Bourd-Boittin Katia, Fridman Rafael, Fanchon Stéphanie, Septier Dominique, Goldberg Michel, Menashi Suzanne
Matrices Extracellulaires et Biominéralisation, EA 2496, Faculté de Chirurgie Dentaire, Université René Descartes Paris V, Montrouge, France.
Exp Cell Res. 2005 Apr 1;304(2):493-505. doi: 10.1016/j.yexcr.2004.11.024. Epub 2005 Jan 11.
Organotypic cultures of embryonic mouse tooth germs were used to investigate the developmental expression and roles of MMPs in the formation and mineralization of dentin and enamel matrices. The spatially and temporally regulated expression of MMP-2, MMP-9 and MMP-20 in developing mouse tooth germs in vivo was maintained in culture. The inhibition of metalloproteinases activity by marimastat altered the morphogenesis and mineralization of the tooth germs associated with an inhibition of the activation of both MMP-20 and MMP-2. MMP inhibition deregulated the molecular processing of two major dental matrix proteins, amelogenin and dentin sialoprotein (DSP). This coincided with their accumulation and the loss of their normal distribution within the extracellular matrix, resulting in a defective mineralization of dentin and enamel matrices. These findings demonstrate the critical role of MMPs in the processing and maturation of the dental matrix.
利用胚胎小鼠牙胚的器官型培养来研究基质金属蛋白酶(MMPs)在牙本质和釉质基质形成及矿化过程中的发育表达和作用。体内发育中的小鼠牙胚中MMP-2、MMP-9和MMP-20在空间和时间上的表达调控在培养中得以维持。马里司他对金属蛋白酶活性的抑制改变了牙胚的形态发生和矿化,这与MMP-20和MMP-2激活的抑制相关。MMP抑制使两种主要牙基质蛋白,即釉原蛋白和牙本质涎蛋白(DSP)的分子加工失调。这与它们在细胞外基质中的积累以及正常分布的丧失同时发生,导致牙本质和釉质基质矿化缺陷。这些发现证明了MMPs在牙基质加工和成熟中的关键作用。