Catón Javier, Bringas Pablo, Zeichner-David Margarita
Center for Craniofacial Molecular Biology, University of Southern California School of Dentistry, 2250 Alcazar St., CSA 106, Los Angeles, CA 90033, USA.
Arch Oral Biol. 2005 Feb;50(2):123-9. doi: 10.1016/j.archoralbio.2004.11.012. Epub 2005 Jan 12.
Insulin-like growth factors (IGF-I and IGF-II) have been shown to play an important role in growth and differentiation in a number of tissues including mineralizing bone. Little is known about their role in tooth mineralization. Previous work in our laboratory has shown the presence of IGFs ligands, their receptors, and their binding proteins during mouse tooth morphogenesis. The expression of IGF I coincides with the expression of amelogenin, ameloblastin and enamelin at the late bell and secretory stage. The objective of this study is to determine the mechanisms by which IGFs modulate enamel and dentin formation. Mouse first mandibular molars were dissected from E16 and E17 mouse embryos and placed in organ culture in the presence of IGF-I or IGF-II. The molars were harvested after 12 days for histological examination or 1 day for mRNA expression analysis by real-time RT-PCR. Our results show an increase in enamel deposition, and an induction of enamelin, amelogenin and collagen type I mRNA expression, while expression of DSPP was down-regulated. These results suggest that IGFs increase enamel formation by the induction of gene expression of enamel related genes. Studies are underway to determine a possible mechanism for these factors.
胰岛素样生长因子(IGF-I和IGF-II)已被证明在包括矿化骨在内的许多组织的生长和分化中发挥重要作用。关于它们在牙齿矿化中的作用知之甚少。我们实验室之前的工作表明,在小鼠牙齿形态发生过程中存在IGF配体、它们的受体及其结合蛋白。IGF I的表达与成釉蛋白、成釉细胞蛋白和釉原蛋白在钟状期末期和分泌期的表达一致。本研究的目的是确定IGF调节釉质和牙本质形成的机制。从E16和E17小鼠胚胎中解剖出小鼠第一下颌磨牙,并在存在IGF-I或IGF-II的情况下进行器官培养。12天后收获磨牙进行组织学检查,或1天后收获进行实时RT-PCR分析mRNA表达。我们的结果显示釉质沉积增加,釉原蛋白、成釉蛋白和I型胶原mRNA表达诱导,而DSPP表达下调。这些结果表明,IGF通过诱导釉质相关基因的基因表达来增加釉质形成。正在进行研究以确定这些因素的可能机制。