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Objectives
To investigate potential functions of transforming growth factor-beta (TGF-β) isoforms in maturation-stage ameloblasts during amelogenesis.Methods
In vivo activation of TGF-β was characterized by using matrix metalloproteinase 20 null (Mmp20-/-) and wild-type (Mmp20+/+) mice. Using mHAT9d cells cultured in the presence of each TGF-β isoform, (1) cell proliferation was determined by MTS assay, (2) immunostaining with anti-cleaved caspase-3 monoclonal antibody was performed and apoptotic indices were measured, (3) gene expression was analyzed by RT-qPCR, and (4) the uptake of amelogenin into mHAT9d cells was directly observed using a fluorescence microscope.Results
TGF-β1 and TGF-β3 were present in the enamel matrix of developing teeth which were activated by MMP20 in vivo. A genetic study revealed that the three TGF-β isoforms upregulate kallikrein 4 (KLK4) mRNA levels but downregulate carbonic anhydrase II. Moreover, TGF-β1 and TGF-β2 significantly upregulated the mRNA level of amelotin, whereas TGF-β3 dramatically downregulated the mRNA levels of odontogenic ameloblast-associated protein (ODAM), family with sequence similarity 83 member H (FAM83H), and alkaline phosphatase (ALP). Immunostaining analysis showed that the apoptosis of mHAT9d cells is induced by three TGF-β isoforms, with TGF-β3 being most effective. Both TGF-β1 and TGF-β3 induced endocytosis of amelogenin.Conclusions
We propose that TGF-β is regulated in an isoform-specific manner to perform multiple biological functions such as gene expression related to the structure of basal lamina/ameloblasts, mineral ion transport, apoptosis, and endocytosis in maturation-stage ameloblasts. 相似文献Methods: Twenty subjects participated in this study. Tooth contact during sleep was recorded using a 0.1 mm-thick polyvinyl chloride sheet called BruxChecker®. The area of the BruxChecker® in which the red dye was removed was measured. In addition, the EMG activity of the masseter muscle during sleep was recorded. The numbers of bruxism bursts and episodes were counted, and their correlations with the peeled area of the red dye on the BruxChecker® were evaluated.
Results: The number of bruxism bursts and episodes/hr significantly correlated with the peeled area at all cut-off values. The peeled area significantly correlated with the number of phasic type bruxism episodes but not with tonic or mixed type bruxism episodes.
Discussion: Since the BruxChecker® peeled area reflected phasic type sleep bruxism, the sheets may be useful in sleep bruxism screening. 相似文献