cells on the expression of osteoadherin (OSAD), a newly described proteoglycan found in bone and dentin and suspected to play a role in mineralization events. We performed TGFbeta1 stimulation both in cultures of human tooth thick slices including mature odontoblasts and in pulp explant cultures giving rise to early secretory odontoblasts or pulpal fibroblasts. We first showed by immunohistochemistry that molecules involved in TGFbeta1 signal transduction, that is, membrane receptors TbetaRI and TbetaRII and intracellular proteins SMAD-2, SMAD-3, and SMAD-4, were present in human dental cells in vivo and were all maintained after culture of thick-sliced teeth in cells undergoing TGFbeta1 stimulation. In this culture system, OSAD synthesis was increased in mature odontoblasts close to the TGFbeta1 delivery system. In explant cultures, semiquantitative reverse-transcription polymerase chain reaction (RT-PCR) analysis indicated that the growth factor stimulated OSAD gene expression in early secretory odontoblasts and in pulpal fibroblasts. Taken together, these results indicate that OSAD expression is stimulated by TGFbeta1 in pulpal fibroblasts and in early secretory and mature odontoblasts. We suggest that TGFbeta1 in this way could control the organization and the mineralization of the extracellular matrix deposited by these cells during dentin formation.
引用
收藏
页码:345 / 353
页数:9
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