Toyosawa S, Kanatani N, Shintani S, Kobata M, Yuki M, Kishino M, Ijuhin N, Komori T
Department of Oral Pathology, Osaka University Graduate School of Dentistry, Suita, Osaka 565-0871, Japan.
Bone. 2004 Aug;35(2):553-61. doi: 10.1016/j.bone.2004.03.030.
Dentin matrix protein 1 (DMP1) is one of the acidic phosphorylated extracellular matrix proteins called the SIBLING (small integrin-binding ligand, N-linked glycoproteins) family. Recent studies showed that DMP1 is expressed in the mineralized tissues and suggested that DMP1 is involved in the mineralization. We investigated the precise localization of DMP1 messenger RNA (mRNA) and protein during fracture healing. In situ hybridization demonstrated that DMP1 mRNA was strongly expressed in preosteocytes and osteocytes in the bony callus during intramembranous and endochondral ossification while DMP1 mRNA was not detected in osteoblasts and chondrocytes. During endochondral ossification, however, a low number of DMP1-expressing cells were identified in the cluster of hypertrophic chondrocytes. However, these DMP1-expressing cells were not hypertrophic and were likely to be osteoblast-lineage cells, which were embedded in the matrix of bone or cartilage, because type I collagen-expressing cells and invasion of capillary vessels were observed in the same area. Northern blot, in situ hybridization, and immunohistochemical analyses showed that DMP1 mRNA and protein expressions were increased until day 14 postfracture, when bony callus was formed, and then declined to a lower level during remodeling of the bony callus. Therefore, DMP1 is likely to play an important role in the mineralization of the bony callus.
牙本质基质蛋白1(DMP1)是一种酸性磷酸化细胞外基质蛋白,属于SIBLING(小整合素结合配体,N-连接糖蛋白)家族。最近的研究表明,DMP1在矿化组织中表达,并提示DMP1参与矿化过程。我们研究了骨折愈合过程中DMP1信使核糖核酸(mRNA)和蛋白的精确定位。原位杂交显示,在膜内成骨和软骨内成骨过程中,骨痂中的前成骨细胞和骨细胞强烈表达DMP1 mRNA,而成骨细胞和软骨细胞中未检测到DMP1 mRNA。然而,在软骨内成骨过程中,在肥大软骨细胞簇中鉴定出少量表达DMP1的细胞。然而,这些表达DMP1的细胞并非肥大细胞,可能是成骨细胞系细胞,它们嵌入骨或软骨基质中,因为在同一区域观察到了表达I型胶原的细胞和毛细血管的侵入。Northern印迹、原位杂交和免疫组织化学分析表明,DMP1 mRNA和蛋白表达在骨折后第14天骨痂形成时增加,然后在骨痂重塑过程中下降到较低水平。因此,DMP1可能在骨痂矿化中起重要作用。