Nakamura O, Gohda E, Ozawa M, Senba I, Miyazaki H, Murakami T, Daikuhara Y
Calcif Tissue Int. 1985 Sep;37(5):491-500. doi: 10.1007/BF02557832.
A monoclonal antibody was raised against phosphophoryn, a unique noncollagenous phosphoprotein in dentin. Mouse myeloma NS-I cells were fused with spleen cells obtained from BALB/c mice immunized with phosphophoryn from fetal calf tooth germs. Mice inoculated with the hybridoma produced ascites fluid containing the antibody and this reacted only with a band of phosphophoryn transblotted from polyacrylamide gel. Immunohistochemical studies with the antibody showed that phosphophoryn was present in odontoblasts, odontoblastic processes and dentin, but not in the matrix of predentin, and that the phosphophoryn content of the dentin layer was high at and around the predentin-dentin junction and gradually decreased toward the enamel layer. The area corresponding to mantle dentin was not stained with the antibody.
制备了一种针对磷蛋白的单克隆抗体,磷蛋白是牙本质中一种独特的非胶原蛋白磷蛋白。将小鼠骨髓瘤NS-I细胞与从用胎牛牙胚磷蛋白免疫的BALB/c小鼠获得的脾细胞融合。接种杂交瘤的小鼠产生了含有该抗体的腹水,且该腹水仅与从聚丙烯酰胺凝胶转印的磷蛋白条带发生反应。用该抗体进行的免疫组织化学研究表明,磷蛋白存在于成牙本质细胞、成牙本质细胞突起和牙本质中,但前期牙本质基质中不存在,并且牙本质层的磷蛋白含量在前期牙本质-牙本质交界处及其周围较高,并朝着釉质层逐渐降低。与罩牙本质相对应的区域未被该抗体染色。