Sasano Yasuyuki, Nakamura Megumi, Henmi Akiko, Okata Hiroshi, Suzuki Osamu, Kayaba Atsuko, Mayanagi Miyuki
Division of Craniofacial Development and Tissue Biology, Tohoku University Graduate School of Dentistry, Sendai, 980-8575, Japan.
Division of Craniofacial Development and Tissue Biology, Tohoku University Graduate School of Dentistry, Sendai, 980-8575, Japan.
J Oral Biosci. 2019 Sep;61(3):149-156. doi: 10.1016/j.job.2019.07.004. Epub 2019 Aug 7.
Bone, dentin, and enamel are tissues formed through calcification, a process involving deposition of calcium phosphate minerals on extracellular organic matrices. Calcification, the underlying mechanism of which is unknown, is initiated with mineral deposition followed by advancing of the deposit and subsequent maturation of the mineral crystal.
We have reviewed the current knowledge of how calcification proceeds during bone development, bone healing, and enamel and dentin development, based on reported studies. Previous studies reported by us and by other authors have suggested that degradation of some extracellular matrix (ECM) proteins is involved in calcification during bone and dentin development and bone healing in a manner similar to that previously reported for enamel development.
The ECM proteins may inhibit mineral deposition and calcification, similar to the role of amelogenin during enamel development. The candidates for the amelogenin equivalents in bone and dentin have not been identified. Further studies are required to elucidate the regulatory mechanisms of bone and dentin calcification in light of specific ECM proteins that prevent calcification and enzymes that degrade these ECM proteins.
骨骼、牙本质和牙釉质是通过钙化形成的组织,钙化过程涉及磷酸钙矿物质在细胞外有机基质上的沉积。钙化的潜在机制尚不清楚,它始于矿物质沉积,随后是沉积物的推进以及矿物质晶体的成熟。
基于已发表的研究,我们回顾了目前关于骨骼发育、骨愈合以及牙釉质和牙本质发育过程中钙化如何进行的知识。我们和其他作者之前发表的研究表明,某些细胞外基质(ECM)蛋白的降解在骨骼和牙本质发育以及骨愈合过程中的钙化中起作用,其方式与之前报道的牙釉质发育情况类似。
ECM蛋白可能抑制矿物质沉积和钙化,类似于釉原蛋白在牙釉质发育中的作用。骨骼和牙本质中釉原蛋白类似物的候选者尚未确定。需要进一步研究,以根据防止钙化的特定ECM蛋白和降解这些ECM蛋白的酶来阐明骨骼和牙本质钙化的调节机制。