ABSTRACT
Cleft palate has been studied with epidemiologic and molecular methods, and many etiologic factors have been examined closely. Among the research methods, biologic molecule research has been the most important method for cleft palate formation study. The TGF-beta played an important role in cell migration, epithelial-mesenchymal transdifferentiation, extracellular matrix synthesis and deposition. But there was not much research on the correlation cleft palate induced by beta-aminonitroproprionitrile(BAPN) and TGF-beta expression. The purpose of the present study was to examine how TGF-beta is expressed in cleft palate rats. 4 Timed-pregnant Sprague-Dawley rats were obtained on the 10th gestation day. On the 13th day of gestation, BAPN-monofumarate salts ((C3H6N2)2.C4H4O4) were individually, orally administered to 3 pregnant rats at a ratio of 1g/kg body weight. And 4 pregnant rats were sacrificed on day 20 post coitus (p.c.). The TGF-beta expression in the cleft formed rats fetuses showed the following patterns : 1. Osteoblast and mesenchymal cells of the cleft palate rats were of low expression compared with those of the control rats. 2. The cleft palate rats didn't show any difference in the TGF-beta expression of osteocyte from the control rats. 3. In western blot analysis, the thickness of band of TGF-beta in the cleft palate rats was thinner and more diluted than that of the control rats.
Subject(s)
Animals , Pregnancy , Rats , Aminopropionitrile , Blotting, Western , Body Weight , Cell Movement , Cleft Palate , Coitus , Extracellular Matrix , Fetus , Osteoblasts , Osteocytes , Rats, Sprague-Dawley , Salts , Transforming Growth Factor betaABSTRACT
The purpose of this study was to investigate osteonectin expression patterns in cleft palatecompare to normal palate rats. We used 4 pregnant rats, and beta-aminoproprionitrile was oral dose to rat according to lg/kg body weight at gestation days 13 to induce cleft palate. Total 6 fetus was got with cleft formed, then 3 fetus was used for immunohistostain and 3 fetus was used for western blot analysis. Expression patterns of osteonectin in mesenchymal cells of cleft palate was more dilute to mesenchymal cells of normal palate with immnunohistostain, and width and length of band of maxilla in cleft palate was more thin than maxilla of normal palate with western blot study.